69381-94-8

Basic information

• Product Name: fenprostalene
• Synonyms: fenprostalene;Porcilene;RS-84043;(4S)-rel-7-[(1R,2R,3R,5S)-3,5-Dihydroxy-2-[(1E,3R)-3-hydroxy-4-phenoxy-1-buten-1-yl]cyclopentyl]-4,5-heptadienoic Acid Methyl Ester;[1α(S*),2β(1E,3R*),3α,5α]-7-[3,5- Dihydroxy-2-(3-hydroxy-4-phenoxy-1-butenyl)cyclopentyl]-4,5-heptadienoic Acid Methyl Ester;Bovilene;4,5-Heptadienoic acid,7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3R)-3-hydroxy-4-phenoxy-1-buten-1-yl]cyclopentyl]-,Methyl ester, (4S)-rel-
• CAS NO: 69381-94-8
• Molecular Formula: C₂₃H₃₀O₆
• Molecular Weight: 402.484
• EINECS: 273-982-3
• Product Categories: Aromatics;Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 69381-94-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 553.9 ºC at 760 mmHg
• Flash Point: 185.2 ºC
• Appearance: /
• Density: 1.206 g/cm³
• Vapor Pressure: 4.21E-13mmHg at 25°C
• Refractive Index: 1.594
• PKA: 13.57±0.20(Predicted)
• CAS DataBase Reference: fenprostalene(CAS DataBase Reference)
• NIST Chemistry Reference: fenprostalene(69381-94-8)
• EPA Substance Registry System: fenprostalene(69381-94-8)

Safety Data

• Hazardous Substances Data: 69381-94-8(Hazardous Substances Data)

Usage

Uses

Synthetic analog of Prostaglandin F2α, related structurally to Prostalene. Luteolytic.

Brand name

Synchrocept B [Veterinary] (Syntex).

InChI:InChI=1/C23H30O6/c1-28-23(27)12-8-3-2-7-11-19-20(22(26)15-21(19)25)14-13-17(24)16-29-18-9-5-4-6-10-18/h3-7,9-10,13-14,17,19-22,24-26H,8,11-12,15-16H2,1H3/b14-13+/t2?,17-,19-,20?,21+,22-/m1/s1

Relevant articles and documents

16-Phenoxy and 16-substituted phenoxy-prostatrienoic acid derivatives

Novel racemic and 8R-antimeric 16-phenoxy- and 16-(o, m or p)-substituted phenoxy derivatives of 9α, 11α,15-trihydroxy-17,18,19,20-tetranorprosta-4,5,13-trans-trienoic acids, which may be further substituted at C-15 by a methyl or ethyl group, the pharmaceutically acceptable, non-toxic lower alkyl esters and salts thereof and processes for the production of such compounds. dl 9α,11α,15α-trihydroxy-16-m-trifluoromethylphenoxy-17,18,19,20-tetranorprosta-4,5,13-trans-trienoic acid and dl 9α,11α,15 -trihydroxy-15 -methyl-16-m-trifluoromethylphenoxy-17,18,19,20-tetranorprosta-4,5,13-trans-trienoic acid are representative compounds of the class. These compounds possess prostaglandin-like activities and thus are useful in the treatment of mammals where prostaglandins are indicated. They are particularly useful as luteolytic agents in female mammals.