142472-05-7

Basic information

• Product Name: 2-(4-bromo-benzoyl)-benzoyl chloride
• Synonyms: 2-(4-bromo-benzoyl)-benzoyl chloride
• CAS NO: 142472-05-7
• Molecular Weight: 323.573
• Mol File: 142472-05-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(4-bromo-benzoyl)-benzoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-bromo-benzoyl)-benzoyl chloride(142472-05-7)
• EPA Substance Registry System: 2-(4-bromo-benzoyl)-benzoyl chloride(142472-05-7)

Safety Data

• Hazardous Substances Data: 142472-05-7(Hazardous Substances Data)

Upstream product

• 2159-40-2 2-(4-bromobenzoyl)benzoic acid 
• 108-86-1 bromobenzene 
• 85-44-9 phthalic anhydride 

Downstream Products

• 2059-99-6 2-(4-bromo-benzoyl)-benzoic acid amide 
• 1264292-44-5 2-(4-bromobenzoyl)benzoyl azide 
• 1056989-91-3 6,12-bis(4-bromophenyl)dibenzo[b,f][1,5]diazocine 
• 1140-17-6 2-amino-4'-bromobenzophenone 

Relevant articles and documents

Biomimetic Asymmetric Reduction of Tetrasubstituted Olefin 2,3-Disubstituted Inden-1-ones with Chiral and Regenerable NAD(P)H Model CYNAM

Because of the formidable development of the asymmetric reduction of tetrasubstituted olefins, an effective method is in urgent demand. Herein, through the biomimetic protocol of the coenzyme NAD(P)H, the reduction of tetrasubstituted olefin 2,3-substitut

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.