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(TRICHLOROMETHYL)TRIMETHYLSILANE, also known as chlorotrimethylsilyl chloride or hexachloroethane, is a colorless, volatile, and highly reactive liquid with the chemical formula C3H6Cl6Si. It is an organosilicon compound that is widely used in the synthesis of various organosilicon compounds, particularly as a silylating agent in organic chemistry. (TRICHLOROMETHYL)TRIMETHYLSILANE is characterized by its strong reactivity with nucleophiles, making it a valuable tool in the formation of silyl ethers and other organosilicon derivatives. It is also used in the production of silicones and as a reagent in the pharmaceutical and chemical industries. Due to its high reactivity and potential hazards, it is essential to handle (TRICHLOROMETHYL)TRIMETHYLSILANE with extreme care, following proper safety protocols and guidelines.

5936-98-1

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5936-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5936-98-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 6 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5936-98:
(6*5)+(5*9)+(4*3)+(3*6)+(2*9)+(1*8)=131
131 % 10 = 1
So 5936-98-1 is a valid CAS Registry Number.

5936-98-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(trichloromethyl)silane

1.2 Other means of identification

Product number -
Other names Ruppert-Prakash reagent

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:5936-98-1 SDS

5936-98-1Relevant academic research and scientific papers

POLYMETHYLATION OF ORGANOCHLOROSILANES

Podol'skii, A. V.,Khonina, T. G.,Lyampasova, T. P.,Kodess, M. I.

, p. 1476 - 1480 (2007/10/03)

Polychloromethylation of Me3SiCl, Me2PhSiCl, Me2SiCl2, and MePhSiCl2 in the system magnesium-chloroform-THF has been studies under mild conditions (in the temperature renge 60 -65 deg C), and a scheme of formation of the main and by-products has been proposed.

Use of Sacrificial Anodes in Electrochemical Functionalization of Organic Halides

Chaussard, Jacques,Folest, Jean-Claude,Nedelec, Jean-Yves,Perichon, Jacques,Sibille, Soline,Troupel, Michel

, p. 369 - 381 (2007/10/02)

This article reviews the new possibilities in organic synthesis offered by the electroreduction of organic halides in the presence of various electrophiles using sacrificial metallic anodes.

Electrosynthese en chimie organosilicique: silylation selective de polychloromethanes

Pons, P.,Biran, C.,Bordeau, M.,Dunogues, J.

, p. 31 - 38 (2007/10/02)

Silylation by electroreduction of carbon tetrachloride, chloroform or methylene chloride is more selective than the common organometallic route.Me3SiCCl3 (94percent) and (Me3Si)2Cl2 (68percent) were thus obtained from CCl4, Me3SiCHCl2, (94percent) and (Me3Si)2CHCl (56percent) from CHCl3 and Me3SiCH2Cl (90percent) from CH2Cl2.Complete silylation of polychloromethanes was also successful by electrosynthesis and gave satisfactory yields.

EINTOPFSYNTHESE TRICHLOROMETHYLSUBSTITUIERTER ALKOHOLE

Brunner, Henri,Wimmer, Peter

, p. C4 - C6 (2007/10/02)

A new one-pot synthesis of alcohols RCH(OH)CCl3 starting from CCl4, Me3SiCl, Mg and aldehydes RCHO is described.

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