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Propanedinitrile, phenyl[(trimethylsilyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42202-48-2

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42202-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42202-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,0 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 42202-48:
(7*4)+(6*2)+(5*2)+(4*0)+(3*2)+(2*4)+(1*8)=72
72 % 10 = 2
So 42202-48-2 is a valid CAS Registry Number.

42202-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-2-trimethylsilyloxypropanedinitrile

1.2 Other means of identification

Product number -
Other names dicyanotrimethylsiloxymethylbenzene

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:42202-48-2 SDS

42202-48-2Relevant academic research and scientific papers

An Efficient Synthesis of Dinitrile Derivatives by the Reaction of Oxime Esters or Acid Anhydrides with Cyanotrimethylsilane Catalyzed by La(OiPr)3

Fujii, Akiko,Sakaguchi, Satoshi,Ishii, Yasutaka

, p. 6209 - 6212 (2007/10/03)

The reaction of oxime esters with cyanotrimethylsilane (Me3SiCN) under the influence of a catalytic amount of lanthanide compounds produced α-trimethylsilyloxydinitrile derivatives in excellent yields accompanied with the formation of trimethylsilyl oxime ethers. Among the lanthanoid catalysts examined, La(OiPr)3 was found to be the best catalyst. The reaction seems to proceed through the formation of acyl cyanides as intermediates, followed by the addition of Me3SiCN to them. Additionally, the reaction of acetic anhydride with Me3SiCN catalyzed by La(OiPr)3 gave 1-trimethylsilyloxyethane dinitrile. Thus, various α-trimethylsilyloxydinitriles were synthesized in good yields by allowing oxime esters or acid anhydrides to react with Me3SiCN in the presence of a catalytic amount of La(OiPr)3.

A NEW APPROACH TO ARYLMALONONITRILES

Yamaguchi, Shunro,Araki, Hisashi,Hanafusa, Terukiyo

, p. 685 - 688 (2007/10/02)

Arylmalononitriles were prepared from the corresponding benzoyl chlorides by three reaction steps.Treatment of the starting substances with cyanotrimethylsilane in the presence of pyridine gave dicyanotrimethylsiloxymethylbenzenes, which were transformed

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