75822-51-4

Basic information

• Product Name: 2-(4-BROMO-BENZOYL)-1H-INDOLE-3-CARBOXYLIC ACID
• Synonyms: 2-(4-BROMO-BENZOYL)-1H-INDOLE-3-CARBOXYLIC ACID
• CAS NO: 75822-51-4
• Molecular Formula: C₁₆H₁₀BrNO₃
• Molecular Weight: 344.16
• Mol File: 75822-51-4.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-BROMO-BENZOYL)-1H-INDOLE-3-CARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-BROMO-BENZOYL)-1H-INDOLE-3-CARBOXYLIC ACID(75822-51-4)
• EPA Substance Registry System: 2-(4-BROMO-BENZOYL)-1H-INDOLE-3-CARBOXYLIC ACID(75822-51-4)

Safety Data

• Hazardous Substances Data: 75822-51-4(Hazardous Substances Data)

Usage

Derivative of indole-3-carboxylic acid

It is a modified version of the parent compound indole-3-carboxylic acid This means that the compound has a similar structure to indole-3-carboxylic acid but has been altered by the addition or modification of functional groups.

Contains a bromo-benzoyl group

A bromine atom is attached to a benzoyl group (a benzene ring with a carbonyl group) This functional group imparts specific chemical properties to the compound, making it useful in various applications.

Used in research as a building block

It serves as an intermediate compound in the synthesis of more complex organic molecules and pharmaceuticals This means that the compound can be further modified or combined with other compounds to create new molecules with desired properties.

Valuable for the development of new drugs and materials

Its chemical properties make it a useful compound in the creation of novel pharmaceuticals and other materials This highlights the importance of 2-(4-Bromo-benzoyl)-1H-indole-3-carboxylic acid in the field of chemistry and drug development.

Proper safety protocols

It is important to handle this compound with care and follow proper safety procedures in a laboratory setting This indicates that the compound may have potential hazards or risks associated with its use, and it is essential to take precautions to ensure the safety of those working with it.

Upstream product

• 75822-43-4 1-(4-bromophenacyl)indole-2,3-dione 

Downstream Products

• 89671-78-3 (4-bromophenyl)(1H-indol-2-yl)methanone 
• 83749-69-3 4-(4-Bromo-phenyl)-2,5-dihydro-pyridazino[4,5-b]indol-1-one 
• 83749-80-8 4-(4-Bromo-phenyl)-1-chloro-5H-pyridazino[4,5-b]indole 

Relevant articles and documents

Syntheses of 1-alkyl-2-acylindoles, 1-alkyl-2-acylindole-3-carboxylic acids, and their esters, in superbasic media

2-Acylindoles and 2-acylindole-3-carboxylic acids are readily alkylated at the nitrogen atom by haloalkanes in a superbasic medium (DMSO + NaOH). For the carboxylic acids, this reaction may proceed either entirely at the nitrogen atom, or at both the the