65032-86-2

Basic information

• Product Name: 3-Pyridinecarboxamide, 1,4,5,6-tetrahydro-1-(phenylmethyl)-
• CAS NO: 65032-86-2
• Molecular Formula: C13H16N2O
• Molecular Weight: 216.283
• Mol File: 65032-86-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-Pyridinecarboxamide, 1,4,5,6-tetrahydro-1-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pyridinecarboxamide, 1,4,5,6-tetrahydro-1-(phenylmethyl)-(65032-86-2)
• EPA Substance Registry System: 3-Pyridinecarboxamide, 1,4,5,6-tetrahydro-1-(phenylmethyl)-(65032-86-2)

Safety Data

• Hazardous Substances Data: 65032-86-2(Hazardous Substances Data)

Upstream product

• 670-54-2 ethenetetracarbonitrile 
• 110-86-1 pyridine 
• 952-92-1 1-Benzyl-1,4-dihydronicotinamide 
• 5096-13-9 1-benzylnicotinamide chloride 
• 996-82-7 sodium diethylmalonate 
• 111080-52-5 1-benzyl-3-bromo-3-carbamoyl-1-piperideinium bromide 

Downstream Products

• 16969-45-2 pyridin-1-ium 
• 670-54-2 tetracyanoethylene radical-anion 
• 14778-29-1 1,1,2,2,-tetracyanoethane 
• 111080-52-5 1-benzyl-3-bromo-3-carbamoyl-1-piperideinium bromide 
• 111080-62-7 1-benzyl-1,4,5,6-tetrahydronicotinamide hydrobromide 
• 111080-56-9 1-benzyl-2-(1-phenylethylimino)methylpyrrolidine-2-carboxamide 
• 111080-55-8 1-benzyl-2-phenylethylhydrazonomethylpyrrolidine-2-carboxamide 
• 111080-54-7 1-benzyl-2-(dimethoxymethyl)pyrrolidine-2-carboxamide 
• 111080-60-5 1-benzyl-4a-bromooctahydrofuro<3,4-b>pyridin-5-one 
• 111080-61-6 1-benzyl-4a-bromooctahydropyrrolo<3,4-b>pyridin-5-one 
• 111080-53-6 1-benzyl-2-formylpyrrolidine-2-carboxamide 
• 111080-59-2 1-benzyl-3-bromopiperidine-3-carboxamide 
• 111080-58-1 1-benzyl-2-methylpyrrolidine-2-carboxamide 
• 13076-43-2 3-(aminocarbonyl)-1-benzylpyridinium bromide 

Relevant articles and documents

Better than Nature: Nicotinamide Biomimetics That Outperform Natural Coenzymes

The search for affordable, green biocatalytic processes is a challenge for chemicals manufacture. Redox biotransformations are potentially attractive, but they rely on unstable and expensive nicotinamide coenzymes that have prevented their widespread expl

EVIDENCE FOR A SINGLE ELECTRON TRANSFER ACTIVATION IN THE HYDRIDE TRANSFER FROM AN NADH MODEL COMPOUND TO TETRACYANOETHYLENE

New evidence for a stepwise mechanism which requires a single electron transfer activation in the hydride transfer from an NADH model compound, 1-benzyl-1,4-dihydronicotinamide (BNAH), to tetracyanoethylene (TCNE) has been presented based on the effects of pyridine on the stoichiometry of the overall reaction, the rate constant, and the kinetic isotope effect.