292636-12-5

Basic information

• Product Name: 7-AMINO-4-CHLORO INDOLE
• Synonyms: 7-AMINO-4-CHLORO INDOLE;1H-Indol-7-aMine, 4-chloro-;4-Chloro-1H-indol-7-aMine
• CAS NO: 292636-12-5
• Molecular Formula: C₈H₇ClN₂
• Molecular Weight: 166.61
• Mol File: 292636-12-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 7-AMINO-4-CHLORO INDOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 7-AMINO-4-CHLORO INDOLE(292636-12-5)
• EPA Substance Registry System: 7-AMINO-4-CHLORO INDOLE(292636-12-5)

Safety Data

• Hazardous Substances Data: 292636-12-5(Hazardous Substances Data)

Usage

General Description

7-Amino-4-chloro indole is a chemical compound with the molecular formula C8H7ClN2. It is a derivative of indole and is used in the synthesis of various pharmaceutical compounds. 7-AMINO-4-CHLORO INDOLE is known for its potential applications in the field of medicinal chemistry and drug discovery. Its unique molecular structure and properties make it an important building block for the development of novel drugs and bioactive molecules. 7-Amino-4-chloro indole is also used as a research reagent in biochemical and biomedical studies, contributing to advancements in the understanding and treatment of various diseases.

Upstream product

• 96831-52-6 4-chloro-7-nitroindole 
• 41513-04-6 2-chloro-5-bromonitrobenzene 
• 126811-29-8 7-bromo-4-chloro-1H-indole 

Downstream Products

• 292635-70-2 N-(4-chloro-1H-indol-7-yl)-4-nitro-benzenesulfonamide 
• 292635-80-4 N-(4-chloro-1H-indol-7-yl)-4-cyano-benzenesulfonamide 
• 165669-23-8 N-(3,4-dichloro-1H-indole-7-yl)-4-nitrobenzenesulfonamide 
• 131637-49-5 7-Chloro-1-{3-[4-(2-chloro-phenyl)-9-methyl-6H-1-thia-5,7,8,9a-tetraaza-cyclopenta[e]azulen-2-yl]-prop-2-ynyl}-1H-pyrrolo[1,2,3-de]quinoxalin-2-one 

Relevant articles and documents

A focused compound library of novel N-(7-indolyl)benzenesulfonamides for the discovery of potent cell cycle inhibitors

A series of compounds containing an N-(7-indolyl)benzenesulfonamide pharmacophore was synthesized and evaluated as a potential antitumor agent. Cell cycle analysis with P388 murine leukemia cells revealed that there were two different classes of potent cell cycle inhibitors; one disrupted mitosis and the other caused G1 accumulation. Herein described is the SAR summary of the substituent patterns on this pharmacophore template. (C) 2000 Elsevier Science Ltd. All rights reserved.