1656-95-7

Basic information

• Product Name: 2,6-Dimethyl-3,5-dicyanopyridine
• Synonyms: 2,6-Dimethyl-3,5-dicyanopyridine;2,6-Dimethyl-3,5-pyridinedicarbonitrile;3,5-Dicyano-2,6-dimethylpyridine
• CAS NO: 1656-95-7
• Molecular Formula: C9H7N3
• Molecular Weight: 157.17
• Mol File: 1656-95-7.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,6-Dimethyl-3,5-dicyanopyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Dimethyl-3,5-dicyanopyridine(1656-95-7)
• EPA Substance Registry System: 2,6-Dimethyl-3,5-dicyanopyridine(1656-95-7)

Safety Data

• Hazardous Substances Data: 1656-95-7(Hazardous Substances Data)

Usage

General Description

2,6-Dimethyl-3,5-dicyanopyridine, also known as DMPA, is a chemical compound with the molecular formula C9H7N3. It is a yellow crystalline solid that is commonly used as a precursor in the synthesis of various organic compounds and pharmaceuticals. DMPA is a powerful nucleophile and is commonly used as a building block in organic chemistry. It is a highly versatile compound with numerous potential applications in the field of chemical synthesis and drug development. Additionally,

Upstream product

• 3274-36-0 2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarbonitrile 
• 61171-83-3 C₃₈H₃₀N₈ 
• 18998-44-2 α,α-Diphenyl-β-(2,4,6-tricyanophenyl)-hydrazyl 
• 19262-50-1 1,3,5-(2,4,6-Tricyanobenzotriyl)tris(N¹,N¹-diphenylhydrazyl)-Triradikal 
• 61171-77-5 C₂₁H₁₀F₂N₅ 
• 18998-42-0 N_.N-Diphenyl-N'-(3.5-dichlor-2.4.6-tricyan-phenyl)-hydrazyl 
• 18998-43-1 2.4.6-Tricyan-5-chlorphenyl-1.3-bis-(N_.N-diphenylhydrazyl) 
• 64-17-5 ethanol 
• 1118-61-2 3-Aminocrotononitrile 
• 122-51-0 orthoformic acid triethyl ester 
• 75-05-8 acetonitrile 
• 117772-29-9 4-<3-chloro-6-fluoro-2-(trifluoromethyl)phenyl>-1,4-dihydro-2,6-dimethylpyridine-3,5-dicarbonitrile 

Relevant articles and documents

Nitrogen-Rich Covalent Triazine Frameworks as High-Performance Platforms for Selective Carbon Capture and Storage

The search for new efficient physisorbents for gas capture and storage is the objective of numerous ongoing researches in the realm of functional framework materials. Here we present the CO2 and H2 uptake capacities of nitrogen rich

Electrosynthesis of pyridines from 'only acetonitrile'

2,4,6-Trimethylpyridine-3,5-dicarbonitrile has been obtained as the main product after the electrolysis of acetonitrile in the presence of tetrabutylammonium bisulfate as supporting electrolyte using a divided cell with a medium porosity diaphragm. 2,6-Dimethylpyridine-3,5-dicarbonitrile and 2,6-dimethylpyridine-3,4,5-tricarbonitrile have also been obtained in minor quantity. This process, which takes place with participation of both electrodes, is an example of a paired electrosynthesis.

A Novel, Base-induced Fragmentation of Hantzsch-type 4-Aryl-1,4-dihydropyridines

Hantzsch-type 1,4-dihydropyridine derivatives substituted with highly electron-deficient aryl groups in the 4-position, on treatment with a variety of basic reagents in non-hydroxylic solvents, undergo an unexpected and ready scission of the inter-ring bond to give the corresponding 4-unsubstituted pyridine and an arene derived from the original 4-substituent.The scope of the reaction has been investigated and possible mechanisms are discussed.