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6-(4-FLUOROPHENYL)-1,2-DIHYDRO-2-OXOPYRIDINE-3-CARBONITRILE is a heterocyclic organic compound with the molecular formula C13H8FN3O. It is a pyridine derivative featuring a cyanide group attached to the third carbon atom. 6-(4-FLUOROPHENYL)-1,2-DIHYDRO-2-OXOPYRIDINE-3-CARBONITRILE possesses diverse biological activities and is considered a valuable candidate for pharmaceutical and agrochemical applications due to its potential to be utilized as an intermediate in the synthesis of various pharmaceuticals and other organic compounds. Its structural features also make it suitable for further chemical modifications to enhance its biological properties.

31755-80-3

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31755-80-3 Usage

Uses

Used in Pharmaceutical Industry:
6-(4-FLUOROPHENYL)-1,2-DIHYDRO-2-OXOPYRIDINE-3-CARBONITRILE is used as an intermediate in the synthesis of various pharmaceuticals for its potential to contribute to the development of new drugs with enhanced biological properties. Its unique structure allows for further chemical modifications, which can improve the efficacy and selectivity of the resulting pharmaceuticals.
Used in Agrochemical Industry:
In the agrochemical field, 6-(4-FLUOROPHENYL)-1,2-DIHYDRO-2-OXOPYRIDINE-3-CARBONITRILE is used as an intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its diverse biological activities make it a promising candidate for the development of novel agrochemicals with improved performance and selectivity.
Further Research and Development:
6-(4-FLUOROPHENYL)-1,2-DIHYDRO-2-OXOPYRIDINE-3-CARBONITRILE is used as a subject for further research and development to explore its full potential and applications. This includes investigating its biological properties, evaluating its safety and efficacy, and identifying new areas where it can be applied. Ongoing studies aim to uncover additional uses and optimize its synthesis process for industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 31755-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,5 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31755-80:
(7*3)+(6*1)+(5*7)+(4*5)+(3*5)+(2*8)+(1*0)=113
113 % 10 = 3
So 31755-80-3 is a valid CAS Registry Number.

31755-80-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4-fluorophenyl)-2-oxo-1H-pyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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:31755-80-3 SDS

31755-80-3Relevant academic research and scientific papers

Discovery and structure-activity relationships study of novel thieno[2,3-b]pyridine analogues as hepatitis C virus inhibitors

Wang, Ning-Yu,Zuo, Wei-Qiong,Xu, Ying,Gao, Chao,Zeng, Xiu-Xiu,Zhang, Li-Dan,You, Xin-Yu,Peng, Cui-Ting,Shen, Yang,Yang, Sheng-Yong,Wei, Yu-Quan,Yu, Luo-Ting

, p. 1581 - 1588 (2014/03/21)

Current treatment for hepatitis C is barely satisfactory, there is an urgent need to develop novel agents for combating hepatitis C virus infection. This study discovered a new class of thieno[2,3-b]pyridine derivatives as HCV inhibitors. First, a hit compound characterized by a thienopyridine core was identified in a cell-based screening of our privileged small molecule library. And then, structure activity relationship study of the hit compound led to the discovery of several potent compounds without obvious cytotoxicity in vitro (12c, EC50 = 3.3 μM, SI >30.3, 12b, EC50 = 3.5 μM, SI >28.6, 10l, EC50 = 3.9 μM, SI >25.6, 12o, EC 50 = 4.5 μM, SI >22.2, respectively). Although the mechanism of them had not been clearly elucidated, our preliminary optimization of this class of compounds had provided us a start point to develop new anti-HCV agents.

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