113243-75-7

Basic information

• Product Name: 2-methyl-N-(2-morpholin-4-ylethyl)-4-(3-nitrophenyl)-6-phenylpyridine-3-carboxamide
• CAS NO: 113243-75-7
• Molecular Formula: C₂₅H₂₆N₄O₄
• Molecular Weight: 446.4983
• Mol File: 113243-75-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 591.6°C at 760 mmHg
• Flash Point: 311.6°C
• Density: 1.23g/cm³
• Vapor Pressure: 5.71E-14mmHg at 25°C
• Refractive Index: 1.604
• CAS DataBase Reference: 2-methyl-N-(2-morpholin-4-ylethyl)-4-(3-nitrophenyl)-6-phenylpyridine-3-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methyl-N-(2-morpholin-4-ylethyl)-4-(3-nitrophenyl)-6-phenylpyridine-3-carboxamide(113243-75-7)
• EPA Substance Registry System: 2-methyl-N-(2-morpholin-4-ylethyl)-4-(3-nitrophenyl)-6-phenylpyridine-3-carboxamide(113243-75-7)

Safety Data

• Hazardous Substances Data: 113243-75-7(Hazardous Substances Data)

Upstream product

• 2038-03-1 4-(2-AMINOETHYL)MORPHOLINE 
• 122274-57-1 N-(2-morpholinoethyl)acetoacetamide 
• 123819-45-4 1,4-dihydro-3-(2-morpholinoethylcarbamoyl)-2-methyl-4-(3-nitrophenyl)-6-phenylpyridine 
• 614-48-2 (E)-3-nitrochalcone 
• 113293-82-6 ethyl 2-methyl-4-(3-nitrophenyl)-6-phenylpyridine-3-carboxylate 
• 113293-86-0 2-methyl-4-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylic acid 
• 614-48-2 3-nitrochalcone 
• 1025977-21-2 2-Methyl-4-(3-nitro-phenyl)-6-phenyl-nicotinoyl chloride 
• 113293-78-0 ethyl 1,4-dihydro-2-methyl-4-(3-nitrophenyl)-6-phenyl-3-pyridinecarboxylate 

Relevant articles and documents

Studies on cerebral protective agents. IV. Synthesis of novel 4-arylpyridine and 4-arylpyridazine derivatives with anti-anoxic activity

In a search for new cerebral protective agents, a series of 4-(3- or 4-nitrophenyl)-6-phenylpyridines (or pyridazines) and 2-(3-nitrophenyl)-6-phenylpyridines, possessing an amino moiety at the C-3 position of the pyridine (or pyridazine) ring, were synth

Morpholine containing pyridine compounds, compositions and use

An N-containing heterocyclic compound of the formula: STR1 wherein R1 is lower alkyl optionally substituted with hydroxy, halogen or a heterocyclic group, carboxy, esterified carboxy, carbamoyl optionally substituted with heterocyclic(lower)alk