313468-81-4

Basic information

• Product Name: C₃₉H₄₂O₇
• Synonyms: C₃₉H₄₂O₇
• CAS NO: 313468-81-4
• Molecular Weight: 622.758
• Mol File: 313468-81-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₉H₄₂O₇(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₉H₄₂O₇(313468-81-4)
• EPA Substance Registry System: C₃₉H₄₂O₇(313468-81-4)

Safety Data

• Hazardous Substances Data: 313468-81-4(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 313468-78-9 3-benzyloxy-13α-hydroxymethyl-14β-(prop-2-en-yl)-des-D-estra-1,3,5(10)-triene 
• 313468-79-0 (4aS,4bR,10bS,12aS)-8-Benzyloxy-3-iodomethyl-12a-methyl-3,4,4a,4b,5,6,10b,11,12,12a-decahydro-1H-2-oxa-chrysene 
• 80370-42-9 ethyl 2-formyl-3-oxopropanoate 
• 313468-80-3 (4aS,4bR,10bS,12aS)-8-Benzyloxy-12a-methyl-3-methylene-3,4,4a,4b,5,6,10b,11,12,12a-decahydro-1H-2-oxa-chrysene 

Downstream Products

• 313468-83-6 C₃₀H₃₈O₅ 
• 313468-82-5 C₃₀H₃₆O₅ 

Relevant articles and documents

A novel approach in drug discovery: Synthesis of estrone-talaromycin natural product hybrids

Hetero-Diels - Alder reaction of the steroidal exocyclic enol ethers 14 and 15, obtained from the secoestrones 8 and 9 by reduction, iodoetherification, and elimination, with ethyl O-benzoyldiformylacetate (16) leads to the spiroacetals 17 and 18 as a mixture of four diastereomers. Reduction of the major diastereomers 17a and 18 a with DIBAH and subsequent hydrogenation yields the novel natural product hybrids 21, 23, 24, and 25, which possess the structural features of the steroid estrone (7) and the mycotoxin talaromycin 6.