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5573-62-6

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5573-62-6 Usage

Chemical Properties

(ETHYLTHIO)TRIMETHYLSILANE is clear colorless liquid

Uses

(ETHYLTHIO)TRIMETHYLSILANE is used in the syntesis of azasilasulfonium salts.

General Description

(Ethylthio)trimethylsilane is reported to participate in the synthesis of adenophostin A and analog. It reacts with primary and secondary amines to yield aminosilane and ethanethiol.

Check Digit Verification of cas no

The CAS Registry Mumber 5573-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5573-62:
(6*5)+(5*5)+(4*7)+(3*3)+(2*6)+(1*2)=106
106 % 10 = 6
So 5573-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H14SSi/c1-5-6-7(2,3)4/h5H2,1-4H3

5573-62-6 Well-known Company Product Price

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  • Aldrich

  • (376035)  (Ethylthio)trimethylsilane  technical grade, 90%

  • 5573-62-6

  • 376035-1G

  • 453.96CNY

  • Detail

5573-62-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (Ethylthio)trimethylsilane

1.2 Other means of identification

Product number -
Other names ethylsulfanyl(trimethyl)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:5573-62-6 SDS

5573-62-6Relevant articles and documents

Reaction of O,S-bis(trimethylsilyl) (3,5-di-tert-butyl-4-hydroxyphenyl)phosphonodithioate with bis(ethylthio)diphenylgermane [1]

Nizamov,Popovich,Galimullina,Batyeva,Al'fonsov

, p. 1485 - 1486 (2002)

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Improved Direct Preparation of O-Trimethylsilyl Monothioacetals from Thiols and Carbonyl Compounds

Sassaman, Mark B.,Prakash, G.K.Surya,Olah, George A.

, p. 104 - 106 (2007/10/02)

Preparation of 1-alkylthio- or 1-phenylthio-1-trimethylsiloxyalkanes and -cycloalkanes directly from carbonyl compounds and thiols, is achieved using 1-trimethylsilylimidazole and trimethylsilyl triflate as a catalyst.

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