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1H-Pyrrole-2-carbonitrile,1-hydroxy-5-methyl-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

57097-40-2

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57097-40-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57097-40-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,0,9 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57097-40:
(7*5)+(6*7)+(5*0)+(4*9)+(3*7)+(2*4)+(1*0)=142
142 % 10 = 2
So 57097-40-2 is a valid CAS Registry Number.

57097-40-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-cyano-1-hydroxy-5-methylpyrrole

1.2 Other means of identification

Product number -
Other names 2-Cyano-1-hydroxy-5-methylpyrrol

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:57097-40-2 SDS

57097-40-2Relevant academic research and scientific papers

Photolysis of 2-Azidopyridine 1-Oxides. A Convenient Synthesis of 1,2-Oxazines

Abramovitch, Rudolph A.,Dupuy, Claude

, p. 36 - 37 (2007/10/02)

Photolysis or thermolysis of 2-azidopyridine 1-oxides (1) in benzene leads to nitrogen-elimination and ring-opening followed by recyclisation to give 6-cyano-1,2-oxazines (5) which then usually rearrange thermally to 2-cyano-1-hydroxypyrroles (2); the photolyses provide a ready, high-yield route to 1,2-oxazines.

Process for the synthesis of N-hydroxypyrroles, N-hydroxyimidazoles, and derivatives thereof

-

, (2008/06/13)

A process is described for the preparation of N-hydroxypyrrole-2-carbonitriles, N-hydroxyimidazole-2-carbonitriles, pyrrole-2-carbonitriles, and 3-substituted-2, 3-dihydro-2-pyrrolones by thermally decomposing 2-azidoheteroaromatic N-oxides. In the proces

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