89587-01-9

Basic information

• Product Name: 1H-1,5-Benzodiazepine, 2,3-dihydro-2-methyl-2,4-bis(4-nitrophenyl)-
• CAS NO: 89587-01-9
• Molecular Formula: C22H18N4O4
• Molecular Weight: 402.409
• Mol File: 89587-01-9.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: 1H-1,5-Benzodiazepine, 2,3-dihydro-2-methyl-2,4-bis(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,5-Benzodiazepine, 2,3-dihydro-2-methyl-2,4-bis(4-nitrophenyl)-(89587-01-9)
• EPA Substance Registry System: 1H-1,5-Benzodiazepine, 2,3-dihydro-2-methyl-2,4-bis(4-nitrophenyl)-(89587-01-9)

Safety Data

• Hazardous Substances Data: 89587-01-9(Hazardous Substances Data)

Upstream product

• 100-19-6 (4-nitrophenyl)ethanone 
• 55626-14-7 2-methyl-2,4-diphenyl-2,3-dihydro-1H-1,5-benzo[b][1,4]diazepine 
• 95-54-5 1,2-diamino-benzene 
• 39145-59-0 o-phenylenediamine hydrochloride 

Relevant articles and documents

Method for preparing benzodinitrogen compound by using gold complex

The invention relates to a method for preparing a benzodinitrogen compound by using a gold complex, which comprises the following step of: reacting an o-phenylenediamine compound and alkyne as raw materials with a gold complex containing a diphosphine ort

One-pot, water-mediated, H2O2-HCl catalyzed synthesis of benzazepines

One-pot, multicomponent H2O2-HCl catalyzed system was employed for the synthesis of a series of benzazepine compounds. The implemented procedure oxidized the carbon-nitrogen bonds and produced benzazepines, while integrating diamines and substituted keton

An efficient facile and one-pot synthesis of benzodiazepines and chemoselective 1,2-disubstituted benzimidazoles using a magnetically retrievable Fe3O4 nanocatalyst under solvent free conditions

Benzodiazepine and chemoselective 1,2-disubstituted benzimidazole derivatives were synthesized by the condensation reaction of o-phenylenediamine with ketones and aryl aldehydes using Fe3O4 nanoparticles as a recyclable catalyst unde