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Cyclopentanecarbonitrile, 2-methyl-3-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112496-86-3

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112496-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112496-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,9 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112496-86:
(8*1)+(7*1)+(6*2)+(5*4)+(4*9)+(3*6)+(2*8)+(1*6)=123
123 % 10 = 3
So 112496-86-3 is a valid CAS Registry Number.

112496-86-3SDS

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 2-methyl-3-oxocyclopentane-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-methyl 3-oxo 1-cyclopentanecarbonitrile

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:112496-86-3 SDS

112496-86-3Relevant academic research and scientific papers

SYNTHESES OF NITRILE AND METHYL ESTER CORRESPONDING TO (dl)-SARKOMYCIN AND OF RELATED COMPOUNDS.

Froissant, Jacques,Vidal, Joeelle,Guibe-Jampel, Eryka,Huet, Francois

, p. 317 - 322 (2007/10/02)

Nitrile 6a and ester 12 corresponding to (dl)-sarkomycin, 6- and 7-membered rings analogue nitriles 6b, 6c, and 3-methyl substituted nitrile 6d were prepared.Conjugate addition of cyanotrimethyl silane to cyclic α-enones gave 3-trimethylsiloxy 2-cycloalkene carbonitriles.Their alkylation with chloromethyl phenyl sulfide followed by oxone oxidation to sulfones and sulfinic acid elimination on basic alumina led to α-methylene carbonyl compounds.Obtention of the ester 12 involved acetalization of 3-oxo 2-phenylthiomethyl cyclopentane carbonitrile, basic hydrolysis into acid, deacetalization, esterification, oxidation and elimination of sulfinic acid.

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