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[2,2'-Bipyridine]-5-carbonitrile, 6-methyl-4-phenylis a chemical compound characterized by a bipyridine core with a carbonitrile functional group at the 5-position and a methyl-phenyl group at the 6-position. This unique structure endows it with valuable properties and potential applications in various fields, such as organic and coordination chemistry, catalysis, material science, and pharmaceuticals.

133617-72-8

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133617-72-8 Usage

Uses

Used in Organic and Coordination Chemistry:
[2,2'-Bipyridine]-5-carbonitrile, 6-methyl-4-phenylis used as a ligand for metal catalysts and complexes in the field of organic and coordination chemistry. Its unique structure and reactivity contribute to the formation of coordination complexes with interesting properties and potential applications.
Used in Catalysis:
In the catalysis industry, [2,2'-Bipyridine]-5-carbonitrile, 6-methyl-4-phenylis employed as a ligand to enhance the performance of metal catalysts. Its presence can improve the efficiency and selectivity of catalytic reactions, making it a valuable component in the development of new catalytic systems.
Used in Material Science:
[2,2'-Bipyridine]-5-carbonitrile, 6-methyl-4-phenylis utilized as a building block for the synthesis of novel materials with unique properties. Its incorporation into various materials can lead to improved performance in areas such as conductivity, stability, and responsiveness to external stimuli.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, [2,2'-Bipyridine]-5-carbonitrile, 6-methyl-4-phenylhas been studied for its potential applications in the development of new drugs and drug delivery systems. Its unique structure and reactivity make it a promising candidate for the synthesis of bioactive molecules and the design of targeted drug delivery systems.

Check Digit Verification of cas no

The CAS Registry Mumber 133617-72-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,6,1 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 133617-72:
(8*1)+(7*3)+(6*3)+(5*6)+(4*1)+(3*7)+(2*7)+(1*2)=118
118 % 10 = 8
So 133617-72-8 is a valid CAS Registry Number.

133617-72-8SDS

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 2-methyl-4-phenyl-6-pyridin-2-ylpyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 3-cyano-2-methyl-4-phenyl-6-(2-pyridyl)pyridine

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:133617-72-8 SDS

133617-72-8Downstream Products

133617-72-8Relevant academic research and scientific papers

The Vinylogous Mannich Reaction: An Efficient Access to Substituted Nicotinonitriles

Winter, Andreas,Risch, Nikolaus

, p. 1959 - 1964 (2007/10/03)

A straightforward method for the preparation of substituted nicotinonitriles has been developed. Starting from conjugated β-enaminonitriles and iminium salts, this methodology establishes a convenient access to 6-aryl- (5), 6-amino- (16) and 6-carboxylic ester-substituted derivatives 14 and as well to acetic acid-substituted pyrroles 12.

Synthesis of 4,6-Disubstituted 2-Methylpyridines and their 3-Carboxamides

Shibata, Katsuyoshi,Katsuyama, Isamu,Izoe, Hideaki,Matsui, Masaki,Muramatsu, Hiroshige

, p. 277 - 281 (2007/10/02)

A new one-pot synthesis of title compounds by the reactions of α,β-unsaturated carbonyl compounds with β-aminocrotononitrile in the presence of sodium hydroxide is described.

Synthesis of 3-Cyano-2-methylpyridines Substituted with Heteroaromatics

Shibata, Katsuyoshi,Katsuyama, Isamu,Matsui, Masaki,Muramatsu, Hiroshiga

, p. 161 - 165 (2007/10/02)

A series of title compounds were easily prepared by the sonication of α,β-unsaturated carbonyl compound in acetonitril in the presence of potassium t-butoxide.

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