35982-93-5 Usage
Description
3-Pyridinecarbonitrile, 1,2-dihydro-2-oxo-5-phenyl-, also known as a dihydropyridine derivative and a nitrile compound, is a chemical compound with the molecular formula C12H9N3O. It features a pyridine ring, a nitrile group, and a phenyl group, making it a versatile building block in organic chemistry. 3-Pyridinecarbonitrile, 1,2-dihydro-2-oxo-5-phenylis often used in the synthesis of pharmaceuticals and other organic compounds and has been studied for its potential biological activities and pharmacological properties.
Uses
Used in Pharmaceutical Industry:
3-Pyridinecarbonitrile, 1,2-dihydro-2-oxo-5-phenylis used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Organic Chemistry Research:
In the field of organic chemistry, 3-Pyridinecarbonitrile, 1,2-dihydro-2-oxo-5-phenylis utilized as a versatile building block for the creation of complex organic compounds, facilitating advancements in chemical synthesis and the discovery of novel chemical entities.
Used in Biological and Pharmacological Studies:
3-Pyridinecarbonitrile, 1,2-dihydro-2-oxo-5-phenylis employed in biological and pharmacological research to explore its potential biological activities and pharmacological properties, which may lead to the identification of new therapeutic agents or contribute to a better understanding of molecular mechanisms in biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 35982-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,8 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35982-93:
(7*3)+(6*5)+(5*9)+(4*8)+(3*2)+(2*9)+(1*3)=155
155 % 10 = 5
So 35982-93-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H8N2O/c13-7-10-6-11(8-14-12(10)15)9-4-2-1-3-5-9/h1-6,8H,(H,14,15)
35982-93-5Relevant articles and documents
Reaction mechanism of vinamidinium salts and cyanoacetamide derivatives
Yang, Jiabin,Su, Guoqiang,Ren, Yu,Chen, Yang
, p. 41 - 43 (2015)
The mechanism of formation of a pyridin-2(1H )-one synthesised from vinamidinium salts and cyanoacetamide derivatives is illustrated through the preparation and characterisation of a key intermediate.
Design, synthesis and structure-activity relationship studies of morpholino-1H-phenalene derivatives that antagonize Mcl-1/Bcl-2
Li, Xiangqian,Liang, Xiaomeng,Song, Ting,Su, Pengchen,Zhang, Zhichao
, p. 5738 - 5746 (2015/02/02)
We report herein characteristic studies of Mcl-1 and Bcl-2 dual inhibitors. It was found that a protruding carbonyl group forming hydrogen bond with R263 plays a predominant role compared with the hydrophobic group that occupies the p2 pocket. A series of dual inhibitors representing different parts of the morpholino-1H-phenalene were designed, synthesized and evaluated.
Substituted 6-phenyl-5,6,7,8-tetrahydro-1,2,4-triazolo-[4,3-a]pyridines
-
, (2008/06/13)
This disclosure describes novel substituted 6-phenyl-5,6,7,8-tetrahydro-1,2,4-triazolo[4,3-a]pyridines and their use as agents for treating anxiety.