40899-92-1

Basic information

• Product Name: ethyl 1-(phenylsulfonyl)-1H-indole-2-carboxylate
• Synonyms: ethyl 1-(phenylsulfonyl)-1H-indole-2-carboxylate
• CAS NO: 40899-92-1
• Molecular Weight: 329.376
• Mol File: 40899-92-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: ethyl 1-(phenylsulfonyl)-1H-indole-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1-(phenylsulfonyl)-1H-indole-2-carboxylate(40899-92-1)
• EPA Substance Registry System: ethyl 1-(phenylsulfonyl)-1H-indole-2-carboxylate(40899-92-1)

Safety Data

• Hazardous Substances Data: 40899-92-1(Hazardous Substances Data)

Upstream product

• 541-41-3 chloroformic acid ethyl ester 
• 40900-03-6 1-(benzenesulfonyl)-2-lithioindole 
• 3770-50-1 2-carbethoxyindole 
• 98-09-9 benzenesulfonyl chloride 
• 120-72-9 indole 
• 40899-71-6 1-benzenesulfonylindole 
• 5344-90-1 2-Aminobenzyl alcohol 
• 197847-57-7 N-[2-(hydroxymethyl)phenyl]benzenesulfonamide 
• 151721-32-3 N-benzenesulfonyl-o-aminobenzaldehyde 

Downstream Products

• 40899-93-2 1-(phenylsulfonyl)-1H-indole-2-carboxylic acid 
• 1265231-79-5 [5-amino-1-(2-methyl-1H-benzimidazol-5-yl)-1H-pyrazol-4-yl]-(1-benzenesulfonyl-1H-indol-2-yl) methanone 
• 1265229-25-1 [5-amino-1-(2-methyl-1H-benzimidazol-5-yl)-1H-pyrazol-4-yl](1H-indol-2-yl)methanone 
• 540740-51-0 1-benzenesulfonyl-1H-indole-2-carboxylic acid hydrazide 

Relevant articles and documents

N-(piperidin-4-yl)-1H-indole-2-carboxamide derivatives, preparation method thereof, and pharmaceutical composition for use in preventing or treating Urotensin-Ⅱ receptor activity related diseases containing the same as an active ingredient

The present invention relates to N-(piperidin-4-yl)-1H-indole-2-carboxamide derivatives, a preparation method thereof, and a pharmaceutical composition for preventing or treating urotensin-II receptor activity-related diseases comprising the same as activ

One-pot synthesis of 1-phenylsulfonyl-2-aroylindoles

Interaction of phenylsulfonyl-2-aminobenzaldehyde with 2-bromo-1- phenylethanones in the presence of K2CO3 followed by acid-catalyzed dehydration led to the formation of 1-phenylsulfonyl-2-aroylindoles.Copyright Taylor & Francis Group, LLC.

Novel indolyl aryl sulfones active against HIV-1 carrying NNRTI resistance mutations: Synthesis and SAR studies

The potent anti-HIV-1 activities of L-737,126 (2) and PAS sulfones prompted us to design and test against HIV-1 in acutely infected MT-4 cells a number of novel 1- and 3-benzenesulfonylindoles. Indoles belonging to the 1-benzenesulfonyl series were found