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Usage

Uses

Used in Pharmaceutical Industry:
3-AMINO-3-(2-PYRIDINYL)ACRYLONITRILE is used as a building block for the synthesis of various drugs and compounds, contributing to the development of new pharmaceuticals. Its reactivity and versatility play a significant role in creating innovative and effective medications.
Used in Specialty Chemicals Production:
In the realm of specialty chemicals, 3-AMINO-3-(2-PYRIDINYL)ACRYLONITRILE is utilized in the production process, enhancing the characteristics and performance of these chemicals for specific applications.
Used as a Reagent in Organic Synthesis:
3-AMINO-3-(2-PYRIDINYL)ACRYLONITRILE also serves as a reagent in organic synthesis, facilitating various chemical reactions that are essential in creating complex organic compounds. Its presence in this capacity underscores its importance in advancing chemical research and development.

InChI:InChI=1/C8H7N3/c9-5-4-7(10)8-3-1-2-6-11-8/h1-4,6H,10H2/b7-4-

Upstream product

• 100-70-9 2-Cyanopyridine 
• 75-05-8 acetonitrile 

Relevant academic research and scientific papers

2, 6 BISHETEROARYL-4-AMINOPYRIMIDINES AS ADENOSINE RECEPTOR ANTAGONISTS

4-Aminopyrimidine derivatives of formula (I) FORMULA heteroaryl groups, including pharmaceutically acceptable salts thereof, wherein R1 and R2 are adenosine A2A receptor antagonists useful in the treatment of movement disorders such as Parkinson's disease.

A new expedient route to 2,6-diaryl-3-cyano-4- (trifluoromethyl)pyridines

1-Aryl-4,4,4-trifluoro-1,3-butanediones 1 react with β-amino-β- arylacrylonitrile 2, readily available from acetonitrile with aryl nitriles in the presence of potassium t-butoxide, to afford the corresponding 2,6- diaryl-3-cyano-4-(trifluoromethyl)pyridin

CYCLOCONDENSATION OF α-OXOKETENE DITHIOACETALS WITH β-LITHIOAMINO-β-SUBSTITUTED ACRYLONITRILES: SYNTHESIS OF 2,6-SUBSTITUTED AND 5,6-ANNELATED 3-CYANO-4-(METHYLTHIO)PYRIDINES

The lithiated β-amino-β-substituted acrylonitriles 4a-d generated in situ by reaction of lithioacetonitrile with either acetonitrile or substituted nitriles undergo cyclocondensation with α-oxoketenedithioacetate through 1,4-addition to afford 2,6-substit

β Aminocinnamonitriles as potential antiinflammatory agents

A number of β aminocinnamonitriles have been prepared by the reaction of salts of acetonitrile and proprionitrile with benzonitrile. These materials were evaluated in the carrageenan antiinflammatory screen in Royal Hart, Wistar strain rats. Despite food weight gains with the parent molecule, β aminocinnamonitrile, only marginal activity was found in related compounds and some possible 'metabolites'.