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1558-24-3

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1558-24-3 Usage

Chemical Properties

Colorless clear liquid

Uses

Trichloro(dichloromethyl)silane is a useful reagent for organic synthesis. It is used in the synthesis of silylated ethenes, acetylenes and other organosilicon compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1558-24-3 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 1558-24:
(6*1)+(5*5)+(4*5)+(3*8)+(2*2)+(1*4)=83
83 % 10 = 3
So 1558-24-3 is a valid CAS Registry Number.
InChI:InChI=1/CHCl5Si/c2-1(3)7(4,5)6/h1H

1558-24-3 Well-known Company Product Price

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  • Aldrich

  • (479039)  Trichloro(dichloromethyl)silane  96%

  • 1558-24-3

  • 479039-25ML

  • 3,465.54CNY

  • Detail

1558-24-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trichloro(dichloromethyl)silane

1.2 Other means of identification

Product number -
Other names trichloro-dichloromethyl-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:1558-24-3 SDS

1558-24-3Relevant articles and documents

CHLORINATION OF METHYLTRICHLOROSILANE IN A BARRIER DISCHARGE

Voronkov, M. G.,Stankevich, V. K.,Kukharev, B. F.,Artemov, I. P.

, p. 1697 - 1698 (1986)

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SELECTIVE LASER-INDUCED PHOTOCHEMICAL CHLORINATION OF METHYLTRICHLOROGERMANE AND METHYLTRICHLOROSILANE

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

, p. 1316 (1986)

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Si-C coupling reaction of polychloromethanes with HSiCl3 in the presence of Bu4PCl: Convenient synthetic method for bis(chlorosilyl)methanes

Jung, Dong Euy,Kang, Seung-Hyun,Han, Joon Soo,Lim, Weon Cheol,Park, Young-ae W.,Yoo, Bok Ryul

, p. 3901 - 3906 (2008/03/12)

Coupling reaction of polychloromethanes CH4-nCln (n = 2-4) with HSiCl3 in the presence of tetrabutylphosphonium chloride (Bu4PCl) as a catalyst occurred at temperatures ranging from 30 °C to 150 °C. The reactivity of polychloromethanes increases as the number of chlorine-substituents on the carbon increases. In the reactions of CCl4 with HSiCl3, a variety of coupling products such as bis(chlorosilyl)methanes CH2(SiCl3)(SiXCl2) [X = Cl (1a), H (1b)], (chlorosilyl)trichloromthanes Cl3CSiXCl2 [X = Cl (2a), H (2b)], and (chlorosilyl)dichloromthanes Cl2HCSiXCl2 [X = Cl (3a), H (3b)] were obtained along with reductive dechlorination products such as CHCl3 and CH2Cl2 depending on the reaction temperature. In the reaction of CCl4, 2a is formed at the initial stage of the coupling reaction and converted to give CHCl3 at low temperature of 30 °C, to give 1a, 3a, and CHCl3 at 60 °C, and to afford 1a as major product and CH2Cl2 in competition above 100 °C. Si-H bond containing silylmethanes can be formed by the H-Cl exchange reaction with HSiCl3. Reaction of CHCl3 with HSiCl3 took placed at 80 °C to give three compounds 1a, 3a, and CH2Cl2, and finally 3a was converted to give 1a and CH2Cl2 at longer reaction time. While the condition for the reaction of CH2Cl2 with HSiCl3 required a much higher temperature of 150 °C. Under the optimized conditions for synthesizing bis(chlorosilyl)methanes 1a,b, a mixture of 1a and 1b were obtained as major products in 65% (1a:1b = 64:1) and 47% (42:5) yields from the reaction of CCl4 and CHCl3 at 100 °C for 8 h, respectively, and in 41% (34:7) yield from that of CH2Cl2 at 170 °C for 12 h. In the Si-C coupling reaction of polychloromethanes with HSiCl3, it seems likely that a trichlorosilyl anion generated from the reaction of HSiCl3 with Bu4PCl is an important key intermediate.

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