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3-Methyl-2-pyridin-2-yl-butyronitrile is an organic compound with the chemical formula C10H12N2. It is a derivative of pyridine, featuring a methyl group at the 3-position and a butyronitrile group at the 2-position. 3-METHYL-2-PYRIDIN-2-YL-BUTYRONITRILE is characterized by its nitrile functional group, which is a carbon-nitrogen triple bond, and its pyridine ring, which is a six-membered aromatic ring with one nitrogen atom. It is a colorless to pale yellow liquid with a molecular weight of 160.22 g/mol. This chemical is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is important to handle 3-METHYL-2-PYRIDIN-2-YL-BUTYRONITRILE with care, as it may have potential health and environmental impacts, and appropriate safety measures should be taken during its use and storage.

32081-58-6

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32081-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32081-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,0,8 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32081-58:
(7*3)+(6*2)+(5*0)+(4*8)+(3*1)+(2*5)+(1*8)=86
86 % 10 = 6
So 32081-58-6 is a valid CAS Registry Number.

32081-58-6SDS

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 3-methyl-2-pyridin-2-ylbutanenitrile

1.2 Other means of identification

Product number -
Other names 2-Pyridineacetonitrile,a-(1-methylethyl)

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:32081-58-6 SDS

32081-58-6Relevant academic research and scientific papers

Mild and practical method for the α-arylation of nitriles with heteroaryl halides

Klapars, Artis,Waldman, Jacob H.,Campos, Kevin R.,Jensen, Mark S.,McLaughlin, Mark,Chung, John Y. L.,Cvetovich, Raymond J.,Chen, Cheng-Yi

, p. 10186 - 10189 (2007/10/03)

A mild and transition-metal-free method for theα-arylation of a liphatic nitriles with activated heteroaryl halides was developed using NaHMDS o r KHMDS as base at ambient temperature. The key to the success of this method is generation of the nitrile anion in the presence of the heteroaryl halide. The method is applicable to both primary and secondary carbonitriles and a wide range of heteroaryl halides. Selective monoarylation was observed with primary carbonitriles. The operational simplicity and the mild reaction conditions add to the value of this methodas a practical alternative to the preparation of α-heteroaryl carbonitriles.

A New Synthesis of Aryl Hetaryl Ketones via SRN1 Reaction of Halogenated Heterocycles withPotassiophenylacetonitrile Followed by Phase-Transfer Catalyzed Decyanation

Hermann, Christine K. F.,Sachdeva, Yesh P.,Wolfe, James F.

, p. 1061 - 1065 (2007/10/02)

Reaction of halogenated pyridines, quinolines, pyrimidines, and pyrazines with potassiophenylacetonitrile (5) in liquid ammonia under near-uv irradiation affords secondary nitriles, which then undergo oxidative decyanation under phase-transfer catalytic conditions to afford aryl hetaryl ketones in excellent yields.

Synthesis and antiarrhythmic activity of new [(dialkylamino)alkyl]pyridylacetamides

Bernhart,Condamine,Demarne,Roncucci,Gagnol,Gautier,Serre

, p. 451 - 455 (2007/10/02)

The synthesis of new [(dialkylamino)alkyl]pyridylacetamides is reported. These compounds displayed a potent antiarrhythmic activity, as demonstrated on a model of myocardial infarction in the conscious dog. Structure-activity relationships are discussed within a series of 22 homologues, comparing relative antiarrhythmic properties and cardiac side effects. One of these compounds, 15, has been selected as a candidate for clinical evaluation in man.

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