210569-79-2

Basic information

• Product Name: N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide
• Synonyms: N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide
• CAS NO: 210569-79-2
• Molecular Weight: 493.198
• Mol File: 210569-79-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide(210569-79-2)
• EPA Substance Registry System: N-[(3-bromobenzylcarbamoyl)methyl]-3-(7-bromo-3H-indol-3-yl)propionamide(210569-79-2)

Safety Data

• Hazardous Substances Data: 210569-79-2(Hazardous Substances Data)

Upstream product

• 249757-17-3 [3-(7-bromo-3H-indol-3-yl)propionylamino]acetic acid methyl ester 
• 210889-34-2 3-(7-bromo-3H-indol-3-yl)propionic acid ethyl ester 
• 210569-70-3 3-(7-bromo-3H-indol-3-yl)propionic acid 
• 115666-21-2 7-bromo-1 H-indole-3-carbaldehyde 
• 51417-51-7 7-bromo-1H-indole 
• 39959-54-1 3-bromobenzylamine hydrochloride 
• 210569-72-5 [3-(7-bromo-3H-indol-3-yl)propionylamino]acetic acid 

Relevant articles and documents

Synthetic studies towards the synthesis of western and eastern chloropeptin I, II subunits

The western subunit (16-membered ring) was synthesized by the intramolecular SNAr reaction while the first 16-membered ring compound was obtained as a model of the eastern subunit via an intramolecular Ni0 mediated coupling reaction.