34603-80-0

Basic information

• Product Name: R 46500
• CAS NO: 34603-80-0
• Mol File: 34603-80-0.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: R 46500(CAS DataBase Reference)
• NIST Chemistry Reference: R 46500(34603-80-0)
• EPA Substance Registry System: R 46500(34603-80-0)

Safety Data

• Hazardous Substances Data: 34603-80-0(Hazardous Substances Data)

Upstream product

• 50999-74-1 2-(6-Oxiranyl-hexyl)-cyclopent-2-enone 
• 23472-43-7 7-[(1S,2R)-2-((E)-(R)-3-Acetoxy-oct-1-enyl)-5-oxo-cyclopentyl]-heptanoic acid methyl ester 
• 57378-32-2 15α-hydroxy-11-deoxyprostaglandin-E₁ ethyl ester 
• 20721-87-3 (+/-)-15-epi-11-deoxy PGE₁ methyl ester 
• 52477-97-1 2-(7-butoxycarbonylhexyl)-2-cyclopenten-1-one 
• 39647-93-3 (S)-(E)-(+)-1-Iodo-1-octen-3-ol 
• 5239-43-0 7-(5-oxo-1-cyclopenten-1-yl)heptanoic acid 
• 32556-71-1 1-octyn-3-ol 
• 42542-00-7 (S)-3-(1-ethoxy-ethoxy)-1t-iodo-oct-1-ene 
• 34546-57-1 2-(6-methoxycarbonylhexyl)cyclopent-2-en-1-one 
• 39198-04-4 (E)-1-chloro-oct-1-en-3-one 
• 52487-91-9 1-iodo-3-(p-anisyldiphenylmethoxy)-trans-1-octene 
• 39178-64-8 (E)-1-iodo-1-octen-3-one 
• 39178-65-9 (E)-1-iodooct-1-en-3-ol 

Downstream Products

• 5239-90-7 11-deoxy-PGF_1α 
• 5239-90-7 11-deoxy PGF_1β 
• 21269-27-2 15α-hydroxy-11-deoxy-8β,12β-prostaglandin-E₁ 
• 5239-90-7 (+/-)-15-epi-11-deoxyprostaglandin F_1α 
• 5239-90-7 (+/-)-15-epi-11-deoxyprostaglandin F_1β 
• 24341-38-6 (+/-)-15-epi-13.14-Dihydro-11-deoxy-PGE(1) 
• 24341-38-6 (+/-)-13.14-Dihydro-11-deoxy-PGE(1) 

Relevant articles and documents

SYNTHESIS AND PHARMACOLOGICAL PROPERTIES OF &α-HOMOANALOGS OF 11-DESOXYPROSTAGLANDIN E1

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CONDENSATION OF ALLYL SULFOXIDES WITH CYCLOPENTENONES IN THE SYNTHESIS OF PROSTAGLANDINS. STEREOSPECIFIC TOTAL SYNTHESIS OF 11-DEOXYPROSTAGLANDIN-E1

The reactions of the vinyl sulfoxide group in the products from the addition of the carbanions of allyl sulfoxides to cyclopentenones were investigated.The α-alkylated vinyl sulfoxide is converted

Prostaglandins and congeners. 20. Synthesis of prostaglandins via conjugate addition of lithium trans-1-alkenyltrialkylalanate reagents. A novel reagent for conjugate 1,4-additions

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