91714-41-9

Basic information

• Product Name: (4-bromophenyl)(indolin-7-yl)methanone
• Synonyms: (4-bromophenyl)(indolin-7-yl)methanone;bromfenac sodiumImpurity f
• CAS NO: 91714-41-9
• Molecular Formula: C₁₅H₁₂BrNO
• Molecular Weight: 302.16588
• Mol File: 91714-41-9.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-bromophenyl)(indolin-7-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-bromophenyl)(indolin-7-yl)methanone(91714-41-9)
• EPA Substance Registry System: (4-bromophenyl)(indolin-7-yl)methanone(91714-41-9)

Safety Data

• Hazardous Substances Data: 91714-41-9(Hazardous Substances Data)

Usage

Description

(4-Bromophenyl)(indolin-7-yl)methanone is an organic compound that features a bromophenyl group and an indolin-7-yl group attached to a central methanone moiety. This unique structure endows it with specific chemical properties that make it a valuable intermediate in the synthesis of various organic compounds.

Uses

Used in Pharmaceutical Industry:
(4-Bromophenyl)(indolin-7-yl)methanone is used as a reactant in the preparation of 2-amino-3-benzoylphenylacetic acid and analogs, which are important intermediates in the synthesis of pharmaceutical compounds. These intermediates can be further modified or used to produce drugs with potential therapeutic applications, such as anti-inflammatory, analgesic, or antipyretic agents.
Used in Chemical Research:
In the field of chemical research, (4-bromophenyl)(indolin-7-yl)methanone serves as a versatile building block for the development of new organic compounds with potential applications in various industries. Its unique structure allows for the exploration of novel chemical reactions and the synthesis of new molecules with desired properties.
Used in Material Science:
(4-Bromophenyl)(indolin-7-yl)methanone can also be utilized in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. Its incorporation into polymers, coatings, or other materials can lead to the creation of innovative products with enhanced performance characteristics.

Upstream product

• 496-15-1 1-indoline 
• 623-00-7 4-bromobenzenecarbonitrile 

Downstream Products

• 91714-50-0 7-(4-bromobenzoyl)-1-hydro-indole 
• 91714-43-1 (4-Bromo-phenyl)-(5-chloro-2,3-dihydro-1H-indol-7-yl)-methanone 
• 91714-47-5 (5-bromo-2,3-dihydro-1H-indol-7-yl)(4-bromophenyl)methanone 
• 405275-36-7 (4-bromo-phenyl)-(1-ethyl-1H-indol-7-yl)-methanone 
• 91714-58-8 (4-bromophenyl)(5-chloro-1H-indol-7-yl)methanone 
• 91714-66-8 (5-Bromo-1H-indol-7-yl)-(4-bromo-phenyl)-methanone 
• 91714-51-1 (4-Bromo-phenyl)-(3-chloro-1H-indol-7-yl)-methanone 
• 91714-59-9 (3-bromo-5-chloro-1H-indol-7-yl)(4-bromophenyl)-methanone 
• 91714-67-9 (4-Bromo-phenyl)-(3,5-dibromo-1H-indol-7-yl)-methanone 
• 91714-34-0 7-(4-bromobenzoyl)-5-chloro-1,3-dihydro-2H-indol-2-one 
• 91714-38-4 5-Bromo-7-(4-bromo-benzoyl)-1,3-dihydro-indol-2-one 
• 91715-43-4 Sodium; [2-amino-5-bromo-3-(4-bromo-benzoyl)-phenyl]-acetate 
• 91715-33-2 Sodium; [2-amino-3-(4-bromo-benzoyl)-5-chloro-phenyl]-acetate 

Relevant articles and documents

Antifungal and/or antiparasitic pharmaceutical composition and novel indole derivatives as active principle of such a composition

The present invention relates to novel indole derivatives, their method of preparation and their pharmacological activity as antimycotic and/or antiparasitic compounds.

Antiinflammatory agents. 3. Synthesis and pharmacological evaluation of 2-amino-3-benzoylphenylacetic acid and analogues

A series of substituted derivatives of 2-amino-3-benzoylphenylacetic acid (amfenac) has been synthesized and evaluated for antiinflammatory, analgesic, and cyclooxygenase inhibiting activity. Several derivatives including 4'-chloro, 4'-bromo and 5-chloro, 4'-bromo were more potent than indomethacin in these assays.