1612872-85-1

Basic information

• Product Name: N-(1-acetylindolin-7-yl)-4-(tert-butyl)benzenesulfonamide
• Synonyms: N-(1-acetylindolin-7-yl)-4-(tert-butyl)benzenesulfonamide
• CAS NO: 1612872-85-1
• Molecular Weight: 372.488
• Mol File: 1612872-85-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(1-acetylindolin-7-yl)-4-(tert-butyl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1-acetylindolin-7-yl)-4-(tert-butyl)benzenesulfonamide(1612872-85-1)
• EPA Substance Registry System: N-(1-acetylindolin-7-yl)-4-(tert-butyl)benzenesulfonamide(1612872-85-1)

Safety Data

• Hazardous Substances Data: 1612872-85-1(Hazardous Substances Data)

Upstream product

• 16078-30-1 1-Acetyl-2,3-dihydro-1H-indole 
• 179029-65-3 4-(tert-butyl)benzenesulfonyl azide 
• 496-15-1 1-indoline 
• 6292-59-7 4-tert-butylbenzenesulphonamide 
• 563-63-3 silver(I) acetate 
• 64-19-7 acetic acid 

Relevant articles and documents

Method for preparing N-arylsulfonamide from indoline and arylsulfonamide

The invention discloses a method for preparing N-arylsulfonamide from indoline and arylsulfonamide, belonging to the technical field of C-H bond activation and functionalization catalyzed by a transition metal. The method includes adding 1-acetyl indoline

Ruthenium-catalyzed C7 amidation of indoline C-H bonds with sulfonyl azides

A ruthenium-catalyzed direct C7 amidation of indoline C-H bonds with sulfonyl azides was developed. This procedure allows the synthesis of a variety of 7-amino-substituted indolines, which are useful in pharmaceutical. The good functional tolerances, as well as the mild conditions, are prominent feature of this method.