206555-98-8

Basic information

• Product Name: Cloprostenol
• Synonyms: (5Z)-rel-7-[(1R,2R,3R,5S)-2-[(1E,3S)-4-(3-Chlorophenoxy)-3-hydroxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-5-heptenoic Acid
• CAS NO: 206555-98-8
• Molecular Formula: C₂₂H₂₉ClO₆
• Molecular Weight: 386.65354
• Product Categories: Chiral Reagents;Intermediates & Fine Chemicals;Pharmaceuticals;Chiral Reagents, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 206555-98-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 628.0±55.0 °C(Predicted)
• Appearance: /
• Density: 1.321±0.06 g/cm3(Predicted)
• Storage Temp.: -20°C Freezer, Under Inert Atmosphere
• PKA: 4.76±0.10(Predicted)
• CAS DataBase Reference: Cloprostenol(CAS DataBase Reference)
• NIST Chemistry Reference: Cloprostenol(206555-98-8)
• EPA Substance Registry System: Cloprostenol(206555-98-8)

Safety Data

• Hazardous Substances Data: 206555-98-8(Hazardous Substances Data)

Usage

Chemical Properties

Yellow Oil

Uses

Aryl-oxymethyl analog of prostaglandin F2α.

Upstream product

• 52267-81-9 (3aR,4R,5R,6aS)-4-[(E)-4-(3-Chloro-phenoxy)-3-hydroxy-but-1-enyl]-5-hydroxy-hexahydro-cyclopenta[b]furan-2-one 
• 130325-32-5 Formic acid (3aR,4S,5R,6aS)-4-formyloxymethyl-2-oxo-hexahydro-cyclopenta[b]furan-5-yl ester 
• 53872-62-1 Cloprostenol 
• 62961-72-2 Corey aldehyde 
• 26054-46-6 (-)-(1S,5R)-2-oxabicyclo[3.3.0]oct-6-en-3-one 
• 32233-40-2 (3aR,4S,5R,6aS)-5-hydroxy-4-(hydroxymethyl)hexahydro-2H-cyclopenta[b]furan-2-one 
• 40665-92-7 cloprostenol 
• 41723-91-5 4-carboxybutyliden triphenylphosphorane sodium 
• 89560-44-1 (3aR,4R,5R,6aS)-4-[(E)-4-(3-Chloro-phenoxy)-3-hydroxy-but-1-enyl]-hexahydro-cyclopenta[b]furan-2,5-diol 

Relevant articles and documents

The tetrahydropyranyl-protected mandelic acid: A novel versatile chiral derivatising agent

A simple synthesis of (2R)-2-phenyl-2-[(2S)-tetrahydro-2- pyranyloxy]ethanoic acid, a versatile chiral derivatising agent (CDA), is proposed. The derivatisation of secondary alcohols aimed at the absolute configurational assignment, determination of enantiomeric purity as well as semipreparative resolution is described.