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1558-25-4

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1558-25-4 Usage

Chemical Properties

Different sources of media describe the Chemical Properties of 1558-25-4 differently. You can refer to the following data:
1. Colorless clear liquid
2. Trichloro(chloromethyl)silane is a colorless liquid. Sharp, biting odor.

Uses

(chloromethyl)trichlorosilane is usede in the synthesis of a highly branched polycarbosilane. Ferrocenophane has been prepared from (chloromethyl)trichlorosilane.

General Description

Liquid.

Air & Water Reactions

Highly flammable. Reacts vigorously with water to form hydrogen chloride (hydrochloric acid)

Reactivity Profile

Chlorosilanes, such as (Chloromethyl)trichlorosilane, are compounds in which silicon is bonded to from one to four chlorine atoms with other bonds to hydrogen and/or alkyl groups. Chlorosilanes react with water, moist air, or steam to produce heat and toxic, corrosive fumes of hydrogen chloride. They may also produce flammable gaseous H2. They can serve as chlorination agents. Chlorosilanes react vigorously with both organic and inorganic acids and with bases to generate toxic or flammable gases.

Health Hazard

(Non-Specific -- Methyl Trichlorosilane) If inhaled, may be harmful; contact may cause burns to skin and eyes. Runoff from fire control or dilution water may cause pollution.

Fire Hazard

(Non-specific -- Methyl Trichloro- silane) Flammable/Combustible material; may be ignited by heat, sparks, or flames. Vapors may travel to a source of ignition and flash back. Container may explode in heat of fire. Vapor explosion hazard indoors, outdoors, or in sewers. Runoff to sewer may create fire or explosion hazard. May react violently with water.

Potential Exposure

Used in the synthesis of polysiloxane (silicone polymers).

Shipping

UN3389 Toxic by inhalation liquid, corrosive, n.o.s. with an LC50 ≤200 mL/m3 and saturated vapor concentration ≥500 Hazard Class: 6.1; Labels: 6.1-Poisonous materials, 8-Corrosive material, Technical Name Required, Inhalation Hazard Zone A. UN1295 Trichlorosilane, Hazard Class: 4.3; Labels: 4.3-Dangerous when wet material, 3-Flammable liquid, 8-Corrosive material.

Incompatibilities

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Chlorosilanes react vigorously with bases and both organic and inorganic acids generating toxic and/or flammable gases. Chlorosilanes react with water, moist air, or steam to produce heat and toxic, corrosive fumes of hydrogen chloride. They may also produce flammable gaseous hydrogen. Attacks metals in the presence of moisture.

Check Digit Verification of cas no

The CAS Registry Mumber 1558-25-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,5 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1558-25:
(6*1)+(5*5)+(4*5)+(3*8)+(2*2)+(1*5)=84
84 % 10 = 4
So 1558-25-4 is a valid CAS Registry Number.
InChI:InChI=1/CH2Cl4Si/c2-1-6(3,4)5/h1H2

1558-25-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (L16433)  (Chloromethyl)trichlorosilane, 97%   

  • 1558-25-4

  • 5g

  • 178.0CNY

  • Detail
  • Alfa Aesar

  • (L16433)  (Chloromethyl)trichlorosilane, 97%   

  • 1558-25-4

  • 25g

  • 786.0CNY

  • Detail

1558-25-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (Chloromethyl)trichlorosilane

1.2 Other means of identification

Product number -
Other names trichloro(chloromethyl)silane

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:1558-25-4 SDS

1558-25-4Synthetic route

Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

Conditions
ConditionsYield
With chlorine Irradiation;98%
With chlorine at 65℃; for 6.5h; Irradiation; visible light;68%
With chlorine im UV-Licht;
trichloromethyltrichlorosilane
17760-13-3

trichloromethyltrichlorosilane

methyldiphenylsilane
776-76-1

methyldiphenylsilane

A

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

B

trichloro(dichloromethyl)silane
1558-24-3

trichloro(dichloromethyl)silane

C

chloromethyldiphenylsilane
144-79-6

chloromethyldiphenylsilane

Conditions
ConditionsYield
at 160 - 240℃; for 6h;A 12.3%
B 85.3%
C 97.5%
trichloro(dichloromethyl)silane
1558-24-3

trichloro(dichloromethyl)silane

methyldiphenylsilane
776-76-1

methyldiphenylsilane

A

Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

B

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

C

chloromethyldiphenylsilane
144-79-6

chloromethyldiphenylsilane

Conditions
ConditionsYield
at 160 - 240℃; for 6h;A 15.6%
B 81.2%
C 93.1%
Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

A

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

B

trichloro(dichloromethyl)silane
1558-24-3

trichloro(dichloromethyl)silane

Conditions
ConditionsYield
With chlorine for 60h; Heating; Irradiation;A 87%
B 9%
With chlorine at 70 - 80℃; Photolysis;
Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

A

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

B

trichloro(dichloromethyl)silane
1558-24-3

trichloro(dichloromethyl)silane

C

trichloromethyltrichlorosilane
17760-13-3

trichloromethyltrichlorosilane

Conditions
ConditionsYield
With chlorine at 250℃; for 20h; Product distribution; Further Variations:; Temperatures; time;A 85.9%
B n/a
C n/a
With chlorine Irradiation;A 70%
B 5%
C 1%
Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

A

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

B

trichloro(dichloromethyl)silane
1558-24-3

trichloro(dichloromethyl)silane

C

Trichlorosilanyl-methanesulfonyl chloride
77428-12-7

Trichlorosilanyl-methanesulfonyl chloride

D

Chloro-trichlorosilanyl-methanesulfonyl chloride
77428-13-8

Chloro-trichlorosilanyl-methanesulfonyl chloride

Conditions
ConditionsYield
With yttrium(III) chloride; sulfuryl dichloride at 70℃; for 10h; Product distribution; Irradiation; other catalysts (HoCl3,TmCl3);A 20%
B 31%
C 1.5%
D 6.5%
With yttrium(III) chloride; sulfuryl dichloride at 50 - 70℃; Product distribution; Irradiation; various inorganic additives (chlorides and oxychlorides of 32 elements); effect of inorganic chlorides and oxychlorides on the photochemical reaction of methylchlorosilanes with SO2Cl2;A 22 % Spectr.
B 31 % Spectr.
C 1.5 % Spectr.
D 6.5 % Spectr.
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

Conditions
ConditionsYield
With tetrachlorosilane; diethyl ether; copper at -60℃;
With tetrachlorosilane; diethyl ether; copper at -78℃;
With tetrachlorosilane; diethyl ether at -50℃;
Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

A

methylene chloride
74-87-3

methylene chloride

B

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

C

trichloro(dichloromethyl)silane
1558-24-3

trichloro(dichloromethyl)silane

D

trichloromethyltrichlorosilane
17760-13-3

trichloromethyltrichlorosilane

Conditions
ConditionsYield
With chlorine at 80℃; for 17h; Further byproducts given;A 0.7 g
B 35.4 g
C 5 g
D 3.9 g
dichloromethane
75-09-2

dichloromethane

A

chloroform
67-66-3

chloroform

B

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

C

1,1,1,3,3,3-hexachloro-1,3-disilapropane
4142-85-2

1,1,1,3,3,3-hexachloro-1,3-disilapropane

Conditions
ConditionsYield
With hexachlorodisilane at 399℃; Product distribution; var. temp. and molar ratio;
trichloro(dichloromethyl)silane
1558-24-3

trichloro(dichloromethyl)silane

copper silicon-alloy

copper silicon-alloy

A

Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

B

tetrachlorosilane
10026-04-7, 53609-55-5

tetrachlorosilane

C

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

D

1,1,1,3,3,3-hexachloro-1,3-disilapropane
4142-85-2

1,1,1,3,3,3-hexachloro-1,3-disilapropane

Conditions
ConditionsYield
at 360℃;
tetrachlorosilane
10026-04-7, 53609-55-5

tetrachlorosilane

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

Conditions
ConditionsYield
In not given at low temp.;;
In diethyl ether byproducts: N2; SiCl4 and diazomethane in ether at about -50°C; vigorous react. under formation of N2;;45-47
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

ethylmagnesium chloride
2386-64-3

ethylmagnesium chloride

triethylchloromethylsilane
757-34-6

triethylchloromethylsilane

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; Inert atmosphere; Schlenk technique;98%
In tetrahydrofuran at 0 - 20℃;
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

isopropyl alcohol
67-63-0

isopropyl alcohol

(chloromethyl)triisopropoxysilane
18162-82-8

(chloromethyl)triisopropoxysilane

Conditions
ConditionsYield
With 1H-imidazole; dmap In dichloromethane at 0 - 20℃; for 12h; Inert atmosphere; Schlenk technique;97%
With triethylamine In hexane at 25 - 65℃; for 6h; Large scale;78%
at 120℃;
triisopropanolamine
122-20-3

triisopropanolamine

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

1-chloromethyl-3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecane
57078-94-1, 64235-15-0, 64235-26-3

1-chloromethyl-3,7,10-trimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecane

Conditions
ConditionsYield
In chloroform97%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

1,3-bis(trimethylsilyl)tetrahydropyrimidin-2-one
18132-77-9

1,3-bis(trimethylsilyl)tetrahydropyrimidin-2-one

1,3-bis[(trichlorosilyl)methyl]tetrahydropyrimidin-2-one
884865-46-7

1,3-bis[(trichlorosilyl)methyl]tetrahydropyrimidin-2-one

Conditions
ConditionsYield
In hexane for 27h; Inert atmosphere; Schlenk technique;96%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

HSiPh3
789-25-3

HSiPh3

A

Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

B

Triphenylsilyl chloride
76-86-8

Triphenylsilyl chloride

Conditions
ConditionsYield
at 165 - 250℃; for 12h;A 87.3%
B 95.8%
at 165 - 210℃; for 12h;A 95.8%
B 87.3%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

methyldiphenylsilane
776-76-1

methyldiphenylsilane

A

Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

B

chloromethyldiphenylsilane
144-79-6

chloromethyldiphenylsilane

Conditions
ConditionsYield
at 125 - 210℃; for 12h;A 90.2%
B 95.6%
at 125 - 210℃; for 12h;A 95.6%
B 90.2%
ethyl methyl ketone oxime
96-29-7

ethyl methyl ketone oxime

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

chloromethyltris(methylethylketoxime)silane

chloromethyltris(methylethylketoxime)silane

Conditions
ConditionsYield
In hexane at 20℃; for 3h; Inert atmosphere;95%
In Petroleum ether at 25℃; for 4h; Solvent; Temperature;
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

1,3,4,6,7,8-hexahydro-1-trimethylsilyl-2H-pyrimido<1,2-a>pyrimidin
149758-20-3

1,3,4,6,7,8-hexahydro-1-trimethylsilyl-2H-pyrimido<1,2-a>pyrimidin

Trichloro-(3,4,7,8-tetrahydro-2H,6H-pyrimido<1,2-a>pyrimidin-1-ylmethyl-C1,N9)-silicium

Trichloro-(3,4,7,8-tetrahydro-2H,6H-pyrimido<1,2-a>pyrimidin-1-ylmethyl-C1,N9)-silicium

Conditions
ConditionsYield
at 25℃;93.5%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

1,3,4,6,7,8-hexahydro-1-methyl-2H-pyrimido[1,2-a]pyrimidine

1,3,4,6,7,8-hexahydro-1-methyl-2H-pyrimido[1,2-a]pyrimidine

Trichloro-(3,4,7,8-tetrahydro-2H,6H-pyrimido<1,2-a>pyrimidin-1-ylmethyl-C1,N9)-silicium

Trichloro-(3,4,7,8-tetrahydro-2H,6H-pyrimido<1,2-a>pyrimidin-1-ylmethyl-C1,N9)-silicium

Conditions
ConditionsYield
In benzene at 25℃;92%
2-(trimethylsilyloxy)pyridine
18292-04-1

2-(trimethylsilyloxy)pyridine

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

1-trichlorosilylmethylpyrid-2-one
138169-76-3

1-trichlorosilylmethylpyrid-2-one

Conditions
ConditionsYield
In hexane Alkylation; desilylation, rearrangement;92%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

Dimethylphenylsilane
766-77-8

Dimethylphenylsilane

A

Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

B

phenyldimethylsilyl chloride
768-33-2

phenyldimethylsilyl chloride

Conditions
ConditionsYield
at 125 - 210℃; for 2h;A 91.4%
B 88.6%
trimethylsilan
993-07-7

trimethylsilan

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

A

chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

B

Methyltrichlorosilane
75-79-6

Methyltrichlorosilane

Conditions
ConditionsYield
at 500℃; for 0.00833333h;A 86.8%
B 91.2%
at 500℃; for 0.00833333h;A 91.2%
B 86.8%
ethanol
64-17-5

ethanol

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

chloromethyltriethoxysilane
15267-95-5

chloromethyltriethoxysilane

Conditions
ConditionsYield
In hexane at -20℃; Inert atmosphere; Schlenk technique;91%
With tin(IV) chloride; cyclohexene for 1h; Ambient temperature;75.1%
With urea In Petroleum ether at 65℃; for 5h; Inert atmosphere;60%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

N,N-bis(2-hydroxypropyl)-N-(hydroxyethyl)amine
10353-86-3

N,N-bis(2-hydroxypropyl)-N-(hydroxyethyl)amine

1-chloromethyl-3,7-dimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecane
57078-93-0

1-chloromethyl-3,7-dimethyl-2,8,9-trioxa-5-aza-1-sila-bicyclo[3.3.3]undecane

Conditions
ConditionsYield
In chloroform91%
6-methyl-2-trimethylsiloxypyridine
61553-19-3

6-methyl-2-trimethylsiloxypyridine

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

1-trichlorosilylmethyl-6-methylpyrid-2-one

1-trichlorosilylmethyl-6-methylpyrid-2-one

Conditions
ConditionsYield
In hexane Alkylation; desilylation, rearrangement;91%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

2,2',2''-tris(trimethylsiloxy)triethylamine
20836-42-4

2,2',2''-tris(trimethylsiloxy)triethylamine

A

1-(chloromethyl)silatrane
42003-39-4

1-(chloromethyl)silatrane

B

chloro-trimethyl-silane
75-77-4

chloro-trimethyl-silane

Conditions
ConditionsYield
at 140 - 150℃; Yields of byproduct given;A 90%
B n/a
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

6-chloro-2-trimethylsiloxypyridine
252980-63-5

6-chloro-2-trimethylsiloxypyridine

1-trichlorosilylmethyl-6-chloropyrid-2-one

1-trichlorosilylmethyl-6-chloropyrid-2-one

Conditions
ConditionsYield
In hexane Alkylation; desilylation, rearrangement;90%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

phenylmagnesium bromide

phenylmagnesium bromide

phenyl(chloromethyl)dichlorosilane
5489-23-6

phenyl(chloromethyl)dichlorosilane

Conditions
ConditionsYield
In diethyl ether at 25℃;89%
1-[N,N-bis(2-hydroxyethyl)amino]-2-propanol
6712-98-7

1-[N,N-bis(2-hydroxyethyl)amino]-2-propanol

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

1-(chloromethyl)-3-methylsilatrane
57593-16-5

1-(chloromethyl)-3-methylsilatrane

Conditions
ConditionsYield
In chloroform88%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

O-trimethylsilyl-N-(triphenylphosphinimino)-4-(t-butyl)benzohydrazide

O-trimethylsilyl-N-(triphenylphosphinimino)-4-(t-butyl)benzohydrazide

bis[N-(triphenylphosphinimino)-4-t-butyl-phenyl-N',O](chloromethyl)siliconium chloride

bis[N-(triphenylphosphinimino)-4-t-butyl-phenyl-N',O](chloromethyl)siliconium chloride

Conditions
ConditionsYield
In chloroform at 20℃; for 0.5h; Inert atmosphere; Schlenk technique;88%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

1,1,3,3-tetraphenyldisiloxane-1,3-diol
1104-93-4

1,1,3,3-tetraphenyldisiloxane-1,3-diol

A

2-Chloro-2-chloromethyl-4,4,6,6-tetraphenyl-[1,3,5,2,4,6]trioxatrisilinane
79891-82-0

2-Chloro-2-chloromethyl-4,4,6,6-tetraphenyl-[1,3,5,2,4,6]trioxatrisilinane

B

C26H24Cl6O3Si4

C26H24Cl6O3Si4

Conditions
ConditionsYield
With pyridine In toluene for 3h; Heating;A n/a
B 87.6%
bis(triethylgermyl)mercury
4149-28-4

bis(triethylgermyl)mercury

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

(Cl3SiCH2)2Hg
86808-03-9

(Cl3SiCH2)2Hg

Conditions
ConditionsYield
In benzene byproducts: Et3GeCl; Irradiation (UV/VIS); in sealed ampul; irradiated for 15 min (distance of 10 cm); distild. (vac.); elem.anal.;87.1%
In benzene byproducts: Et3GeCl; Irradiation (UV/VIS); Ge-compd. addn. to Si-compd. soln., sealing in evac. ampul, irradiation (DRT-375 quartz mercury lamp) until orange color of Ge-compd. disappeared (3 min); fractionation; elem. anal.;87.1%
methanol
67-56-1

methanol

(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

(chloromethyl)trimethoxysilane
5926-26-1

(chloromethyl)trimethoxysilane

Conditions
ConditionsYield
With urea In diethyl ether for 4h; Reflux; Inert atmosphere;87%
In Petroleum ether for 2h; Ambient temperature;83%
In hexane at -20℃; Inert atmosphere; Schlenk technique;81%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

phenol
108-95-2

phenol

chloromethyltriphenoxysilane

chloromethyltriphenoxysilane

Conditions
ConditionsYield
for 8h; Heating;86%
(chloromethyl)trichlorosilane
1558-25-4

(chloromethyl)trichlorosilane

<(trimethylsilyl)thio>pyridine
112247-55-9

<(trimethylsilyl)thio>pyridine

1-(trichlorosilylmethylmercapto)pyridine

1-(trichlorosilylmethylmercapto)pyridine

Conditions
ConditionsYield
In benzene for 0.333333h; Alkylation; desilylation;86%

1558-25-4Relevant articles and documents

-

Seyferth,Rochow

, (1960)

-

NOVEL ECO-FRIENDLY INSECTICIDES BASED ON SILICON COMPOUNDS AND PROCESS OF PREPARATION THEREOF

-

Page/Page column 13, (2018/08/26)

The present invention provides novel silicon-based compounds or salt thereof of general formula (I), wherein R1 and R2 Represent the Halogen, Hydrogen, alkyl, alkoxy or aryl group and R3, R4, R5 and R6 represents Chlorine or Hydrogen or hydroxyl group. The said compounds are biodegradable active insecticides. The invention also relates to process for the manufacture of said compounds and compositions containing them and their use.

REACTION OF HEXACHLORODISILANE WITH METHYLENE DICHLORIDE

Chernyshev, E. A.,Komalenkova, N. G.,Bykovchenko, V. G.,Kapitova, I. A.

, p. 383 - 386 (2007/10/03)

Reaction of hexachlorodisilane with methylene dichloride at 400-520 deg C involves two consecutive-parallel reactions yielding chloromethyltrichlorosilane and bis(trichlorosilyl)methane.The ratios of the rate constants of these reactions and the maximal yield of the intermediate chloromethyltrichlorosilane have been determined at various temperatures.Side reactions that yield tris(trichlorosilyl)methane have been examined.

SELECTIVE LASER-INDUCED PHOTOCHEMICAL CHLORINATION OF METHYLTRICHLOROGERMANE AND METHYLTRICHLOROSILANE

Zueva, G. Ya.,Khaustova, T. I.,Serezhkina, N. V.,El'tsov, K. N.

, p. 1316 (2007/10/02)

-

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