56974-44-8

Basic information

• Product Name: 3,10-Perylenedione,4,9-dihydroxy-1,12-bis(2- hydroxypropyl)-2,6,7,11-tetramethoxy-,stereoisomer
• CAS NO: 56974-44-8
• Mol File: 56974-44-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3,10-Perylenedione,4,9-dihydroxy-1,12-bis(2- hydroxypropyl)-2,6,7,11-tetramethoxy-,stereoisomer (CAS DataBase Reference)
• NIST Chemistry Reference: 3,10-Perylenedione,4,9-dihydroxy-1,12-bis(2- hydroxypropyl)-2,6,7,11-tetramethoxy-,stereoisomer (56974-44-8)
• EPA Substance Registry System: 3,10-Perylenedione,4,9-dihydroxy-1,12-bis(2- hydroxypropyl)-2,6,7,11-tetramethoxy-,stereoisomer (56974-44-8)

Safety Data

• Hazardous Substances Data: 56974-44-8(Hazardous Substances Data)

Upstream product

• 133363-22-1 7,7'-Bis-((R)-2-hydroxy-propyl)-2,6,2',6'-tetramethoxy-4,4'-bis-methoxymethoxy-[1,1']binaphthalenyl-5,5'-diol 
• 133363-21-0 5,5'-Bis-benzyloxy-7,7'-bis-[(R)-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-2,6,2',6'-tetramethoxy-4,4'-bis-methoxymethoxy-[1,1']binaphthalenyl 
• 133363-19-6 [(S)-2-(4-Benzyloxy-8-bromo-3,7-dimethoxy-5-methoxymethoxy-naphthalen-2-yl)-1-methyl-ethoxy]-tert-butyl-diphenyl-silane 
• 133363-23-2 [(R)-2-(4-Benzyloxy-8-bromo-3,7-dimethoxy-5-methoxymethoxy-naphthalen-2-yl)-1-methyl-ethoxy]-tert-butyl-diphenyl-silane 
• 133363-18-5 1-Benzyloxy-5-bromo-3-[(S)-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-6-methoxy-8-methoxymethoxy-naphthalene-2-carbaldehyde 
• 133363-16-3 {1-Benzyloxy-3-[(S)-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-6-methoxy-8-methoxymethoxy-naphthalen-2-yl}-methanol 
• 133363-17-4 1-Benzyloxy-3-[(S)-2-(tert-butyl-diphenyl-silanyloxy)-propyl]-6-methoxy-8-methoxymethoxy-naphthalene-2-carbaldehyde 
• 133363-15-2 (S)-10-Hydroxy-7-methoxy-9-methoxymethoxy-3-methyl-3,4,4a,5-tetrahydro-benzo[g]isochromen-1-one 
• 133363-14-1 ethyl 4-methoxy-2-(methoxymethoxy)-6-methylbenzoate 
• 57749-86-7 ethyl 2,4-dimethoxy-6-methylbenzoate 
• 6110-36-7 ethyl everninate 
• 55018-89-8 2,4-dimethoxy-6-methylbenzoyl chloride 

Downstream Products

• 56974-44-8 isophleichrome 
• 123940-54-5 hypocrellin-B 

Relevant articles and documents

Optically active total synthesis of calphostin D

An optically active total synthesis of calphostin D (1a) through dimerization of the chiral o-naphthoquinone 6 has been accomplished. The mechanism of the dimerization has been shown to be an acid-catalyzed process.

Total synthesis of phleichrome, calphostin A, and calphostin D. Unusual stereoselective and stereospecific reactions in the synthesis of perylenequinones

This report describes the total synthesis of phleichrome, calphostin A and calphostin D - three protein kinase C inhibitory perylenequinones. The present route affords the targets in enantiomerically pure form and represents the first successful approach