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Silane, (3,3-diphenyl-1,2-propadienylidene)bis[trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116507-70-1

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116507-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116507-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,0 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 116507-70:
(8*1)+(7*1)+(6*6)+(5*5)+(4*0)+(3*7)+(2*7)+(1*0)=111
111 % 10 = 1
So 116507-70-1 is a valid CAS Registry Number.

116507-70-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,3-diphenyl-1-trimethylsilylpropa-1,2-dienyl)-trimethylsilane

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:116507-70-1 SDS

116507-70-1Downstream Products

116507-70-1Relevant academic research and scientific papers

Synthesis of nitrile oligomers through multiple anion capture reactions of allene dianions

Langer, Peter,Doering, Manfred,Seyferth, Dietmar,Goerls, Helmar

, p. 1948 - 1953 (2003)

Domino reactions between 1,1-dilithio-3,3-diphenylallene and nitriles resulted in the formation of products containing up to four nitrile molecules, representing the highest number to date of nitrile molecules involved in the formation of unambiguously ch

Direct transformation of silyl enol ethers into functionalized allenes

Langer, Peter,Doering, Manfred,Seyferth, Dietmar,Goerls, Helmar

, p. 573 - 584 (2007/10/03)

The first elimination reactions of silyl enol ethers to lithiated allenes are reported. These reactions allow a direct transformation of readily available silyl enol ethers into functionalized allenes. The action of three to four equivalents of lithium di

Synthesis and reactions of 2-alkylidene-1,3,4,-thiadiazolines and their selenium analogues

Choi, Nami,Tokitoh, Norihiro,Goto, Midori,Ando, Wataru

, p. 1189 - 1202 (2007/10/02)

2-Alkylidene-1,3,4-thiadiazoline 11a gave thioketone 16 (X=S) and acetylene derivative 17 on thermolysis via thiocarbonyl ylide, quantitatively. Pyrolysis of selenium analogue gave similar results. Allyl substituted 2-alkylidene-1,3,4-thiadiazolines 11a a

Effect of Silyl Substituent on Thermal Isomerization of Allene Episulfide. A New Aspect in Thioxyallyl Intermediate

Tokitoh, Norihiro,Choi, Nami,Ando, Wataru

, p. 2177 - 2180 (2007/10/02)

Kinetic studies on the thermal isomerization of 1,1-bis(trimethylsilyl)-3,3-diphenylallene 2-episulfide showed an attractive accelerating effect of silyl substituents attributable to the partial ionic nature of thioxyallyl intermediate.

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