91714-51-1

Basic information

• Product Name: Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-
• CAS NO: 91714-51-1
• Molecular Formula: C15H9BrClNO
• Molecular Weight: 334.6
• Mol File: 91714-51-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-(91714-51-1)
• EPA Substance Registry System: Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)-(91714-51-1)

Safety Data

• Hazardous Substances Data: 91714-51-1(Hazardous Substances Data)

Usage

General Description

Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)- is an organic compound with a complex chemical structure. It is classified as a ketone, featuring a carbonyl group bonded to a phenyl ring and an indole ring with bromine and chlorine substituents. Methanone, (4-bromophenyl)(3-chloro-1H-indol-7-yl)- may be used in research and pharmaceutical development due to its unique structure and potential biological activity. Its specific properties and potential applications would require further investigation and analysis.

Upstream product

• 623-00-7 4-bromobenzenecarbonitrile 
• 91714-41-9 (4-bromophenyl)(2,3-dihydro-1H-indol-7-yl)methanone 
• 496-15-1 1-indoline 
• 91714-50-0 7-(4-bromobenzoyl)-1-hydro-indole 

Downstream Products

• 91713-91-6 7-(4-bromobenzoyl)-1,3-dihydro-2H-indol-2-one 

Relevant articles and documents

A preparation method of a bromfenac sodium sesquihydrate compound

A preparation method of a bromfenac sodium sesquihydrate compound is disclosed. The method includes steps of subjecting a compound of a formula 3 and an aqueous solution of sodium hydroxide to a hydrolysis reaction; directly subjecting the reaction solution to suction filtration after the reaction is completed; collecting a filtrate; adding sodium chloride or sodium bicarbonate into the filtrate;washing solid precipitated after the sodium chloride or sodium bicarbonate is added with saturated brine and acetone; performing recrystallization using a mixed solvent that is water/acetone, water/glycol dimethyl ether or water/ethylene glycol; and washing the solid obtained by recrystallization with acetone to obtain the bromfenac sodium sesquihydrate compound that is the compound of the formula4. The method is simple to operate and stable in process, and the obtained bromfenac sodium sesquihydrate compound is yellow solid with extremely high purity.