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6917-76-6

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6917-76-6 Usage

Uses

Chlorodimethylethylsilane, 97% is used in method of improving the hydrophobic properties of cellulosic materials without leaving an acidic residue.

Check Digit Verification of cas no

The CAS Registry Mumber 6917-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,1 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6917-76:
(6*6)+(5*9)+(4*1)+(3*7)+(2*7)+(1*6)=126
126 % 10 = 6
So 6917-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H11ClSi/c1-4-6(2,3)5/h4H2,1-3H3

6917-76-6 Well-known Company Product Price

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  • Alfa Aesar

  • (A13222)  Ethyldimethylchlorosilane, 97%   

  • 6917-76-6

  • 5g

  • 618.0CNY

  • Detail
  • Alfa Aesar

  • (A13222)  Ethyldimethylchlorosilane, 97%   

  • 6917-76-6

  • 25g

  • 2805.0CNY

  • Detail
  • Aldrich

  • (296473)  Chlorodimethylethylsilane  97%

  • 6917-76-6

  • 296473-5G

  • 472.68CNY

  • Detail

6917-76-6SDS

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 Chlorodimethylethylsilane

1.2 Other means of identification

Product number -
Other names Silane, chloroethyldimethyl-

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:6917-76-6 SDS

6917-76-6Relevant articles and documents

SELECTIVE PREPARATION OF VINYL- AND ETHYL-FUNCTIONALIZED CHLOROSILANES

-

Paragraph 0097-00107; 00108-00110, (2021/06/26)

A method of preparing an organosilicon compound via selective silylation of ethylene is disclosed. The method comprises reacting via silylation (A) a hydridochlorosilane compound and (B) ethylene in the presence of (C) a catalyst, thereby preparing the organosilicon compound. The silylation may be selectively conducted as a dehydrogenative coupling to prepare the organosilicon compound as a vinylchlorosilane compound, or as a hydrosilylation to prepare the organosilicon compound as an ethylchlorosilane compound. The catalyst (C) comprises a Ru(0) complex, and may be recycled for use in subsequent silylation reactions without purification. The organosilicon compound prepared according to the method is also disclosed.

Mechanistic studies on ethylene silylation with chlorosilanes catalysed by ruthenium complexes

Lachaize, Sebastien,Sabo-Etienne, Sylviane,Donnadieu, Bruno,Chaudret, Bruno

, p. 214 - 215 (2007/10/03)

Silylation of ethylene by chlorosilanes is catalysed by ruthenium complexes. Mechanistic investigations reveal the presence of a complicated network of reactions leading to new σ-silane, ethylene and silyl complexes.

Selectivite de la scission Si-C dans des composes du type Me3SiCH2Σ; une synthese originale et sure de l'iodoacetate d'ethyle

Bordeau, M.,Djamei, S. M.,Dunogues, J.

, p. 413 - 417 (2007/10/02)

The regiochemistry of the electrophilic cleavage of the SiCsp3 bond in compounds Me3SiCH2Σ (Σ = Me, Pr, Cl, COOEt) and Me3SiCHΣ2 (Σ = Cl) has been investigated using ICl, Me3SiOSO2Cl and HO3SCl as the electrophiles.When Σ = Pr or Cl a regioselective cleavage of the Si-CH3 bond was observed, producing silylated chlorosulfonates or sulfates which often were new compounds.With Σ = COOEt a regiospecific splitting of the Si-CH2COOEt bond was observed.This confirms the synthetic potential of ethyl trimethylsilylacetate.

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