25434-84-8

Basic information

• Product Name: 1H-Indole-2-carboxylic acid, 5-chloro-3-phenyl-, hydrazide
• CAS NO: 25434-84-8
• Molecular Formula: C15H12ClN3O
• Molecular Weight: 285.733
• Mol File: 25434-84-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Indole-2-carboxylic acid, 5-chloro-3-phenyl-, hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-2-carboxylic acid, 5-chloro-3-phenyl-, hydrazide(25434-84-8)
• EPA Substance Registry System: 1H-Indole-2-carboxylic acid, 5-chloro-3-phenyl-, hydrazide(25434-84-8)

Safety Data

• Hazardous Substances Data: 25434-84-8(Hazardous Substances Data)

Upstream product

• 620-79-1 Ethyl 2-benzylacetoacetate 
• 24139-99-9 ethyl 2-[2-(4-chlorophenyl)hydrazinylidene]-3-phenylpropanoate 
• 21139-32-2 ethyl 3-phenyl-5-chloroindole-2-carboxylate 

Downstream Products

• 166328-86-5 5-chloro-3-phenyl-2-(5'-thioxo-1',3',4'-oxadiazol-2'-yl)indole 
• 316156-12-4 3-[N'-(5-chloro-3-phenyl-1H-indole-2-carbonyl)-hydrazino]-3-oxo-propionic acid ethyl ester 
• 226554-55-8 [5-(5-chloro-3-phenyl-1H-indol-2-yl)-2-thioxo-[1,3,4]oxadiazol-3-yl]-acetic acid ethyl ester 
• 211749-52-9 5-Chloro-3-phenyl-1H-indole-2-carboxylic acid N'-(2-hydroxy-benzyl)-hydrazide 
• 211749-58-5 5-Chloro-3-phenyl-1H-indole-2-carboxylic acid N'-(2-hydroxy-5-methyl-benzyl)-hydrazide 
• 70070-39-2 (5-chloro-3-phenyl-indol-2-yl)-carbamic acid ethyl ester 
• 70070-45-0 4-(5-chloro-3-phenyl-indol-2-yl)-semicarbazide 

Relevant articles and documents

Design, synthesis, antitubercular and antiviral properties of new spirocyclic indole derivatives

Abstract: A series of indole-based spirothiazolidinones have been designed, synthesized and evaluated, in vitro, for their antitubercular, antiviral, antibacterial, and antifungal activities. The structures of the new compounds were established by IR, su

Synthesis of Substituted 1,2,3,8-Tetrahydroindolobenzodiazepin-2-ones and 5,6,7,8-Tetrahydroindolobenzodiazepin-6-ones

Nitrosation (NaNO2/AcOH) of 2-phenylindoles (1a-d) and subsequent reduction of the resultant 3-nitroso-2-phenylindoles (2a-d) with sodium dithionite in alkali furnish the corresponding 3-aminoindoles (3a-d), which on condensation with ethyl chloroformate