1127562-54-2

Basic information

• Product Name: (5-bromoindol-1-yl)phenylmethanone
• Synonyms: (5-bromoindol-1-yl)phenylmethanone
• CAS NO: 1127562-54-2
• Molecular Weight: 300.154
• Mol File: 1127562-54-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (5-bromoindol-1-yl)phenylmethanone(CAS DataBase Reference)
• NIST Chemistry Reference: (5-bromoindol-1-yl)phenylmethanone(1127562-54-2)
• EPA Substance Registry System: (5-bromoindol-1-yl)phenylmethanone(1127562-54-2)

Safety Data

• Hazardous Substances Data: 1127562-54-2(Hazardous Substances Data)

Upstream product

• 10075-50-0 5-bromo-1H-indole 
• 98-88-4 benzoyl chloride 

Downstream Products

• 1436591-34-2 (E)-3-(1-benzoyl-5-bromo-1H-indol-2-yl)acrylic acid 
• 1436591-13-7 (E)-ethyl 3-(1-benzoyl-5-bromo-1H-indol-2-yl)acrylate 
• 1436591-05-7 (E)-methyl 3-(1-benzoyl-5-bromo-1H-indol-2-yl)acrylate 
• 1127562-74-6 C₂₃H₂₀N₂O₄S 

Relevant articles and documents

A novel microwave-irradiated solvent-free 3-acylation of indoles on alumina

A simple and efficient 3-acylation of indoles under microwave-heated and solvent-free conditions is developed. This general procedure uses neutral Al2O3 as a new, green and reusable catalyst giving good to high yields within short reaction times. Utilizing such an environmentally- benign methodology, a variety of indoles bearing electron-releasing or electron-withdrawing groups were conveniently acylated.

Highly regioselective C2-alkenylation of indoles Uusing the N-benzoyl directing group: An efficient Ru-catalyzed coupling reaction

A highly regioselective alkenylation of indole at the C2-position has been achieved using the Ru(II) catalyst by employing a directing group strategy. This strategy offers rare selectivity for the alkenylation N-benzoylindole at the C-2 position in the pr