76502-79-9

Basic information

• Product Name: 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-N-hydroxy-alpha-(4-morpholinyl)-1H-1,4-benzodiazepine-2-methanimine 4-oxide
• Synonyms: 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-N-hydroxy-alpha-(4-morpholinyl)-1H-1,4-benzodiazepine-2-methanimine 4-oxide
• CAS NO: 76502-79-9
• Molecular Weight: 418.855
• Mol File: 76502-79-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-N-hydroxy-alpha-(4-morpholinyl)-1H-1,4-benzodiazepine-2-methanimine 4-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-N-hydroxy-alpha-(4-morpholinyl)-1H-1,4-benzodiazepine-2-methanimine 4-oxide(76502-79-9)
• EPA Substance Registry System: 7-chloro-5-(2-fluorophenyl)-2,3-dihydro-N-hydroxy-alpha-(4-morpholinyl)-1H-1,4-benzodiazepine-2-methanimine 4-oxide(76502-79-9)

Safety Data

• Hazardous Substances Data: 76502-79-9(Hazardous Substances Data)

Upstream product

• 60656-76-0 7-chloro-5-(2-fluorophenyl)-2-nitromethylene-2H-1,3-dihydro-1,4-benzodiazepine 4-oxide 
• 76488-36-3 7-chloro-5-(2-fluorophenyl)-N-hydroxy-alpha-nitro-3H-1,4-benzodiazepine-2-methanimine 4-oxide 
• 76488-19-2 7-chloro-5-(2-fluorophenyl)-2-<4-<(hydroxyimino)methyl>morpholinyl>-3H-1,4-benzodiazepine 4-oxide 

Downstream Products

• 76488-32-9 8-chloro-6-(2-fluorophenyl)-1-methyl-3-morpholino-4H-imidazo<1,5-a><1,4>benzodiazepine 
• 76488-33-0 8-chloro-6-(2-fluorophenyl)-1-methyl-3-morpholino-4H-imidazo<1,5-a><1,4>benzodiazepine 5-oxide 
• 76488-31-8 8-chloro-6-(2-fluorophenyl)-3-morpholino-4H-imidazo<1,5-a><1,4>benzodiazepine 5-oxide 
• 87120-61-4 8-chloro-6-(2-fluorophenyl)-3-(morpholinyl)-4H-imidazo<1,5-a><1,4>benzodiazepine 
• 87120-71-6 7-chloro-5-(2-fluorophenyl)-1,3-dihydro-4'-(4-morpholinyl)spiro<2H>-1,4-benzodiazepine-2,5'-<2H>(5H)-oxazole) 4-oxide 

Relevant articles and documents

Quinazolines and 1,4-benzodiazepines. XCIII. (1). Synthesis of imidazo[1,5-a][1,4]benzodiazepines from nitrooximes

The displacement of the nitro group in nitrooximes by other nucleophiles was used to prepare various 2-(hydroxyimino)methyl- and 2-(methoxyimino)methyl-1,4-benzodiazepines. These compounds were converted to imidazo[1,5-α][1,4]benzodiazepines bearing a tertiary amine, methoxy or thiomethyl group in the 3-position.