160256-37-1

Basic information

• Product Name: 1H-Pyrrole-2,5-dione, 3-(1H-indol-3-yl)-1-[(phenylmethoxy)methyl]-4-[1-[[2-(trimethylsilyl)ethoxy ]methyl]-1H-indol-3-yl]-
• CAS NO: 160256-37-1
• Molecular Formula: C34H35N3O4Si
• Molecular Weight: 577.755
• Mol File: 160256-37-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-2,5-dione, 3-(1H-indol-3-yl)-1-[(phenylmethoxy)methyl]-4-[1-[[2-(trimethylsilyl)ethoxy ]methyl]-1H-indol-3-yl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-2,5-dione, 3-(1H-indol-3-yl)-1-[(phenylmethoxy)methyl]-4-[1-[[2-(trimethylsilyl)ethoxy ]methyl]-1H-indol-3-yl]-(160256-37-1)
• EPA Substance Registry System: 1H-Pyrrole-2,5-dione, 3-(1H-indol-3-yl)-1-[(phenylmethoxy)methyl]-4-[1-[[2-(trimethylsilyl)ethoxy ]methyl]-1H-indol-3-yl]-(160256-37-1)

Safety Data

• Hazardous Substances Data: 160256-37-1(Hazardous Substances Data)

Upstream product

• 160256-56-4 1-<(benzyloxy)methyl>-4-bromo-3,4-dihydro-3-<1H-indol-3-yl>-1H-pyrrole-2,5-dione 
• 160256-36-0 1-<(benzyloxy)methyl>-4-bromo-3,4-dihydro-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dione 
• 120-72-9 indole 
• 102147-52-4 N-benzyloxymethyl-3,4-dibromomaleimide 
• 76513-69-4 (2-trimethylethylsilylethoxy)methyl chloride 

Downstream Products

• 160256-55-3 C₂₇H₂₄N₄O₃ 
• 62996-74-1 staurosporine 
• 174290-90-5 1-<(benzyloxy)methyl>-3,4-dihydro-4-(<3-<<(benzyloxy)methyl>amino>-3-N,4-O-carbonyl-6-O-(4-methoxybenzyl)-α-D-altropyranosyl>-1H-indol-3-yl)-3-(1-<2-(trimethylsilyl)ethoxymethyl>-1H-indol-3-yl)-1H-pyrrole-2,5-dione 

Relevant articles and documents

Staurosporine and ent-staurosporine: The first total syntheses, prospects for a regioselective approach, and activity profiles

The total syntheses of staurosporine and ent-staurosporine have been achieved. Both glycosidic bonds were built from glycal precursors. The first was constructed by intermolecular coupling of an indole anion with a 1,2-anhydrosugar derived from an endo-glycal by direct epoxidation. The second bond was assembled from an exo-glycal by intramolecular iodoglycosylation.