56687-85-5 Usage
Description
(Z)-7-[2β-[(1E,3R)-3-Hydroxy-4-(3-chlorophenoxy)-1-butenyl]-3α,5α-dihydroxycyclopentane-1α-yl]-5-heptenoic acid methyl ester is a complex organic compound with a molecular structure characterized by a heptenoic acid backbone, a cyclopentane ring, and a chlorophenoxy substituent. This molecule exhibits a specific stereochemistry, with the Z configuration at the double bond and the 1E,3R configuration at the butenyl group. Its unique structure and functional groups may endow it with potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(Z)-7-[2β-[(1E,3R)-3-Hydroxy-4-(3-chlorophenoxy)-1-butenyl]-3α,5α-dihydroxycyclopentane-1α-yl]-5-heptenoic acid methyl ester is used as a pharmaceutical compound for its potential therapeutic properties. The molecule's unique structure and functional groups may allow it to interact with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (Z)-7-[2β-[(1E,3R)-3-Hydroxy-4-(3-chlorophenoxy)-1-butenyl]-3α,5α-dihydroxycyclopentane-1α-yl]-5-heptenoic acid methyl ester can be used as a starting material or a synthetic intermediate for the development of novel compounds with specific applications. Its unique structure may provide insights into the design and synthesis of new molecules with tailored properties.
Used in Material Science:
(Z)-7-[2β-[(1E,3R)-3-Hydroxy-4-(3-chlorophenoxy)-1-butenyl]-3α,5α-dihydroxycyclopentane-1α-yl]-5-heptenoic acid methyl ester may also find applications in material science, where its unique structure and functional groups could be exploited to create new materials with specific properties, such as improved mechanical strength, thermal stability, or chemical resistance.
Please note that the specific applications mentioned above are hypothetical and based on the general properties of the molecule. Further research and development would be required to validate these potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 56687-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,8 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56687-85:
(7*5)+(6*6)+(5*6)+(4*8)+(3*7)+(2*8)+(1*5)=175
175 % 10 = 5
So 56687-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C23H31ClO6/c1-29-23(28)10-5-3-2-4-9-19-20(22(27)14-21(19)26)12-11-17(25)15-30-18-8-6-7-16(24)13-18/h2,4,6-8,11-13,17,19-22,25-27H,3,5,9-10,14-15H2,1H3/b4-2-,12-11+/t17?,19?,20-,21?,22?/m1/s1
56687-85-5Relevant articles and documents
Side-modified 15-deoxy-Δ12,14-prostaglandin D2, precursor of corresponding PGJ2. Synthesis from cloprostenol and anticancer activity
Vostrikov, Nikolay S.,Lobko, Ilya F.,Spirikhin, Leonid V.,Vakhitova, Yulia V.,Pivnitsky, Kasimir K.,Miftakhov, Mansur S.
, p. 125 - 127 (2017)
The title compound, a possible precursor of metabolically stable corresponding PGJ2, was obtained from cloprostenol in seven steps. The compound demonstrated cytotoxicity against the HEK 293, Hep G2 and Jurkat cell lines.
A selective method for the preparation of aliphatic methyl esters in the presence of aromatic carboxylic acids
Rodriguez,Nomen,Spur,Godfroid
, p. 8563 - 8566 (2007/10/03)
2,2-Dimethoxypropane, methanol and a catalytic amount of HCl selectively esterify aliphatic carboxylic acids, in the presence of aromatic carboxylic acids, at room temperature and in high yields.
