1056989-91-3

Basic information

• Product Name: 6,12-bis(4-bromophenyl)dibenzo[b,f][1,5]diazocine
• Synonyms: 6,12-bis(4-bromophenyl)dibenzo[b,f][1,5]diazocine
• CAS NO: 1056989-91-3
• Molecular Weight: 516.234
• Mol File: 1056989-91-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6,12-bis(4-bromophenyl)dibenzo[b,f][1,5]diazocine(CAS DataBase Reference)
• NIST Chemistry Reference: 6,12-bis(4-bromophenyl)dibenzo[b,f][1,5]diazocine(1056989-91-3)
• EPA Substance Registry System: 6,12-bis(4-bromophenyl)dibenzo[b,f][1,5]diazocine(1056989-91-3)

Safety Data

• Hazardous Substances Data: 1056989-91-3(Hazardous Substances Data)

Upstream product

• 1411676-86-2 C₁₄H₈BrNO₂ 
• 142472-05-7 2-(4-bromo-benzoyl)-benzoyl chloride 
• 2159-40-2 2-(4-bromobenzoyl)benzoic acid 
• 1264292-44-5 2-(4-bromobenzoyl)benzoyl azide 
• 108-86-1 bromobenzene 
• 85-44-9 phthalic anhydride 

Relevant articles and documents

Antiaromatic compounds and organic light-emitting device comprising the same

The present invention relates to an anti-aromatic compound and an organic light emitting device comprising the same. According to one embodiment of the present invention, provided is an anti-aromatic compound represented by chemical formula 1. The organic light emitting device comprising the anti-aromatic compound can obtain high efficiency and long lifespan properties.COPYRIGHT KIPO 2016

A rapid and efficient access to diaryldibenzo[b,f][1,5]diazocines

2-Benzoylbenzoyl azides undergo facile cyclization under acidic conditions to give substituted dibenzo[b,f][1,5]-diazocines in good yields. This approach shortens the synthetic steps toward these compounds as compared with conventional methods. The mechanism of the diazocine synthesis is assumed to proceed by an unprecedented intermolecular [2 + 2] cyclization.