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10241-05-1

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10241-05-1 Usage

Physical Properties

Greenish-black monoclinic crystals or dark red as liquid or vapor; paramagnetic; hygroscopic; critical temperature 577°C; critical volume 369 cm3/mol; soluble in dry ether, dry alcohol and many other organic solvents; reacts with water.

Preparation

Molybdenum pentachloride may be prepared by heating molybdenite in chlorine. Sulfur chloride formed in the reaction is removed by distillation: 2MoS2 + 7Cl2 → 2MoCl5 + 2S2Cl2 Also, the compound may be prepared by the action of chlorine on molybdenum metal at elevated temperatures (500°C): 2Mo + 5Cl2 → 2MoCl5 The pentachloride may be obtained from the tetrachloride, MoCl4. The latter, when heated in a sealed tube sublimes, and upon cooling, disproportionates to MoCl5 and the trichloride, MoCl3: 2MoCl4 → MoCl5 + MoCl3

Chemical Properties

Green-black solid, dark red as liquid orvapor.Hygroscopic,reacting with water and air. Soluble in dry ether,dry alcohol, and other organic solvents.

Uses

Different sources of media describe the Uses of 10241-05-1 differently. You can refer to the following data:
1. Chlorination catalyst, vapor-deposited molyb-denum coatings, component of fire-retardant resins,brazing and soldering flux, intermediate fororganometallic compounds, e.g., molybdenum hex-acarbonyl.
2. Molybdenum pentachloride (MoCl5) is used as a brazing and soldering flux and to make fire-retardant resins.
3. Molybdenum pentachloride MoCl5 is used as a catalyst for several polymerization reactions involving olefins, vinyl monomers, trioxane, ethylene, vinylcyclohexane, cyclopentene, and butadiene.

Air & Water Reactions

MOLYBDENUM(V) CHLORIDE may react with water to produce corrosive hydrochloric acid and toxic fumes.

Reactivity Profile

MOLYBDENUM(V) CHLORIDE is a corrosive, hygroscopic solid, on contact with water or steam MOLYBDENUM(V) CHLORIDE decomposes to form hydrochloric acid. When heated to decomposition MOLYBDENUM(V) CHLORIDE emits toxic fumes of molybdenum chlorides and metallic molybdenum [Lewis, 3rd ed., 1993, p. 892]. Explodes on contact with finely divided sodium [Berry D. H., Chem. Eng. News, 1989, 67(47), p. 2]. Reaction with finely divided sodium sulfide is violent, may lead to autoignition [Kaner, R. B., Nature, 1991, 349, p. 510].

Hazard

Irritant.

Health Hazard

TOXIC; inhalation, ingestion or contact (skin, eyes) with vapors, dusts or substance may cause severe injury, burns or death. Contact with molten substance may cause severe burns to skin and eyes. Reaction with water or moist air will release toxic, corrosive or flammable gases. Reaction with water may generate much heat that will increase the concentration of fumes in the air. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Combustible material: may burn but does not ignite readily. Substance will react with water (some violently) releasing flammable, toxic or corrosive gases and runoff. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapors may travel to source of ignition and flash back. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated or if contaminated with water.

Safety Profile

A poison. A corrosive irritant to skin, eyes, and mucous membranes. Reacts with moisture to form hydrochloric acid. When heated to decomposition it emits toxic fumes of Mo and Cl-.

Check Digit Verification of cas no

The CAS Registry Mumber 10241-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,4 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10241-05:
(7*1)+(6*0)+(5*2)+(4*4)+(3*1)+(2*0)+(1*5)=41
41 % 10 = 1
So 10241-05-1 is a valid CAS Registry Number.
InChI:InChI=1/5ClH.Mo/h5*1H;/q;;;;;+5/p-5/rCl5Mo/c1-6(2,3,4)5

10241-05-1 Well-known Company Product Price

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  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (11832)  Molybdenum(V) chloride, 99.6% (metals basis)   

  • 10241-05-1

  • 5g

  • 387.0CNY

  • Detail
  • Alfa Aesar

  • (11832)  Molybdenum(V) chloride, 99.6% (metals basis)   

  • 10241-05-1

  • 50g

  • 1150.0CNY

  • Detail
  • Alfa Aesar

  • (11832)  Molybdenum(V) chloride, 99.6% (metals basis)   

  • 10241-05-1

  • 250g

  • 4509.0CNY

  • Detail
  • Alfa Aesar

  • (11832)  Molybdenum(V) chloride, 99.6% (metals basis)   

  • 10241-05-1

  • 1kg

  • 20248.0CNY

  • Detail
  • Aldrich

  • (208353)  Molybdenum(V)chloride  95%

  • 10241-05-1

  • 208353-25G

  • 637.65CNY

  • Detail
  • Aldrich

  • (208353)  Molybdenum(V)chloride  95%

  • 10241-05-1

  • 208353-100G

  • 2,231.19CNY

  • Detail
  • Aldrich

  • (642452)  Molybdenum(V)chloride  anhydrous, powder, 99.99% trace metals basis (excluding W)

  • 10241-05-1

  • 642452-2G

  • 866.97CNY

  • Detail
  • Aldrich

  • (642452)  Molybdenum(V)chloride  anhydrous, powder, 99.99% trace metals basis (excluding W)

  • 10241-05-1

  • 642452-10G

  • 3,079.44CNY

  • Detail

10241-05-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name molybdenum pentachloride

1.2 Other means of identification

Product number -
Other names Molybdenum(V) chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10241-05-1 SDS

10241-05-1Synthetic route

chlorine
7782-50-5

chlorine

molybdenum
7439-98-7

molybdenum

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
dry chlorine was passed over finely divided molebdenum at 300°C; sublimation;88%
at elevated temp.;
exotermic; reversible react. in zone at 1400 °C;
perfluoropropylene
116-15-4

perfluoropropylene

molybdenum(VI) oxide

molybdenum(VI) oxide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
by heating;
by heating;
sulfur dichloride
10545-99-0

sulfur dichloride

molybdenum(VI) oxide

molybdenum(VI) oxide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
reduced pressure, 160-180°C, 10h;
molybdenum(VI) oxide

molybdenum(VI) oxide

A

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

B

molybdenum(VI) tetrachloride oxide
55171-05-6, 13814-75-0

molybdenum(VI) tetrachloride oxide

C

dioxomolybdenum(VI) dichloride
13637-68-8

dioxomolybdenum(VI) dichloride

Conditions
ConditionsYield
With chlorine in presence of C (C:MoO3=3:1), start at 80°C: 190-600°C;
molybdenum(VI) oxide

molybdenum(VI) oxide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
With chlorine in presence of C; above 600°C (>18 l/h); C:MoO3 = 4:1;
With tetrachloromethane at 400°C;
With chlorine in presence of C (C:MoO3=3:1), start at 80°C: above 600°C;
With tetrachloromethane at 400°C;
tetrachlorosilane
10026-04-7, 53609-55-5

tetrachlorosilane

molybdenum(VI) oxide

molybdenum(VI) oxide

A

molybdenum(VI) oxide chloride

molybdenum(VI) oxide chloride

B

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

C

dioxomolybdenum(VI) dichloride
13637-68-8

dioxomolybdenum(VI) dichloride

Conditions
ConditionsYield
In neat (no solvent) byproducts: Cl2; heating of SiCl4 and MoO3 in a closed tube at 260-270°C;;
tetrachloromethane
56-23-5

tetrachloromethane

molybdenum(VI) oxide

molybdenum(VI) oxide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
In neat (no solvent) passing steam of CCl4 over MoO3 at 510 °C;;
In neat (no solvent) heating of MoO3 with CCl4 at about 280°C in a closed tube for 3 hours;;
In neat (no solvent) react. of MoO3 with CCl4 vapor at 510°C in absence of air;;
phosphorus pentachloride
10026-13-8, 874483-75-7

phosphorus pentachloride

molybdenum(VI) oxide

molybdenum(VI) oxide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
In neat (no solvent) heating of a mixt. of MoO3 and PCl5 in CO2-atm.; vigorous react. with formation of white and brown vapors;;
hydrogenchloride
7647-01-0

hydrogenchloride

molybdenum(VI) oxide

molybdenum(VI) oxide

A

oxomolybdenum(V) chloride
13814-74-9

oxomolybdenum(V) chloride

B

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

C

chlorine
7782-50-5

chlorine

D

molybdenum(VI) tetrachloride oxide
55171-05-6, 13814-75-0

molybdenum(VI) tetrachloride oxide

E

dioxomolybdenum(VI) dichloride
13637-68-8

dioxomolybdenum(VI) dichloride

Conditions
ConditionsYield
In solid byproducts: H2O; thermal decomposition of mixt. of MoO3 with poly(vinylchloride) or cerechlor 70 with different mole ratios in air, the heating rate of 10 deg/min at 20-850°C;
chlorine
7782-50-5

chlorine

molybdenum(VI) oxide

molybdenum(VI) oxide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
In tetrachloromethane heating of MoO3 with a dry soln. of Cl2 in CCl4 at 240°C in a closed tube for 3 hours;; crystn.; washing with CCl4 in CO2-atm.; sucking off; drying in vac.;;>99
In tetrachloromethane heating of MoO3 with a dry soln. of Cl2 in CCl4 at 240°C in a closed tube for 3 hours;; crystn.; washing with CCl4 in CO2-atm.; sucking off; drying in vac.;;>99
oxygen
80937-33-3

oxygen

chlorine
7782-50-5

chlorine

molybdenum
7439-98-7

molybdenum

A

molybdenum(VI) oxychloride

molybdenum(VI) oxychloride

B

molybdenum(VI) oxide chloride

molybdenum(VI) oxide chloride

C

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

chlorine
7782-50-5

chlorine

molybdenum
7439-98-7

molybdenum

A

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

B

molybdenum(IV) chloride
13320-71-3

molybdenum(IV) chloride

Conditions
ConditionsYield
In neat (no solvent) introduction of Cl2-gas (8-9 Torr/20 min/1.8 l/h) through purified (90min/H2 stream/1000°C) Mo powder (860 - 1160°C);; extraction of MoCl5 (CCl4); extraction MoCl4 (diethylether or water); further extraction (ethanol or water);;A n/a
B 0-10
molybdenum(IV) oxide

molybdenum(IV) oxide

A

molybdenum(II) chloride

molybdenum(II) chloride

B

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
With pyrographite In neat (no solvent)
With coal In neat (no solvent)
tetrachloromethane
56-23-5

tetrachloromethane

molybdenum(IV) oxide

molybdenum(IV) oxide

A

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

B

molybdenum(IV) chloride
13320-71-3

molybdenum(IV) chloride

Conditions
ConditionsYield
With pyrographite mass ratio MoO2:C = 5:1; mixt. heated at 300°C in a flow of N2 loaded with CCl4; absence of moisture and oxygen; further by-product: Mo oxide chloride; removal of MoCl5 and Mo oxide chloride by vac. distn.;A <1
B n/a
molybdenum(IV) oxide

molybdenum(IV) oxide

chlorine
7782-50-5

chlorine

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
With pyrographite In neat (no solvent) passing dry air-free Cl2 over a mixt. of MoO2 and coal at very high temp.;;
With coal In neat (no solvent) passing dry air-free Cl2 over a mixt. of MoO2 and coal at very high temp.;;
molybdenum(VI) fluoride
7783-77-9

molybdenum(VI) fluoride

phosphorus trichloride
7719-12-2, 52843-90-0

phosphorus trichloride

A

phosphorus pentachloride
10026-13-8, 874483-75-7

phosphorus pentachloride

B

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

C

trifluorophosphane
7783-55-3

trifluorophosphane

Conditions
ConditionsYield
In not given react. of an excess of PCl3 with MoF6 forming PF3, MoCl5, Cl2; further react. of an excess of PCl3 with Cl2 forming PCl5;;
In not given react. of an excess of PCl3 with MoF6 forming PF3, MoCl5, Cl2; further react. of an excess of PCl3 with Cl2 forming PCl5;;
MoCl5*POCl3
31438-02-5

MoCl5*POCl3

A

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
In neat (no solvent) decompn. on heating at about 170°C;;
In neat (no solvent) decompn. on heating at about 170°C;;
tetrachloromethane
56-23-5

tetrachloromethane

Mo3O8

Mo3O8

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
In neat (no solvent) react. of Mo3O8 and CCl4 at 240°C;;
In neat (no solvent) react. of Mo3O8 and CCl4 at 240°C;;
molybdenite

molybdenite

chlorine
7782-50-5

chlorine

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
In neat (no solvent) react. of MoS2 and Cl2 at high temp.;;
In neat (no solvent) react. of MoS2 and Cl2 at high temp.;;
tetrachloromethane
56-23-5

tetrachloromethane

molybdenum(IV) oxide

molybdenum(IV) oxide

molybdenum(IV) chloride
13320-71-3

molybdenum(IV) chloride

B

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
With C In neat (no solvent) byproducts: Mo-oxychloride; heating of MoO2 and carbon in N2-stream satd. with CCl4 (<300°C); sublimation off of MoCl5 (vac., 100°C);
With C In neat (no solvent) heating of MoO2 and carbon in N2-stream satd. with CCl4 (300°C, 2h); sublimation off of MoCl5 (vac., 100°C); elem. anal.;
molybdenum(V) oxide

molybdenum(V) oxide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
With hydrogenchloride 200°C;
With HCl 200°C;
thionyl chloride
7719-09-7

thionyl chloride

molybdenum acid

molybdenum acid

nonachlorodimolybdenum(V) heptachlorodioxodimolybdate(V)

nonachlorodimolybdenum(V) heptachlorodioxodimolybdate(V)

B

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

C

dioxomolybdenum(VI) dichloride
13637-68-8

dioxomolybdenum(VI) dichloride

Conditions
ConditionsYield
In neat (no solvent) reflux for 96 h; removal of excess thionyl chloride, vacuum sublimation;
trans-(Et2O)2MoCl4
30411-56-4

trans-(Et2O)2MoCl4

A

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

B

molybdenum(III) chloride
13478-18-7

molybdenum(III) chloride

Conditions
ConditionsYield
In neat (no solvent) heating under vac. above 140°C;
molybdenum (IV) sulfide

molybdenum (IV) sulfide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
With chlorine In neat (no solvent) chemical transport reaction (900 to 800°C);;
molybdenum(IV) chloride
13320-71-3

molybdenum(IV) chloride

A

molybdenum(II) chloride

molybdenum(II) chloride

B

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

C

molybdenum(III) chloride
13478-18-7

molybdenum(III) chloride

Conditions
ConditionsYield
In neat (no solvent) heating of MoCl4 in a closed tube;;
In neat (no solvent) heating of MoCl4 in a closed tube;;
molybdenum(IV) chloride
13320-71-3

molybdenum(IV) chloride

A

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

B

molybdenum(III) chloride
13478-18-7

molybdenum(III) chloride

Conditions
ConditionsYield
In ethanol decompn. of MoCl4 on solving in alc.;;
In diethyl ether decompn. of MoCl4 on solving in ether;;
In neat (no solvent) thermal decomposition of MoCl4 in vac. or under Ar in a sealed ampoule;
molybdenite

molybdenite

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

Conditions
ConditionsYield
With chlorine In neat (no solvent) passing Cl2 over heated MoS2;;
With chlorine In neat (no solvent) react. of MoS2 in a stream of chlorine;;
With Cl2 In neat (no solvent) react. of MoS2 in a stream of chlorine;;
With Cl2 In neat (no solvent) passing Cl2 over heated MoS2;;
sodium azide

sodium azide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

molybdenum nitride

molybdenum nitride

Conditions
ConditionsYield
In neat (no solvent) High Pressure; all manipulations carried out in a dry glove box with Ar flowing; MoCl5 and NaN3 placed into a stainless steel autoclave; sealed and heated for 12 h at the temp. of 450, 500, and 550°C, respectively, followed by cooling to room temp. on standing; product washed with dilute absolute ethanolic dilute HCl and distilled water for several times; vacuum-dried at 60°C for 4 h;100%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

[MoCl4(NSCl)OPCl3]
87142-29-8

[MoCl4(NSCl)OPCl3]

Conditions
ConditionsYield
With thiazyl chloride In neat (no solvent) MoCl5 is dissolved in POCl3. The resulting soln. is added within 0.5 h to a soln. of S3N3Cl3 under stirring and cooling with an ice bath (underdry conditions).; After 2 h POCl3 is pumped off in vacuo for 5 h; elem. anal.;100%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

diphenyl acetylene
501-65-5

diphenyl acetylene

{MoCl4(PhCCPh)}2

{MoCl4(PhCCPh)}2

Conditions
ConditionsYield
In dichloromethane under exclusion of O2 and moisture in pure Ar; to a suspn. of MoCl5 in CH2Cl2 is added diphenylacetylene under stirring (2 d, room temp.); filtn., washed with CH2Cl2, dried in vacuum, elem. anal.;99%
With C2Cl4
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

MoOCl3(NC5H5)3
79803-20-6

MoOCl3(NC5H5)3

Conditions
ConditionsYield
With pyridine In pyridine 6 h stirring; filtration, elem. anal.;99%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

molybdenum
7439-98-7

molybdenum

Conditions
ConditionsYield
With magnesium hydride In toluene byproducts: H2; (argon); grinding MoCl5 and MgH2 in a mill, addn. of toluene, heating toreflux temp. under further grinding (9 h); washing (toluene), drying (vac.);97.6%
With hydrogen
on annealing single crystal tungsten wire, in MoCl5-WCl6 gas mixt. normal mixed crystal formation;
Hexamethyldisiloxane
107-46-0

Hexamethyldisiloxane

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

molybdenum oxide trichloride

molybdenum oxide trichloride

Conditions
ConditionsYield
In dichloromethane byproducts: Me3SiCl; under inert atm.; soln. of Si-compd. added dropwise to a stirred suspension of Mo-compd. at room temp. , mixt. stirred at room temp. for 2h, dark brown solid and colorless soln.; supernatant decanted, solid collected, washed (light petroleum), dried (vac.); elem. anal.;97.5%
1,4-diphenyl-1,3-butadiyne
886-66-8

1,4-diphenyl-1,3-butadiyne

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

{MoCl4(C6H5CCCCC6H5)}2

{MoCl4(C6H5CCCCC6H5)}2

Conditions
ConditionsYield
In tetrachloromethane byproducts: PhC4Cl2Ph; to a suspn. of MoCl5 in CCl4 is added a soln. of PhCCCCPh in CCl4 with stirring, soln. is stirred for 6 d; ppt. is filtered, washed with CCl4 and dried in vac., elem. anal.;97%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

[Cl2OMo(μ-OC2H5)2(μHOC2H5)MoOCl2]

[Cl2OMo(μ-OC2H5)2(μHOC2H5)MoOCl2]

Conditions
ConditionsYield
With C2H5OH In ethanol; chloroform under N2; a mixt. of CHCl3 and EtOH is added to MoCl5, stirred; the volatiles are evapd. in vac., the ppt. is washed, elem. anal.;97%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

acetonitrile
75-05-8

acetonitrile

bis(acetonitrile)tetrachloromolybdenum(IV)
56613-96-8, 77210-60-7, 15584-93-7, 19187-82-7

bis(acetonitrile)tetrachloromolybdenum(IV)

Conditions
ConditionsYield
at 20℃; for 14h; Inert atmosphere; Schlenk technique;96%
at 20℃; for 20.3333h; Inert atmosphere;93%
In acetonitrile solid MoCl5 added to MeCN, stirred for 3 h at ambient temp.; filtered, washed with MeCN, dried in vac.;87%
dimethylbis(phenylethynyl)silane
2170-08-3

dimethylbis(phenylethynyl)silane

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

2Mo(4+)*8Cl(1-)*C6H5CCSi(CH3)2CCC6H5=[Mo2Cl8(C6H5CCSi(CH3)2CC(C6H5))]

2Mo(4+)*8Cl(1-)*C6H5CCSi(CH3)2CCC6H5=[Mo2Cl8(C6H5CCSi(CH3)2CC(C6H5))]

Conditions
ConditionsYield
In tetrachloromethane byproducts: PhC2Cl2SiMe2C2Cl2; under Ar; adding slowly dropwise a soln. of PhCCSiMe2CCPh to a suspn. of MoCl5, stirring (2 d, room temp.); filtering, washing (CCl4), drying (high vac.); elem. anal.;96%
bis(trichlorophosphine)iminium chloride

bis(trichlorophosphine)iminium chloride

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

bis(trichlorophosphine)iminium hexachloromolybdate(V)
116591-43-6

bis(trichlorophosphine)iminium hexachloromolybdate(V)

Conditions
ConditionsYield
In dichloromethane exclusion of moisture, stirred for 12 h at room temp.; pptd. with CCl4, filtered, washed with CCl4, dried in vac.; elem. anal.;95%
N-trimethylsilyl(triphenylphosphoranylidene)amine
13892-06-3

N-trimethylsilyl(triphenylphosphoranylidene)amine

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

{MoCl4(NP(C6H5)3)}2*CH2Cl2

{MoCl4(NP(C6H5)3)}2*CH2Cl2

Conditions
ConditionsYield
With CH2Cl2 In dichloromethane byproducts: ClSi(CH3)3; slow addn. of phosphorane soln. to MoCl5 suspension with stirring, excluding moisture; refluxing, 3h; cooling; pptn.; filtration; washing (CH2Cl2); drying (vac.) for a short period of time; elem. anal.;95%
Di-n-butyl selenide
14835-66-6

Di-n-butyl selenide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

acetonitrile
75-05-8

acetonitrile

trans-[MoCl4(nBu2Se)2]

trans-[MoCl4(nBu2Se)2]

Conditions
ConditionsYield
Stage #1: molybdenum(V) chloride; acetonitrile for 0.5h; Inert atmosphere; Schlenk technique;
Stage #2: Di-n-butyl selenide In dichloromethane for 0.25h; Inert atmosphere; Schlenk technique;
94%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

2-aminobenzothiazole hydrochloride
94787-08-3

2-aminobenzothiazole hydrochloride

2C7H7N2S(1+)*MoOCl5(2-)=(C7H7N2S)2{MoOCl5}

2C7H7N2S(1+)*MoOCl5(2-)=(C7H7N2S)2{MoOCl5}

Conditions
ConditionsYield
In hydrogenchloride Addn. of ligand to soln. of MoCl5.; Concg., cooling in ice, passing a stream of HCl through the soln., green crystals ppt., washing (ether, thionyl chloride), drying over KOH, elem. anal.;92%
1,2-dimethoxyethane
110-71-4

1,2-dimethoxyethane

Hexamethyldisiloxane
107-46-0

Hexamethyldisiloxane

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

MoOCl3(CH3OCH2CH2OCH3)
14523-42-3, 141778-40-7

MoOCl3(CH3OCH2CH2OCH3)

Conditions
ConditionsYield
In dichloromethane addn. of Me3SiOSiMe3 to a soln. of W-complex in CH2Cl2 and 1,2-dimethoxyethane, stirring for a short period; filtn., elem. anal.;91%
P(C6H5)4(1+)*MoNCl4(1-) = P(C6H5)4MoNCl4
89087-28-5, 94930-25-3

P(C6H5)4(1+)*MoNCl4(1-) = P(C6H5)4MoNCl4

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

2P(C6H5)4(1+)*{Mo2NCl9}2(2-) = (P(C6H5)4)2{Mo2NCl9}2

2P(C6H5)4(1+)*{Mo2NCl9}2(2-) = (P(C6H5)4)2{Mo2NCl9}2

Conditions
ConditionsYield
With POCl3; Cl2 In dichloromethane exclusion of moisture; a soln. of the Mo-complex is dropped into a suspension of MoCl5 with stirring, stirring continued for further 12 h;; filtration; washing (CH2Cl2); drying in vac.; a second crop is obtained by concn. of the filtrate; elem. anal.;90%
[2,2]bipyridinyl
366-18-7

[2,2]bipyridinyl

2,2-dimethylpropylidynephosphine
78129-68-7

2,2-dimethylpropylidynephosphine

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

{MoCl2(C5H4NC5H4N)2(1+)}*{MoCl4(C5H4NC5H4N)(1-)}={Mo2Cl6(C5H4NC5H4N)3}

{MoCl2(C5H4NC5H4N)2(1+)}*{MoCl4(C5H4NC5H4N)(1-)}={Mo2Cl6(C5H4NC5H4N)3}

Conditions
ConditionsYield
In dichloromethane byproducts: Me3C-CC-CMe3; filtered, the filtration cooled at 5°C, filtered, elem. anal.;90%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

MoCl4(NSCl)
94017-24-0

MoCl4(NSCl)

Conditions
ConditionsYield
With thiazyl chloride In dichloromethane byproducts: Cl2; MoCl5 is suspd. in CH2Cl2, heated to 35°C and S3N3Cl3 in CH2Cl2 is added under stirring (under dry conditions). The color changes from dark red to dark violett after 0.5 h.; After 20 h filtn., washing with CH2Cl2 and drying in vavuo; elem. anal.;90%
bis(trichlorophosphine)iminium hexachlorophosphate
18828-06-3

bis(trichlorophosphine)iminium hexachlorophosphate

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

A

bis(trichlorophosphine)iminium hexachloromolybdate(V)
116591-43-6

bis(trichlorophosphine)iminium hexachloromolybdate(V)

B

phosphorus pentachloride
10026-13-8, 874483-75-7

phosphorus pentachloride

Conditions
ConditionsYield
In not given exclusion of moisture, stirred for 12 h at room temp.; filtered, dissolved in CH2Cl2, pptd. with CCl4, filtered, washed with CCl4, dried in vac.; elem. anal.;A 89%
B n/a
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

trans-bisdinitrogenbis(1,2-diphenylphosphinoethane)molybdenum(0)

trans-bisdinitrogenbis(1,2-diphenylphosphinoethane)molybdenum(0)

Conditions
ConditionsYield
With nitrogen; 1,2-bis-(diphenylphosphino)ethane In tetrahydrofuran Electrochem. Process; MoCl5-Ph2PCH2CH2PPh2 in THF-NBu4BF4 was electrolysed under N2 (20°C, 1 atm) (E(app)=-2.4 V); mechanism discussed;; catholyte was removed, THF was removed under vac. at room temp. left a mixt. of product and NBu4BF4, soluble in CH3CN or MeOH, catholyte residue was repeated extd. with solvent, product was removed, recrystd. from Et2O-THF;89%
tetrahydrofuran
109-99-9

tetrahydrofuran

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

[MoCl4(tetrahydrofuran)2]
16998-75-7

[MoCl4(tetrahydrofuran)2]

Conditions
ConditionsYield
In tetrahydrofuran; diethyl ether under Ar; MoCl5 and Sn suspd. in Et2O at room temp., mixt. stirred for 30 min, excess Sn sepd. by transferring the gently stirred supernatant suspn. in a new flask, suspn. filtered, ppt. washed (Et2O), THF added, mixt. stirred for 3 h at room temp.; liquid decanted off, residue washed with THF and ether, dried in vac.;89%
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

tert-butylamine
75-64-9

tert-butylamine

bis-t-butylamidobis-t-butylaminebis-t-butylimidotetrachlorodimolybdenum(V)*1/6C6H6

bis-t-butylamidobis-t-butylaminebis-t-butylimidotetrachlorodimolybdenum(V)*1/6C6H6

Conditions
ConditionsYield
With benzene In benzene byproducts: Me3CNH3Cl; a soln. of the amine (43.9 mmol) in benzene is added to a suspn. of MoCl5 (7.3 mmol) in benzene and the mixt. stirred for 3 h; filtration, residue washed with benzene; filtrates combined and evapd; solid washed with petroleum ether and dried in vac.; elem. anal.;88%
trimethyl(tert-butylamino)silane
5577-67-3

trimethyl(tert-butylamino)silane

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

bis-t-butylaminebis-t-butylimidohexachlorodimolybdenum(V)*1/6C6H6

bis-t-butylaminebis-t-butylimidohexachlorodimolybdenum(V)*1/6C6H6

Conditions
ConditionsYield
With benzene In benzene a soln. of the amine (10.35 mmol) in benzene is slowly added to a suspn. of MoCl5 (5.1 mmol) in benzene cooled to ica-water temp.; mixt. stirred for 18 h; filtration, solid washed with benzene and dried in vac.; product is a mixt. of 2 isomers; elem. anal.;88%
(C6H5)3PCH3(1+)*{MoNCl4}(1-)=((C6H5)3PCH3){MoNCl4}
85361-08-6

(C6H5)3PCH3(1+)*{MoNCl4}(1-)=((C6H5)3PCH3){MoNCl4}

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

(C6H5)3PCH3(1+)*{Mo2NCl9}(1-)=((C6H5)3PCH3){Mo2NCl9}

(C6H5)3PCH3(1+)*{Mo2NCl9}(1-)=((C6H5)3PCH3){Mo2NCl9}

Conditions
ConditionsYield
In dichloromethane stirring, room temp., 2h; pptn.; filtration; washing (CH2Cl2); drying (vac.); elem. anal.;88%
In dichloromethane; benzene addn. of Mo complex soln. (CH2Cl2) to MoCl5 soln. (benzene); pptn. of oil; crystn. within one day; filtration; washing (CH2Cl2); drying (vac.); elem. anal.;
molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

silicon tetraiodide
13465-84-4

silicon tetraiodide

MoI3

MoI3

Conditions
ConditionsYield
at 150℃; for 16h; Inert atmosphere; Schlenk technique;88%
at 120℃; for 16h;
hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

molybdenum tetrabromide
13520-59-7

molybdenum tetrabromide

Conditions
ConditionsYield
In further solvent(s) cooling MoCl5 in C2H5Br (red-brown soln.) to about -50°C; connecting to a vac. line and to a cylinder of HBr; introduction of HBr (colorless soln. after 10min, pptn.); repeating 5times vac./HBr operation, 2h; stirring, room temp., 15h;; filtration of black solid; washing with heptane; drying in vac.; elem. anal.;;87%
hexamethyldisilathiane
3385-94-2

hexamethyldisilathiane

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

molybdenum(V) sulphide trichloride

molybdenum(V) sulphide trichloride

Conditions
ConditionsYield
In dichloromethane byproducts: Me3SiCl; under inert atm.; suspension of Mo-compd. cooled in a dry-ice/acetone slush bath, treated dropwise over a period of 15 min with soln. of Si-compd. chilled to -30°C, pptn., mixt. allowed to warm to room temp., stirred for 2h; supernatant decanted, solid collected, washed (petroleum ether), dried (vac.); elem. anal.;87%
2,2-dimethylpropylidynephosphine
78129-68-7

2,2-dimethylpropylidynephosphine

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

methyltriphenylphosphonium chloride
1031-15-8

methyltriphenylphosphonium chloride

A

2((C6H5)3PCH3)(1+)*{MoCl6(2-)}=((C6H5)3PCH3)2{(MoCl6)}

2((C6H5)3PCH3)(1+)*{MoCl6(2-)}=((C6H5)3PCH3)2{(MoCl6)}

B

3((C6H5)3PCH3)(1+)*{(Mo2Cl9)(3-)}=((C6H5)3PCH3)3{(Mo2Cl9)}

3((C6H5)3PCH3)(1+)*{(Mo2Cl9)(3-)}=((C6H5)3PCH3)3{(Mo2Cl9)}

Conditions
ConditionsYield
In dichloromethane byproducts: Me3C-CC-CMe3; filtered, washed with CH2Cl2, CCl4 added to filtrate, pptd., elem. anal.;A 13%
B 87%
phosgene
75-44-5

phosgene

molybdenum(V) chloride
10241-05-1

molybdenum(V) chloride

tetramethylurea
632-22-4

tetramethylurea

3(N(CH3)2)2CCl(1+)*MoCl8(3-) = [(N(CH3)2)2CCl]3(MoCl8)

3(N(CH3)2)2CCl(1+)*MoCl8(3-) = [(N(CH3)2)2CCl]3(MoCl8)

Conditions
ConditionsYield
In toluene (N2); stirring (0°C); ppt. washing (CHCl3, Et2O), drying (vac.); elem. anal.;87%

10241-05-1Relevant articles and documents

Smith, E. F.,Burr, H. C.

, p. 578 - 578 (1894)

Westland, Alan D.,Uzelac, Vladimir

, p. L37 - L39 (1977)

Gutmann, V.,Mairinger, F.

, (1958)

Improved preparations of molybdenum coordination compounds from tetrachlorobis(diethyl ether)molybdenum(IV)

Stoffelbach, Fran?ois,Saurenz, Dirk,Poli, Rinaldo

, p. 2699 - 2703 (2007/10/03)

The reduction of MoCl5 with metallic tin in diethyl ether provides a rapid and convenient entry to [MoCl4(OEt2)2] This compound can be transformed easily and in high yields into a variety of other useful synthon

The Crystal Structure of Nonachlorodimolybdenum(V) Heptachlorodioxo-dimolybdate(V)

Edwards, Anthony J.,Slim, David R.

, p. 485 - 488 (2007/10/02)

The compound Mo2Cl8O was formed as a minor product in the reaction of molybdic acid with thionyl chloride.Its structure has been determined by the heavy-atom method from 1265 reflections, measured with a diffractometer, and refined by full-matrix least-squares methods to R 0.066.Crystals are monoclinic, space group P2/c, with a=10.01(1), b=6.27(1), c=17.89(2) Angstroem, β=101.8(3) grad.The structure consists of singly chlorine-bridged, binuclear cations + and triply chlorine-bridged binuclear anions - which are linked into chains by weak interactions through the oxygen atoms.

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