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2-Chloro-6-phenylnicotinonitrile, a chemical compound with the molecular formula C12H7ClN2, is a white to off-white solid. It is classified as a nitrile, characterized by a carbon triple-bonded to a nitrogen atom, and is also halogenated, containing a chlorine atom. 2-Chloro-6-phenylnicotinonitrile is known for its reactivity and specificity in chemical reactions, making it a versatile and important building block in the chemical industry, primarily used as an intermediate in the production of pharmaceuticals and agrochemicals.

163563-64-2

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163563-64-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-6-phenylnicotinonitrile is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity allow for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-6-phenylnicotinonitrile serves as an essential intermediate for the production of agrochemicals. Its incorporation into these products contributes to the creation of effective solutions for pest control and crop protection.
Used in Organic Synthesis:
2-Chloro-6-phenylnicotinonitrile is utilized as a versatile building block in organic synthesis processes. Its presence in the synthesis of pyridine derivatives and other complex organic molecules highlights its importance in the development of novel chemical entities with potential applications in various fields.
Used in Chemical Research:
2-Chloro-6-phenylnicotinonitrile is also employed in chemical research for studying reaction mechanisms and exploring new synthetic routes. Its reactivity and structural features make it a valuable tool for advancing the understanding of chemical reactions and the development of innovative synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 163563-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,5,6 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 163563-64:
(8*1)+(7*6)+(6*3)+(5*5)+(4*6)+(3*3)+(2*6)+(1*4)=142
142 % 10 = 2
So 163563-64-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H7ClN2/c13-12-11(8-14)10(6-7-15-12)9-4-2-1-3-5-9/h1-7H

163563-64-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-6-phenylnicotinonitrile

1.2 Other means of identification

Product number -
Other names 2-Chloro-4-phenylnicotinonitrile

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:163563-64-2 SDS

163563-64-2Relevant academic research and scientific papers

Natural phosphate and potassium fluoride doped natural phosphate as new catalysts for the Vilsmeir-Haack type reaction

Zahouily, Mohamed,Bahlaouan, Bouchaib,Abrouki, Younes,Salah, Mohamed,Bahlaouan, Ouafa,Rayadh, Ahmed,Aadil, Mina,Sebti, Said

, p. 34 - 36 (2007/10/03)

The catalytic activity of the inexpensive natural- or potassium fluoride doped phosphates as bases was evaluated in a Vilsmeier-Haack type reaction. High efficiency, in term of chemical yields and reaction rates was found in the preparation of 2-chlor-3-c

New synthetic routes to 3-, 5-, and 6-aryl-2-chloropyridines

Church,Trust,Albright,Powell

, p. 3750 - 3758 (2007/10/02)

The efficient synthesis of 3-, 5-, and 6-aryl-2-chloropyridines via the facile preparation of 5-(dimethylamino)aryl-substituted pentadienyl nitriles and cyclization with hydrochloric acid is described. This approach allows for the introduction of other electron-withdrawing substituents on the pyridine ring as well as the preparation of the desired unsubstituted arylpyridines. Some differences in the rates of cyclization of the pentadienyl nitriles as well as the yields of chloropyridines were observed that depended on the position and degree of substitution in the aryl substituent. The arylpentadienyl nitriles 5 and 6 could also be converted directly into the corresponding 2-aminopyridines.

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