126935-09-9

Basic information

• Product Name: (9aS,10S)-5a-Hydroxy-10-(4-methoxy-phenyl)-5a,6,7,8,9a,10-hexahydro-1,3,5-trioxa-cyclopenta[b]anthracen-9-one
• CAS NO: 126935-09-9
• Molecular Weight: 368.386
• Mol File: 126935-09-9.mol

Chemical Properties

• CAS DataBase Reference: (9aS,10S)-5a-Hydroxy-10-(4-methoxy-phenyl)-5a,6,7,8,9a,10-hexahydro-1,3,5-trioxa-cyclopenta[b]anthracen-9-one(CAS DataBase Reference)
• NIST Chemistry Reference: (9aS,10S)-5a-Hydroxy-10-(4-methoxy-phenyl)-5a,6,7,8,9a,10-hexahydro-1,3,5-trioxa-cyclopenta[b]anthracen-9-one(126935-09-9)
• EPA Substance Registry System: (9aS,10S)-5a-Hydroxy-10-(4-methoxy-phenyl)-5a,6,7,8,9a,10-hexahydro-1,3,5-trioxa-cyclopenta[b]anthracen-9-one(126935-09-9)

Safety Data

• Hazardous Substances Data: 126935-09-9(Hazardous Substances Data)

Upstream product

• 504-02-9 1,3-cylohexanedione 
• 116385-13-8 6-[(4-Methoxy-phenyl)-pyrrolidin-1-yl-methyl]-benzo[1,3]dioxol-5-ol 

Downstream Products

• 126935-10-2 10-(4-Methoxy-phenyl)-6,7,8,10-tetrahydro-1,3,5-trioxa-cyclopenta[b]anthracen-9-one 

Relevant articles and documents

Synthesis of new benzopyrans related to podophyllotoxin

Mannich bases of types 1 or 8, which are readily synthesized by condensation of 3,4-methylenedioxyphenol with aromatic aldehydes and pyrrolidine or piperazine, react with cyclic and acyclic β-diketones to yield benzopyrans. These benzopyrans are structurally similar to podophyllotoxin and like this drug some of the benzopyrans show in vivo anti-leukemic action in mice.