36729-28-9

Basic information

• Product Name: 2,3-diphenyl-1H-indole-5-carboxylic acid
• Synonyms: 2,3-diphenyl-1H-indole-5-carboxylic acid
• CAS NO: 36729-28-9
• Molecular Weight: 313.356
• Mol File: 36729-28-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2,3-diphenyl-1H-indole-5-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-diphenyl-1H-indole-5-carboxylic acid(36729-28-9)
• EPA Substance Registry System: 2,3-diphenyl-1H-indole-5-carboxylic acid(36729-28-9)

Safety Data

• Hazardous Substances Data: 36729-28-9(Hazardous Substances Data)

Usage

General Description

2,3-diphenyl-1H-indole-5-carboxylic acid is a chemical compound with the molecular formula C21H15NO2. It is an indole derivative, which is a heterocyclic organic compound containing a six-membered benzene ring fused with a five-membered nitrogen-containing pyrrole ring. 2,3-diphenyl-1H-indole-5-carboxylic acid has potential applications in the pharmaceutical industry, particularly in the development of new drugs. It may act as a precursor or intermediate in the synthesis of pharmaceuticals and other organic compounds. Its properties and potential uses make it an interesting target for further research and development in the field of medicinal chemistry.

Upstream product

• 24589-77-3 4-hydrazinobenzoic acid hydrochloride 
• 501-65-5 diphenyl acetylene 
• 150-13-0 4-amino-benzoic acid 
• 451-40-1 phenyl benzyl ketone 
• 619-67-0 4-Hydrazinobenzoic acid 

Downstream Products

• 61566-69-6 4-amino-3-benzoyl-benzoic acid 
• 36729-31-4 2,3-diphenyl-indole-5-carboxylic acid ethyl ester 

Relevant articles and documents

URAZOLE COMPOUNDS

The present invention relates to a compound of formula (I) or a stereoisomer, enantiomer, racemic, or tautomer thereof, (I) wherein R1, R2, R3, R4, R5, R6, R7, L1 and Q1 have the meaning defined in the claims and the description. The present invention also relates to a process for the preparation of the compound of formula (I). The present invention also relates to the use of a compound of formula (I) as an in situ precursor of a triazolinedione reagent for the functionalization of enes, dienes, aryl and heteroaryl systems via the ene reactions, Diels-Alder reactions, and electrophilic aromatic substitution reactions of said reagent. The present invention also relates to the use of a compound of formula (I) in polymers, membranes, adhesives, foams, sealants, molded articles, films, extruded articles, fibers, elastomers, polymer based additives, pharmaceutical and biomedical products, varnishes, paints, coatings, inks, composite material, organic LEDs, organic semiconductors, conducting organic polymers, or 3D printed articles. The present invention also relates to article comprising said compound of formula (I) and to a process for reshaping and/or repairing said article.

AZAINDOLE DERIVATIVES

Compounds of the formula (I), in which X1, X2, X3, X4, R1, R2, R3 and R4 have the meanings indicated in Claim 1, are inhibitors of tyrosine kinases, in particular Met