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Silane, 2-butene-1,4-diylbis[dimethylphenyl-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103517-76-6

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103517-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103517-76-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,1 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103517-76:
(8*1)+(7*0)+(6*3)+(5*5)+(4*1)+(3*7)+(2*7)+(1*6)=96
96 % 10 = 6
So 103517-76-6 is a valid CAS Registry Number.

103517-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-1,4-bis(dimethylphenylsilyl)-2-butene

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:103517-76-6 SDS

103517-76-6Downstream Products

103517-76-6Relevant academic research and scientific papers

Synthesis of trans-1,4-Bis-2-butenes

Richter, Wolf Juergen,Neugebauer, Brigitte

, p. 1059 - 1060 (1985)

The reaction of chlorodimethylorganosilanes -2-butenes in 55-88percent yield.The amount of (Z)-isomer ranges f

Formation of 1,4-Disilyl-2-butenes from Vinyl Grignard Reagent and Chlorosilanes Catalyzed by a Titanocene Complex

Watabe, Hiroyasu,Terao, Jun,Kambe, Nobuaki

, p. 1733 - 1735 (2001)

(matrix presented) Symmetrical 1,4-disilyl-2-butenes 1 have been prepared by the reaction of vinyl Grignard reagent with chlorosilanes. This reaction proceeds efficiently in the presence of a catalytic amount of titanocene dichloride at 0 °C in THF. When dichlorodiphenylsilane was used, 1,1-diphenyl-1-silacyclo-3-pentene 2 was obtained in a good yield.

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