102192-77-8

Basic information

• Product Name: 1-Benzyloxymethyl-3,4-bis-(7-chloro-1H-indol-3-yl)-pyrrole-2,5-dione
• CAS NO: 102192-77-8
• Molecular Weight: 516.383
• Mol File: 102192-77-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-Benzyloxymethyl-3,4-bis-(7-chloro-1H-indol-3-yl)-pyrrole-2,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Benzyloxymethyl-3,4-bis-(7-chloro-1H-indol-3-yl)-pyrrole-2,5-dione(102192-77-8)
• EPA Substance Registry System: 1-Benzyloxymethyl-3,4-bis-(7-chloro-1H-indol-3-yl)-pyrrole-2,5-dione(102192-77-8)

Safety Data

• Hazardous Substances Data: 102192-77-8(Hazardous Substances Data)

Upstream product

• 3587-60-8 Benzyloxymethyl chloride 
• 53924-05-3 7-chloro-1H-indole 
• 102147-52-4 N-benzyloxymethyl-3,4-dibromomaleimide 

Downstream Products

• 102147-53-5 1,11-dichloro-12,13-dihydro-6-[(phenylmethoxy)methyl]-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione 

Relevant articles and documents

A Stereoselective Synthesis of Indole-β-N-glycosides: An Application to the Synthesis of Rebeccamycin

Sodium salts of indoles have been found to open α-1,2-anhydrosugars with inversion yielding indole-β-N-glycosides.This methodology constitutes a concise route from glycals to the biologically active indole-N-glycosides.An application to the total synthesis of rebeccamycin is descibed.