Welcome to LookChem.com Sign In|Join Free

CAS

  • or

644-97-3

Post Buying Request

644-97-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

644-97-3 Usage

Chemical Properties

Colorless to light yellow liqui

Uses

Different sources of media describe the Uses of 644-97-3 differently. You can refer to the following data:
1. Organic synthesis, for derivation of plasticizers, polymers, antioxidants; oil additives.
2. Dichlorophenylphosphine and its derivatives are used as an intermediate to make plasticizers, antioxidants, stabilizers, catalysts and high pressure lubricant additives and in lacquer formulatings.

General Description

A colorless, fuming liquid. Density 1.32 g / cm3. Flash point 102°C. Corrosive to metals and tissue.

Air & Water Reactions

Reacts with water, including moisture in air or soil, to liberate heat and hydrochloric acid [Merck, 11th ed. 1989].

Reactivity Profile

Dichlorophenylphosphine is incompatible with water, with bases (including amines), with strong oxidizing agents, and with alcohols. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291].

Hazard

Highly corrosive to skin, tissue. Flammable.

Health Hazard

Inhalation causes irritation of nose and throat; pulmonary edema may develop following severe exposures. Contact with skin or eyes causes severe burns. Ingestion causes severe burns of mouth and stomach.

Flammability and Explosibility

Nonflammable

Safety Profile

A poison irritant to skin, eyes, and mucous membranes and poison by ingestion and inhalation. When heated to decomposition it emits very toxic fumes of Cland POx. See also PHOSPHINE.

Purification Methods

Distil it in a vacuum byfractionating through a 20cm column packed with glass helices (better use a spinning band column) [Buchner & Lockhart J Am Chem Soc 73 755 1951, NMR: Müller et al. J Am Chem Soc 78 3557 1956, IR: Daasch & Smith Anal Chem 23 853 1951]. It forms a yellow Ni complex: Ni(C6H5Cl2P)4 (m 91-92o, from H2O) [Quin J Am Chem Soc 79 3681 1957 ] and a yellow complex with molybdenum carbonyl: Mo(CO)3.(C6H5Cl2P)3 (m 106-110o dec) [Abel et al. J Chem Soc 2323 1959]. [Beilstein 16 IV 972.]

Check Digit Verification of cas no

The CAS Registry Mumber 644-97-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,4 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 644-97:
(5*6)+(4*4)+(3*4)+(2*9)+(1*7)=83
83 % 10 = 3
So 644-97-3 is a valid CAS Registry Number.
InChI:InChI=1/2C6H7P.2ClH/c2*7-6-4-2-1-3-5-6;;/h2*1-5H,7H2;2*1H/p-2

644-97-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (A10284)  Dichlorophenylphosphine, 97%   

  • 644-97-3

  • 50g

  • 371.0CNY

  • Detail
  • Alfa Aesar

  • (A10284)  Dichlorophenylphosphine, 97%   

  • 644-97-3

  • 250g

  • 614.0CNY

  • Detail
  • Alfa Aesar

  • (A10284)  Dichlorophenylphosphine, 97%   

  • 644-97-3

  • 1000g

  • 1549.0CNY

  • Detail

644-97-3SDS

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 Dichlorophenylphosphine

1.2 Other means of identification

Product number -
Other names Phosphonous dichloride, phenyl-

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Process regulators
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:644-97-3 SDS

644-97-3Synthetic route

benzene
71-43-2

benzene

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With aluminium trichloride; phosphorus trichloride for 3h; Heating;96%
Stage #1: benzene With aluminum (III) chloride; phosphorus trichloride for 5h; Reflux; Sealed tube;
Stage #2: With trichlorophosphate In Petroleum ether for 1h; Concentration; Reflux; Sealed tube;
95.5%
With phosphorus trichloride for 2h; Time; Reflux;93.6%
chlorobenzene
108-90-7

chlorobenzene

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With phosphorus; phosphorus trichloride at 70 - 350℃; under 30003 Torr; for 6h; Concentration; Pressure; Temperature;94.35%
With phosphorus; phosphorus trichloride at 390℃;58.9%
With phosphorus; nickel; phosphorus trichloride at 390℃; Product distribution; other catalysts;33.1%
P,P-dichlorophenylphosphine oxide
824-72-6

P,P-dichlorophenylphosphine oxide

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With triphenylphosphine91%
triphenylphosphine
603-35-0

triphenylphosphine

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With phosphorus trichloride at 350℃; for 5h;85%
1,1,3,3-Tetrafluoro-4,6-bis-trifluoromethyl-1,3-dihydro-isobenzofuran

1,1,3,3-Tetrafluoro-4,6-bis-trifluoromethyl-1,3-dihydro-isobenzofuran

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With aluminium trichloride; phosphorus trichloride for 5h; Heating;84%
phenylphosphane
638-21-1

phenylphosphane

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With phosphorus pentachloride In diethyl ether at 20℃;83%
With phosphorus pentachloride In toluene
phenyltetrachlorophosphorane
4895-65-2

phenyltetrachlorophosphorane

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With tetraethylammonium iodide In benzene for 1h;79%
With phosphorous acid trimethyl ester; triethyl phosphite
phenyltrichlorophosphonium hexachlorophosphorate
55045-25-5

phenyltrichlorophosphonium hexachlorophosphorate

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With diethyl phosphorylchloridite In benzene for 6h; also with EtOPCl2;72%
With difluoro diethylamino phosphine In benzene for 0.5h;
With difluoro diethylamino phosphine In benzene for 0.5h; other substrates;
ethyl phenylphosphonochloridothioite
23588-02-5

ethyl phenylphosphonochloridothioite

cyclohexanone
108-94-1

cyclohexanone

A

chloroanhydride of phenyl-α-hydroxycyclohexylphosphinic acid
60340-72-9

chloroanhydride of phenyl-α-hydroxycyclohexylphosphinic acid

B

phenylphosphinic acid
1779-48-2

phenylphosphinic acid

C

C6H6ClOP
67176-71-0

C6H6ClOP

D

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With acetic acid at 0℃; for 240h;A 50%
B n/a
C n/a
D n/a
N,N-dimethylamino-P-phenyl-C-methylmethylenephosphine
75589-83-2

N,N-dimethylamino-P-phenyl-C-methylmethylenephosphine

benzenesulfenyl chloride
931-59-9

benzenesulfenyl chloride

A

S-phenyl-P-phenyldithiophosphonous chloride
26990-26-1

S-phenyl-P-phenyldithiophosphonous chloride

B

S,S-diphenyl-P-phenyldithiophosphonite
38476-60-7

S,S-diphenyl-P-phenyldithiophosphonite

C

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
In acetonitrileA n/a
B 20%
C n/a
benzene
71-43-2

benzene

A

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

B

chloro-diphenylphosphine
1079-66-9

chloro-diphenylphosphine

Conditions
ConditionsYield
With aluminium trichloride; phosphorus trichloride at 140 - 150℃; for 5h; Product distribution; Mechanism; var. temps; var. molar proportion of reactants; var. time;A 14%
B 20%
diphenylmercury(II)
587-85-9

diphenylmercury(II)

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With phosphorus trichloride at 180℃;
Tris(2-chloroethyl) phosphate
115-96-8

Tris(2-chloroethyl) phosphate

phenylphosphonous acid dichloride; compound with aluminium trichloride (1:1)
82123-74-8

phenylphosphonous acid dichloride; compound with aluminium trichloride (1:1)

A

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

B

complex of tris-2-chloroethyl phosphate with aluminum chloride

complex of tris-2-chloroethyl phosphate with aluminum chloride

Conditions
ConditionsYield
With phosphorus trichloride at 30℃; for 0.333333h; Product distribution; complexes of various arylphosphonous dichlorides with aluminum chloride;
phenyltetrachlorophosphorane
4895-65-2

phenyltetrachlorophosphorane

A

P,P-dichlorophenylphosphine oxide
824-72-6

P,P-dichlorophenylphosphine oxide

B

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With Diethyl phosphate In benzene for 1h; Product distribution; (C2H5O)2PONa;
phenyltetrachlorophosphorane
4895-65-2

phenyltetrachlorophosphorane

A

phenyl-β-chlorovinylphosphinic chloride
3135-58-8

phenyl-β-chlorovinylphosphinic chloride

B

phenyl-β-ethoxyvinylphosphinic chloride
90876-11-2

phenyl-β-ethoxyvinylphosphinic chloride

C

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With phosphan; ethyl vinyl ether Yield given. Multistep reaction. Yields of byproduct given;
diphenyl phenylphosphonite
13410-61-2

diphenyl phenylphosphonite

phenyl-phosphonochloridous acid phenyl ester
2171-93-9

phenyl-phosphonochloridous acid phenyl ester

A

triphenyl phosphite
101-02-0

triphenyl phosphite

B

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
at 140℃; Equilibrium constant;
C11H8ClF8OP
126215-38-1

C11H8ClF8OP

Phosphorochloridous acid bis-(2,2,3,3,4,4,5,5-octafluoro-pentyl) ester
126215-34-7

Phosphorochloridous acid bis-(2,2,3,3,4,4,5,5-octafluoro-pentyl) ester

A

tris(2,2,3,3,4,4,5,5-octafluoropentyl) phosphite
65611-17-8

tris(2,2,3,3,4,4,5,5-octafluoropentyl) phosphite

B

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
at 140℃; Equilibrium constant;
phenyltrichlorophosphonium hexachlorophosphorate
55045-25-5

phenyltrichlorophosphonium hexachlorophosphorate

A

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

B

triethylsulfonium dichloroiodate

triethylsulfonium dichloroiodate

Conditions
ConditionsYield
With triethylsulfonium iodide
phenyltetrachlorophosphorane
4895-65-2

phenyltetrachlorophosphorane

ethyl vinyl ether
109-92-2

ethyl vinyl ether

A

phenyl-β-chlorovinylphosphinic chloride
3135-58-8

phenyl-β-chlorovinylphosphinic chloride

B

phenyl-β-ethoxyvinylphosphinic chloride
90876-11-2

phenyl-β-ethoxyvinylphosphinic chloride

C

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With phosphan Yield given. Multistep reaction. Yields of byproduct given;
dichloromethylphenylsilane
149-74-6

dichloromethylphenylsilane

A

Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

B

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
With pyridine; aluminium trichloride; phosphorus trichloride 1) 80-90 deg C, 10 h, 2) reflux, 1 h; Yield given. Multistep reaction. Yields of byproduct given;
diphenylmercury(II)
587-85-9

diphenylmercury(II)

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

phosphorus trichloride

A

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

B

phenylmercury(II) chloride
100-56-1

phenylmercury(II) chloride

Conditions
ConditionsYield
at 180℃;
phosgene
75-44-5

phosgene

phenylphosphane
638-21-1

phenylphosphane

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

C

methylammonium carbonate
15719-64-9, 15719-76-3, 97762-63-5

methylammonium carbonate

aluminium trichloride
7446-70-0

aluminium trichloride

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

phosphorus trichloride

benzene
71-43-2

benzene

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
bei Siedetemperatur;
phenyltetrachlorophosphorane
4895-65-2

phenyltetrachlorophosphorane

A

chlorine
7782-50-5

chlorine

B

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
beim Erhitzen;
diethyl ether
60-29-7

diethyl ether

triphenylbismuthane
603-33-8

triphenylbismuthane

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

phosphorus trichloride

A

diphenylbismuth(III) chloride
5153-28-6

diphenylbismuth(III) chloride

B

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

C

chloro-diphenylphosphine
1079-66-9

chloro-diphenylphosphine

Conditions
ConditionsYield
reagiert analog mit Arsentrichlorid;
dibromo-dichloro-phenyl-phosphorane
81861-09-8

dibromo-dichloro-phenyl-phosphorane

A

1.4-dibromobenzene
106-37-6

1.4-dibromobenzene

B

hydrogen bromide
10035-10-6, 12258-64-9

hydrogen bromide

C

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

D

phosphorus halogen

phosphorus halogen

Conditions
ConditionsYield
at 150℃;
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

1,3-Dikalium-1,2,3-triphenyltriphosphid
6002-55-7

1,3-Dikalium-1,2,3-triphenyltriphosphid

A

CF3SP(Cl)C6H5
69646-22-6

CF3SP(Cl)C6H5

B

(CF3S)2PC6H5
69646-19-1

(CF3S)2PC6H5

C

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

Conditions
ConditionsYield
In tetrahydrofuran at -50 to 20°C;
In tetrahydrofuran
Trifluoromethylsulfenyl chloride
421-17-0

Trifluoromethylsulfenyl chloride

pentaphenylcyclopentaphosphane
3376-52-1

pentaphenylcyclopentaphosphane

A

CF3SP(Cl)C6H5
69646-22-6

CF3SP(Cl)C6H5

B

(CF3S)2PC6H5
69646-19-1

(CF3S)2PC6H5

C

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

ethanol
64-17-5

ethanol

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

ethyl Phenylphosphinate
172487-18-2

ethyl Phenylphosphinate

Conditions
ConditionsYield
In diethyl ether at 20℃; for 0.5h; Arbuzov reaction;100%
In tetrahydrofuran at 0 - 20℃; for 20h; Inert atmosphere; Schlenk technique;95%
In tetrahydrofuran at 0℃;90%
triflic azide
3855-45-6

triflic azide

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

CF3SO2NPCl2C6H5
30227-07-7

CF3SO2NPCl2C6H5

Conditions
ConditionsYield
100%
(-)-menthol
2216-51-5

(-)-menthol

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

(-)-(o-menthyl)chlorophenylphosphine

(-)-(o-menthyl)chlorophenylphosphine

Conditions
ConditionsYield
Stage #1: (-)-menthol With n-butyllithium In tetrahydrofuran; hexane at 0℃; Inert atmosphere;
Stage #2: Dichlorophenylphosphine In tetrahydrofuran; hexane at -78 - 20℃; for 15h; Inert atmosphere;
100%
With R3N
With pyridine
dibenzylmercury(II)
780-24-5

dibenzylmercury(II)

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

benzyl-phenylchlorophosphine
29949-68-6, 73365-16-9

benzyl-phenylchlorophosphine

Conditions
ConditionsYield
at 60℃; for 24h;100%
LiCH2PMe2
64065-06-1

LiCH2PMe2

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

(Bis-dimethylphosphanylmethyl-phosphanyl)-benzene

(Bis-dimethylphosphanylmethyl-phosphanyl)-benzene

Conditions
ConditionsYield
In tetrahydrofuran -78 deg C; RT, 12 h;100%
3-methoxyphenyl bromide
2398-37-0

3-methoxyphenyl bromide

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

bis(3-methoxyphenyl)(phenyl)phosphine oxide
216164-54-4

bis(3-methoxyphenyl)(phenyl)phosphine oxide

Conditions
ConditionsYield
Stage #1: 3-methoxyphenyl bromide With magnesium Metallation;
Stage #2: Dichlorophenylphosphine Arylation;
Stage #3: With water; dihydrogen peroxide In tetrahydrofuran Oxidation; Further stages.;
100%
With magnesium Yield given;
2-(2'-Hydroxyphenyl)benzimidazole
2963-66-8

2-(2'-Hydroxyphenyl)benzimidazole

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

3,4-benzimidazole-5,6-benzo-2-phenyl-1,3,2-oxazaphosphorinane
769124-06-3

3,4-benzimidazole-5,6-benzo-2-phenyl-1,3,2-oxazaphosphorinane

Conditions
ConditionsYield
With triethylamine In toluene at 20℃;100%
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

cyanomethyl bromide
590-17-0

cyanomethyl bromide

bis(cyanomethyl)phenylphosphine
61806-56-2

bis(cyanomethyl)phenylphosphine

Conditions
ConditionsYield
With iodine; zinc In tetrahydrofuran for 1h; Heating;100%
pentafluoroethanesulfonyl azide

pentafluoroethanesulfonyl azide

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

CF3SO2NPCl2C6H5
30227-07-7

CF3SO2NPCl2C6H5

Conditions
ConditionsYield
100%
dilithium 1,2-dicarba-closo-dodecaborane(12)-1,2-diselenolate

dilithium 1,2-dicarba-closo-dodecaborane(12)-1,2-diselenolate

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

2-phenyl-4,5-[1,2(1,2-dicarba-closo-dodecaborano)]-1,3-diselena-2-phospha-cyclopentane
1017605-86-5

2-phenyl-4,5-[1,2(1,2-dicarba-closo-dodecaborano)]-1,3-diselena-2-phospha-cyclopentane

Conditions
ConditionsYield
In diethyl ether C6H5PCl2 added at -78°C to Se-compound in ether; stirred overnight at room temp.; filtered off; concd.; crystallized from CH2Cl2 at room temp.;100%
C46H60O10
1224196-01-3

C46H60O10

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

C70H72O14P4
1224196-04-6

C70H72O14P4

Conditions
ConditionsYield
Stage #1: C46H60O10; Dichlorophenylphosphine With pyridine at 20 - 70℃;
Stage #2: With dihydrogen peroxide In chloroform; water at 20℃; for 0.5h;
100%
3-bromo-2-(2-bromophenyl)benzo[b]thiophene
1263143-03-8

3-bromo-2-(2-bromophenyl)benzo[b]thiophene

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

10-phenyl-10H-benzo[b]phosphindolo[2,3-d]thiophene
1263143-04-9

10-phenyl-10H-benzo[b]phosphindolo[2,3-d]thiophene

Conditions
ConditionsYield
Stage #1: 3-bromo-2-(2-bromophenyl)benzo[b]thiophene With n-butyllithium In diethyl ether; hexane at -78 - 20℃; for 2h; Inert atmosphere;
Stage #2: Dichlorophenylphosphine In diethyl ether; hexane at 20℃; for 3h; Inert atmosphere;
100%
Stage #1: 3-bromo-2-(2-bromophenyl)benzo[b]thiophene With n-butyllithium; N,N,N,N,-tetramethylethylenediamine In diethyl ether at -78℃; for 1h; Inert atmosphere;
Stage #2: Dichlorophenylphosphine In diethyl ether at -78 - 20℃; Inert atmosphere;
70%
Stage #1: 3-bromo-2-(2-bromophenyl)benzo[b]thiophene With n-butyllithium In diethyl ether; hexane at -20℃; for 0.25h; Inert atmosphere;
Stage #2: Dichlorophenylphosphine In diethyl ether; hexane at -20 - 20℃; for 15h; Inert atmosphere;
68%
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

2,2-difluoro-1,3-dimethyl-imidazolidine
220405-40-3

2,2-difluoro-1,3-dimethyl-imidazolidine

C11H15F4N2P
1352439-95-2

C11H15F4N2P

Conditions
ConditionsYield
In diethyl ether at -40℃; for 12h; Inert atmosphere;100%
C5H10Cl4N2Si
1421683-29-5

C5H10Cl4N2Si

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

C11H15Cl2N2P
1421683-31-9

C11H15Cl2N2P

Conditions
ConditionsYield
In tetrahydrofuran at 0 - 20℃; for 12h;100%
(2-fluorophenyl)2PN(i-propyl)H
1065189-00-5

(2-fluorophenyl)2PN(i-propyl)H

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

C21H20ClF2NP2
1448244-21-0

C21H20ClF2NP2

Conditions
ConditionsYield
Stage #1: (2-fluorophenyl)2PN(i-propyl)H With n-butyllithium In pentane at -78℃; for 1h; Inert atmosphere;
Stage #2: Dichlorophenylphosphine In pentane at -70℃; for 1.5h; Inert atmosphere;
100%
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

diphenyl(trimethylsilylmethyl)phosphane
4451-96-1

diphenyl(trimethylsilylmethyl)phosphane

C19H17ClP2

C19H17ClP2

Conditions
ConditionsYield
at 95℃; for 1h; Inert atmosphere;100%
at 95℃; for 1h; Inert atmosphere;100%
2-((trimethylsilyl)methyl)quinoline
65094-35-1

2-((trimethylsilyl)methyl)quinoline

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

phenylbis(quinolin-2-ylmethyl)phosphine

phenylbis(quinolin-2-ylmethyl)phosphine

Conditions
ConditionsYield
In tetrahydrofuran for 18h; Cooling;100%
In tetrahydrofuran at 0℃;
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

isoprene
78-79-5

isoprene

3-Methyl-1-phenyl-2-phospholene 1-oxide
707-61-9

3-Methyl-1-phenyl-2-phospholene 1-oxide

Conditions
ConditionsYield
With 2,6-di-tert-butyl-4-methyl-phenol In chloroform at 65℃; for 24h; Inert atmosphere; Sealed tube; Large scale;99.1%
McCormack reaction;68%
With 2,6-di-tert-butyl-4-methyl-phenol In toluene at 59 - 86℃; for 24h; Temperature; Inert atmosphere;5.204 g
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

dimethyl amine
124-40-3

dimethyl amine

bis(dimethylamino)phenyl phosphine
6143-71-1

bis(dimethylamino)phenyl phosphine

Conditions
ConditionsYield
In diethyl ether at 0℃; for 2h;99%
In Petroleum ether for 0.5h; Ambient temperature;83%
In diethyl ether at 5℃; for 3h;82%
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

[Sn(CH3)2(1,2-benzenedithiolate)]
153260-18-5

[Sn(CH3)2(1,2-benzenedithiolate)]

2-Phenyl-benzo[1,3,2]dithiaphosphole

2-Phenyl-benzo[1,3,2]dithiaphosphole

Conditions
ConditionsYield
In benzene for 0.25h; Ambient temperature;99%
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

4,7-diisopropyl-2,2-dimethyl-1,3,2-benzodithiastannole
157768-68-8

4,7-diisopropyl-2,2-dimethyl-1,3,2-benzodithiastannole

4,7-Diisopropyl-2-phenyl-benzo[1,3,2]dithiaphosphole

4,7-Diisopropyl-2-phenyl-benzo[1,3,2]dithiaphosphole

Conditions
ConditionsYield
In benzene for 0.25h; Ambient temperature;99%
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

4,7-diisopropyl-2,2-dimethyl-1,3,2-benzodiselenastannole

4,7-diisopropyl-2,2-dimethyl-1,3,2-benzodiselenastannole

4,7-Diisopropyl-2-phenyl-benzo[1,3,2]diaselenaphosphole

4,7-Diisopropyl-2-phenyl-benzo[1,3,2]diaselenaphosphole

Conditions
ConditionsYield
In benzene for 0.25h; Ambient temperature;99%
thiobenzoic acid potassium salt
28170-13-0

thiobenzoic acid potassium salt

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

A

bis(benzoylthio)phenylphosphine

bis(benzoylthio)phenylphosphine

B

KCl

KCl

Conditions
ConditionsYield
In dichloromethane at 20℃; for 1h; Substitution;A 99%
B n/a
potassium 4-methoxybenzenecarbothioate
7429-03-0

potassium 4-methoxybenzenecarbothioate

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

A

bis(4-methoxybenzoylthio)phenylphosphine

bis(4-methoxybenzoylthio)phenylphosphine

B

KCl

KCl

Conditions
ConditionsYield
In dichloromethane at 20℃; for 1h; Substitution;A 99%
B n/a
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

(S)-N,N'-bis(methylsulfonyl)-1,1'-binaphthyl-2,2'-diamine

(S)-N,N'-bis(methylsulfonyl)-1,1'-binaphthyl-2,2'-diamine

3,5-bis-methanesulfonyl-4-phenyl-4,5-dihydro-3H-3,5-diaza-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalene

3,5-bis-methanesulfonyl-4-phenyl-4,5-dihydro-3H-3,5-diaza-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalene

Conditions
ConditionsYield
With n-butyllithium In tetrahydrofuran; hexane at -78 - 20℃;99%
Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

woollins’ reagent
122039-27-4

woollins’ reagent

Conditions
ConditionsYield
With selenium; ammonia; sodium In toluene at -78℃; for 68h; Inert atmosphere; Schlenk technique; Reflux;99%
Stage #1: Dichlorophenylphosphine With sodium selenide In toluene for 64h; Heating;
Stage #2: With selenium In toluene for 3.5h; Heating;
82%
arachno-6-SB9H11

arachno-6-SB9H11

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

nido-10-Ph-7,10-SPB9H9
214554-58-2

nido-10-Ph-7,10-SPB9H9

Conditions
ConditionsYield
With 1,8-bis(dimethylamino)naphthalene; HCl In 1,2-dimethoxyethane byproducts: (proton sponge)H(+)Cl(-); N2-atmosphere; addn. of proton sponge and then phosphine to borane, standing for 16 h; filtration, evapn. (vac.), extn. into Et2O, HCl addn., filtration, evapn., drying (vac.); elem. anal.;99%
[(η5-C5H5)(η5,η1,η1-C5H4CMe2(CH2)2CHCH2C6H4)Zr]

[(η5-C5H5)(η5,η1,η1-C5H4CMe2(CH2)2CHCH2C6H4)Zr]

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

[(η5-C5H5)(η5-C5H4CMe2(CH2)2C8H7PPh)ZrCl2]
1312761-78-6

[(η5-C5H5)(η5-C5H4CMe2(CH2)2C8H7PPh)ZrCl2]

Conditions
ConditionsYield
In (2)H8-toluene Ar; ligand added dropwise to toluene-d8 soln. of Zr compd. (1:1 molar ratio), mixt. stirred for 30 min; NMR;99%
1,8-dibromonaphthalene
17135-74-9

1,8-dibromonaphthalene

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

C26H17Br2OP

C26H17Br2OP

Conditions
ConditionsYield
Stage #1: 1,8-dibromonaphthalene With n-butyllithium In diethyl ether at -80 - 20℃; for 1h; Inert atmosphere; Schlenk technique;
Stage #2: Dichlorophenylphosphine In diethyl ether at -80 - 20℃; Inert atmosphere; Schlenk technique;
Stage #3: With dihydrogen peroxide In dichloromethane for 2h; Inert atmosphere; Schlenk technique;
99%
2,2':6,2''-terpyridine
1148-79-4

2,2':6,2''-terpyridine

sodium tetrakis(pentafluorophenyl)-borate
2797-28-6

sodium tetrakis(pentafluorophenyl)-borate

Dichlorophenylphosphine
644-97-3

Dichlorophenylphosphine

2C24BF20(1-)*C21H16N3P(2+)

2C24BF20(1-)*C21H16N3P(2+)

Conditions
ConditionsYield
In dichloromethane Inert atmosphere;98.8%

644-97-3Relevant articles and documents

-

Dye

, p. 2595 (1948)

-

AlCl3-catalyzed C-H p hosphination of benzene: A mechanistic study

Duan, Haodong,Gao, Jun,Guo, Ge,Han, Yuxi,Leng, Kangwei,Li, Xinjin,Wang, Zhongwei,Xu, Xiaolei,Yu, Qing

, (2021/01/06)

The characteristics of the reaction for the preparation of dichlorophenylphosphine (DCPP) via benzene and PCl3 in the presence of AlCl3 were studied. Some unique characteristics were observed when a catalytic amount of AlCl3 was used. Namely, more than one mole of DCPP was obtained per mole AlCl3, the reaction solution was layered, and DCPP could be directly separated. Our mechanistic study showed that benzene reacted with PCl3 to form DCPP-AlCl3, and DCPP-AlCl3 dissociated into DCPP and AlCl3, continuing to catalyze this reaction. This resulted in the high catalytic efficiency of AlCl3. The layering of the reaction solution was caused by the immiscibility of DCPP-AlCl3 with the raw materials, greatly facilitating the dissociation process of DCPP-AlCl3. The formation of diphenylphosphorus chloride (DPC) was due to a continuous Friedel-Crafts reaction between DCPP and benzene. DPC cooperated with AlCl3 to form the stable coordination compound DPC-AlCl3 that did not dissociate and was responsible for the deactivation of AlCl3.

Ionic liquid modified silica gel loaded aluminum chloride catalyst (by machine translation)

-

Paragraph 0034-0047, (2020/10/04)

The ionic liquid modified silica gel loaded aluminum chloride catalyst is prepared by mixing and stirring ionic liquid and silica gel, heating to, stirring the ionic liquid modified silica gel obtained in step a, stirring 100 - 150 °C under stirring, removing 1 - 2h ethanol under stirring, heating the mixture under reduced pressure to, and carrying out reaction to obtain yellow powder b 5 - 10h 120 - 160 °C 1 - 2hIn the process of preparing the phenyldiphosphine chloride, very high yield (above 90%) can be achieved, the catalyst removal system is simple in post-treatment, and the catalyst can be removed only through filtration, and the catalyst can be reused after being dried. (by machine translation)

Semiconducting Material Comprising a Phosphine Oxide Matrix and Metal Salt

-

, (2018/05/03)

The present invention is directed to a semiconducting material comprising: i) a compound according to formula (I) wherein R1, R2 and R3 are independently selected from C1-C30-alkyl, C3-C30 cycloalkyl, C2-C30-heteroalkyl, C6-C30-aryl, C2-C30-heteroaryl, C1-C30-alkoxy, C3-C30-cycloalkyloxy, C6-C30 aryloxy, and from structural unit having general formula E-A-, wherein—A is a C6-C30 phenylene spacer unit, and—E is an electron transporting unit that is selected from C10-C60 aryl and C6-C60 heteroaryl comprising up to 6 heteroatoms independently selected from O, S, P, Si and B and that comprises a conjugated system of at least 10 delocalized electrons, and—at least one group selected from R1, R2 and R3 has the general formula E-A-; and ii) at least one complex of a monovalent metal having formula (II) wherein—M+ is a positive metal ion bearing a single elementary charge, and each of A1, A2, A3 and A4 is independently selected from H, substituted or unsubstituted C6-C20 aryl and substituted or unsubstituted C2-C20 heteroaryl, wherein a heteroaryl ring of at least 5 ring-forming atoms of the substituted or unsubstituted C2-C20 heteroaryl comprises at least one hetero atom selected from O, S and N.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 644-97-3