56149-29-2

Basic information

• Product Name: 2-Chloro-N-phenylnicotinamide
• Synonyms: 2-Chloro-N-phenyl-3-pyridinecarboxamide
• CAS NO: 56149-29-2
• Molecular Formula: C₁₂H₉ClN₂O
• Molecular Weight: 232.67
• Product Categories: pharmacetical
• Mol File: 56149-29-2.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 308.9 °C at 760 mmHg
• Flash Point: 140.6 °C
• Appearance: /
• Density: 1.341 g/cm³
• Vapor Pressure: 0.000661mmHg at 25°C
• Refractive Index: 1.657
• CAS DataBase Reference: 2-Chloro-N-phenylnicotinamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Chloro-N-phenylnicotinamide(56149-29-2)
• EPA Substance Registry System: 2-Chloro-N-phenylnicotinamide(56149-29-2)

Safety Data

• Hazardous Substances Data: 56149-29-2(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H9ClN2O/c13-11-10(7-4-8-14-11)12(16)15-9-5-2-1-3-6-9/h1-8H,(H,15,16)

Upstream product

• 49609-84-9 2-Chloronicotinoyl chloride 
• 62-53-3 aniline 
• 100-46-9 benzylamine 
• 2942-59-8 2-chloronicotinic acid 
• 609-71-2 2-hydroxy-3-carboxypyridine 

Downstream Products

• 856211-83-1 2-(2-diethylamino-ethoxy)-nicotinic acid anilide 
• 879720-79-3 2-(2-dimethylamino-ethoxy)-nicotinic acid anilide 
• 56149-34-9 2-morpholin-4-yl-N-phenyl-nicotinamide 
• 125038-50-8 2-(4-Fluoro-phenoxy)-N-phenyl-nicotinamide 
• 52099-85-1 N-phenyl-2-phenylamino-3-pyridinecarboxamide 
• 879720-77-1 2-(2-piperidino-ethoxy)-nicotinic acid anilide 
• 859284-32-5 2-(2-dibutylamino-ethoxy)-nicotinic acid anilide 
• 138506-97-5 1,3-diphenylpyrido<2,3-d>pyrimidine-2(1H), 4(3H)-dione 
• 138506-99-7 1,3-diphenyl-2,3-dihydropyrido<2,3-d>pyrimidin-4(1H)-one 
• 1339548-95-6 2-hydrazinyl-N-phenylnicotinamide 
• 1352083-03-4 2-azido-N-phenylnicotinamide 
• 1352083-04-5 3-chloro-2-phenyl-2H-pyrazolo[3,4-b]pyridine 
• 1352083-05-6 3-chloro-2-phenyl-2H-pyrazolo[3,4-b]pyridine-7-oxide 
• 1352083-06-7 3-chloro-2-phenyl-2H-pyrazolo[3,4-b]pyridine-6-carbonitrile 

Relevant articles and documents

Expedited access to thieno[3,2-c]quinolin-4(5H)-ones and benzo[h]-1,6-naphthyridin-5(6H)-ones via a continuous flow photocyclization method

A single-step continuous flow method has been developed that gives expedited access to complex heterocycles via an intramolecular photochemical cyclization. Herein we report the first examples of the photochemically-induced generation of thieno[3,2-c]quin

ALPHA 7 NICOTINIC ACETYLCHOLINE RECEPTOR ALLOSTERIC MODULATORS, THEIR DERIVATIVES AND USES THEREOF

The present application is related to compounds represented by Formula I, which are novel positive allosteric modulators of al nAChRs. The application also discloses the treatment of disorders that are responsive to enhancement of acetylcholine action on al nAChRs in a mammal by administering an effective amount of a compound of Formula I.

VIRAL POLYMERASE INHIBITORS

The present invention relates to viral polymerase inhibitors of formula (I), salts, N-oxides, racemates, enantiomers and isomers thereof, processes for their preparation and their use in the treatment of Flaviviridae viral infections such as Hepatitis C v