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Silane, trimethyl[1-(phenylthio)nonyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75340-08-8

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75340-08-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75340-08-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,4 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75340-08:
(7*7)+(6*5)+(5*3)+(4*4)+(3*0)+(2*0)+(1*8)=118
118 % 10 = 8
So 75340-08-8 is a valid CAS Registry Number.

75340-08-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenylthio-1-trimethylsilylnonane

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:75340-08-8 SDS

75340-08-8Relevant academic research and scientific papers

New one carbon homologation reagents utilizing electrochemical oxidation of organosilicon compounds

Yoshida,Matsunaga,Murata,Isoe

, p. 615 - 624 (2007/10/02)

Phenylthio(trimethylsilyl)methane, phenylthiobis(trimethylsilyl)methane, methoxy(trimethylsilyl)-methane, and methoxybis(trimethylsilyl)methane are deprotonated and the resulting anions are alkylated with electrophiles such as organic halides. The alkylation products are readily converted into the corresponding dimethyl acetals or methyl esters by electrochemical oxidation in methanol.

PHENYLTHIOMETHYLTRIMETHYLSILANE: A NEW FORMYL ANION SYNTHON

Kocienski, Philiph J.

, p. 1559 - 1562 (2007/10/02)

α-Phenylthioalkyltrimethylsilanes, readily prepared by the alkylation of phenylthiomethyltrimethylsilane with alkyl halides or epoxides, can be converted to O-trimethylsilyl hemithioacetals via a Sila-Pummerer Rearrangement of the corresponding sulfoxides.The O-trimethylsilyl hemithioacetals are readily hydrolyzed to aldehydes.

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