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1-(TRIMETHYLSILYL)CYCLOPROPYL PHENYL SULFIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74379-74-1

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74379-74-1 Usage

Physical properties

bp 64 °C/0.1 mmHg; d 0.991 g cm?3.

Check Digit Verification of cas no

The CAS Registry Mumber 74379-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,3,7 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 74379-74:
(7*7)+(6*4)+(5*3)+(4*7)+(3*9)+(2*7)+(1*4)=161
161 % 10 = 1
So 74379-74-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H18SSi/c1-14(2,3)12(9-10-12)13-11-7-5-4-6-8-11/h4-8H,9-10H2,1-3H3

74379-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-(1-phenylsulfanylcyclopropyl)silane

1.2 Other means of identification

Product number -
Other names -

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:74379-74-1 SDS

74379-74-1Relevant academic research and scientific papers

A General Procedure for Preparing α-Lithiosilanes. Generalization of the Peterson Olefination

Cohen, Theodore,Sherbine, James P.,Matz, James R.,Hutchins, Robert R.,McHenry, Barry M.,Willey, Paul R.

, p. 3245 - 3252 (2007/10/02)

A particularly convenient method for the preparation of α-lithiosilanes consists of the reductive lithiation of diphenyl thioacetals or thioketals with lithium 1-(dimethylamino)naphthalenide, treatment of the resulting anion with trimethylsilyl chloride,

SILICON IN ORGANIC SYNTHESIS-17 CYCLOPENTANNULATION BY THERMOLYSIS OF (1-TRIMETHYLSILYLCYCLOPROPYL)ETHYLENES-THE 1-TRIMETHYLSILYLCYCLOPROPYL ANION

Paquette, Leo A.,Wells, Gregory J.,Horn, Keith A.,Yan, Tu-Hsin

, p. 913 - 924 (2007/10/02)

Several alternatives for preparing (1-trimethylsilylcyclopropyl)ethylenes have been examined.Although 1-lithio-1-(trimethylsilyl)ethylene does add satisfactorily to carbonyl compounds and the subsequent Simmons-Smith cyclopropanation provides the desired

SILICON IN ORGANIC SYNTHESIS. 13. THE 1-TRIMETHYLSILYLCYCLOPROPYL ANION AND ITS FORMAL EQUIVALENT

Paquette, Leo A.,Horn, Keith A.,Wells, Gregory J.

, p. 259 - 262 (2007/10/02)

Reaction of lithio 1-trimethylsilylcyclopropane or its formal equivalent with carbonyl compounds leads to carbinols which dehydrate without rearrangement.Other attempts to induce ring expansion of the silicon substituted three-membered ring by i

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