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Silane, dimethyl[(1E)-2-phenylethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119873-75-5

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119873-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119873-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,7 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119873-75:
(8*1)+(7*1)+(6*9)+(5*8)+(4*7)+(3*3)+(2*7)+(1*5)=165
165 % 10 = 5
So 119873-75-5 is a valid CAS Registry Number.

119873-75-5SDS

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 (E)-dimethyl(2-phenylethenyl)silane

1.2 Other means of identification

Product number -
Other names (E)-

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:119873-75-5 SDS

119873-75-5Relevant academic research and scientific papers

A general synthesis of vinylic silyl hydrides using nickel catalysis. Applications to the syntheses of silylene-tethered conjugated polymers

Chen, Ruey-Min,Luh, Tien-Yau

, p. 1197 - 1206 (2007/10/03)

Treatment of benzylic or allylic dithioacetals with Me2((i)PrO)SiCH2MgCl in the presence of NiCl2(PPh3)2 catalyst yielded the corresponding i-propoxy(vinyl)silanes which are reduced with LiAlH4/

Enantioselective Synthesis of Epoxides: Sharpless Epoxidation of Alkenysilanols

Chan, T. H.,Chen, L. M.,Wang, D.

, p. 1280 - 1281 (2007/10/02)

Sharpless epoxidation of the alkenylsilanol (6) followed by protodesilylation gave styrene oxide with high enentiomeric excess.

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