Methyl (5Z)-7-[(2R)-3,5-dihydroxy-2-{(1E)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]but-1-en-1-yl}cyclopentyl]hept-5-enoate, with CAS number 73275-76-0, is a complex organic compound characterized by its multi-functional structure, which includes multiple hydroxyl groups and a trifluoromethyl group. This compound features a heptenoate backbone, indicating the presence of a double bond within a seven-carbon chain, and it is further substituted with a cyclopentyl group that contributes to its stereochemistry. The presence of the trifluoromethyl group enhances its lipophilicity and may influence its biological activity. The hydroxyl groups suggest potential for hydrogen bonding, which can affect solubility and reactivity. This compound may be of interest in pharmaceutical chemistry due to its structural complexity and potential biological applications, particularly in the development of therapeutic agents. Its specific properties, such as melting point, boiling point, and solubility, would require empirical measurement or detailed literature reference for precise characterization.

methyl (5Z)-7-[(2R)-3,5-dihydroxy-2-{(1E)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]but-1-en-1-yl}cyclopentyl]hept-5-enoate

73275-76-0: Methyl (5Z)-7-[(2R)-3,5-dihydroxy-2-{(1E)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]but-1-en-1-yl}cyclopentyl]hept-5-enoate, with CAS number 73275-76-0, is a complex organic compound characterized by its multi-functional structure, which includes multiple hydroxyl groups and a trifluoromethyl group. This compound features a heptenoate backbone, indicating the presence of a double bond within a seven-carbon chain, and it is further substituted with a cyclopentyl group that contributes to its stereochemistry. The presence of the trifluoromethyl group enhances its lipophilicity and may influence its biological activity. The hydroxyl groups suggest potential for hydrogen bonding, which can affect solubility and reactivity. This compound may be of interest in pharmaceutical chemistry due to its structural complexity and potential biological applications, particularly in the development of therapeutic agents. Its specific properties, such as melting point, boiling point, and solubility, would require empirical measurement or detailed literature reference for precise characterization.

<p>Fluprostenol, a vet-approved luteolytic, has an isopropyl ester, travoprost, used as an eye pressure reducer. CAY10532 is its methyl ester form.</p>

CAS 73275-76-0

methyl (5Z)-7-[(2R)-3,5-dihydroxy-2-{(1E)-3-hydroxy-4-[3-(trifluoromethyl)phenoxy]but-1-en-1-yl}cyclopentyl]hept-5-enoate

Fluprostenol methyl ester

Ref: TM-T37813