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57097-41-3

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57097-41-3 Usage

Structure

A derivative of pyrrole with a carbonitrile group (CN) and a hydroxyl group (OH) attached to the molecule, as well as a methyl substituent (CH3) on the third carbon.

Properties

Potential biological activities, such as being an inhibitor of certain enzymes or a precursor to other bioactive molecules.

Applications

Potential uses in the pharmaceutical and agrochemical industries.

Additional research

Further research is needed to fully understand and exploit the properties and potential uses of this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 57097-41-3 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 57097-41:
(7*5)+(6*7)+(5*0)+(4*9)+(3*7)+(2*4)+(1*1)=143
143 % 10 = 3
So 57097-41-3 is a valid CAS Registry Number.

57097-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrole-2-carbonitrile,1-hydroxy-3-methyl-(9CI)

1.2 Other means of identification

Product number -
Other names N-Hydroxy-3-methylpyrrol-2-carbonitril

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:57097-41-3 SDS

57097-41-3Downstream Products

57097-41-3Relevant articles and documents

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.

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