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 1H-Pyrrole-2-carbonitrile,1-hydroxy-3-methyl-(9CI).
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.
57097-41-3Relevant 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
