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Silane, trimethyl[2-phenyl-1-(phenylthio)ethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59176-57-7

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59176-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59176-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,7 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59176-57:
(7*5)+(6*9)+(5*1)+(4*7)+(3*6)+(2*5)+(1*7)=157
157 % 10 = 7
So 59176-57-7 is a valid CAS Registry Number.

59176-57-7SDS

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 (Z)-1-phenylthio-1-trimethylsilyl-2-phenylethylene

1.2 Other means of identification

Product number -
Other names β-Phenylthio-β-(trimethylsilyl)-styrol

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:59176-57-7 SDS

59176-57-7Relevant academic research and scientific papers

A highly stereoselective synthesis of (z)-1-phenylthio-1-trialkyl- silylalkenes from 1-methoxy-1-phenylthio-1 - trialkylsilylalkanes

Mandai, Tadakatsu,Kohama, Makoto,Sato, Hiroaki,Kawada, Mikio,Tsuji, Jiro

, p. 4553 - 4562 (2007/10/02)

A new method for the highly stereoselective synthesis of (Z) -1-phenylthio-1-trialkylsilylalkenes 3 by the elimination of methanol from 1-methoxy-1-phenylthio-1-trialkylsilylalkane 2 in organic solvents is described.

A Facile Stereoselective Synthesis of α-Silyl Substituted Vinyl Sulfides

Han, Dong Il,Oh, Dong Young

, p. 267 - 271 (2007/10/02)

A facile one-pot synthesis of α-silyl substituted vinyl sulfides which involves the chlorination of 1-phenylthio-1-silylalkanes followed by dehydrochlorination is described.

ELIMINATIVE DEOXYGENATION: THE FACILE FORMATION OF α-TRIMETHYLSILYL VINYL SULFIDES FROM SULFOXIDES

Miller, R. D.,Haessig, R.

, p. 5351 - 5354 (2007/10/02)

Synthetically useful α-trimethylsilyl vinyl sulfides are generated in high yields by deoxygenation of the corresponding sulfoxides in the presence of excess LDA and trimethylsilyl chloride.

HETEROCONJUGATE ADDITION OF LITHIUM ALKYLS TO SUBSTITUTED HETERO-OLEFINS CONJUGATED WITH SULFUR AND SILICON ATOMS

Isobe, Minoru,Kitamura, Masato,Goto, Toshio

, p. 331 - 334 (2007/10/02)

Lithium alkyls and a lithiated sulfone carbanion readily added to the substituted hetero-olefins conjugated with silicon and sulfone-sulfur atoms among other combination of the third (or fourth) row hetero atoms, e.g.Si, Se and S.

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