1390627-09-4

Basic information

• Product Name: 3-(4-bromophenyl)-5-p-tolyl-4,5-dihydroindeno[1,2-c][1,2]diazepin-6(1H)-one
• Synonyms: 3-(4-bromophenyl)-5-p-tolyl-4,5-dihydroindeno[1,2-c][1,2]diazepin-6(1H)-one
• CAS NO: 1390627-09-4
• Molecular Weight: 443.343
• Mol File: 1390627-09-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3-(4-bromophenyl)-5-p-tolyl-4,5-dihydroindeno[1,2-c][1,2]diazepin-6(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-bromophenyl)-5-p-tolyl-4,5-dihydroindeno[1,2-c][1,2]diazepin-6(1H)-one(1390627-09-4)
• EPA Substance Registry System: 3-(4-bromophenyl)-5-p-tolyl-4,5-dihydroindeno[1,2-c][1,2]diazepin-6(1H)-one(1390627-09-4)

Safety Data

• Hazardous Substances Data: 1390627-09-4(Hazardous Substances Data)

Upstream product

• 22946-44-7 1-(4-bromophenyl)-3-p-tolylprop-2-en-1-one 
• 1390626-93-3 2-(3-(4-bromophenyl)-3-oxo-1-p-tolylpropyl)-2H-indene-1,3-dione 
• 606-23-5 1H-indene-1,3(2H)-dione 

Relevant articles and documents

A novel and highly efficient protocol for the synthesis of chalcone based 1,2-diazepine and 1,2-oxazepine derivatives

A novel and highly efficient protocol is described for the synthesis of chalcone based 1,2-diazepine and 1,2-oxazepine derivatives. Under neat condition, the mixing and grinding of 1,5-diketones and hydrazine gave the cyclocondensation products in quantitative yields within 10-20 min at room temperature. Similarly, novel chalcone based 1,2-oxazepines were synthesized in excellent yields (85-88%) in 2-3 h at refluxed by the condensation of 1,5-diktones and hydroxylamine hydrochloride in water-ethanolic base.