CAS 55028-72-3
:5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-chlorophenoxy)-3-hydroxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-, sodium salt (1:1), (5Z)-rel-
Description:
5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-chlorophenoxy)-3-hydroxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-, sodium salt (1:1), (5Z)-rel- is a complex organic compound characterized by its unique structure, which includes a heptenoic acid backbone and a cyclopentyl moiety with multiple hydroxyl groups. This compound features a sodium salt form, indicating it is likely soluble in water and may exhibit ionic properties. The presence of a chlorophenoxy group suggests potential biological activity, possibly as a herbicide or pharmaceutical agent. The stereochemistry indicated by the (1R,2R,3R,5S) and (5Z)- designations implies specific spatial arrangements of atoms, which can significantly influence the compound's reactivity and interactions with biological systems. Overall, this compound's characteristics suggest it may have applications in various fields, including agriculture and medicinal chemistry, although specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.
Formula:C22H29ClO6·Na
InChI:InChI=1/C22H29ClO6.Na/c23-15-6-5-7-17(12-15)29-14-16(24)10-11-19-18(20(25)13-21(19)26)8-3-1-2-4-9-22(27)28;/h1,3,5-7,10-12,16,18-21,24-26H,2,4,8-9,13-14H2,(H,27,28);/b3-1-,11-10+;/t16-,18-,19-,20+,21-;/s2
InChI key:InChIKey=QXXAYZMVSNAWKP-HIFRLICANA-N
SMILES:C(/C=C\CCCC(O)=O)[C@H]1[C@H](/C=C/[C@@H](COC2=CC(Cl)=CC=C2)O)[C@@H](O)C[C@H]1O.[Na]
Synonyms:- (+/-)-Cloprostenol
- (5Z)-7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-Chlorophenoxy)-3-hydroxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-5-heptenoic acid sodium salt
- (S)-Cloprostenol Sodium
- 5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-chlorophenoxy)-3-hydroxy-1-buten-1-yl]-3,5-dihydroxycyclopentyl]-, sodium salt (1:1), (5Z)-rel-
- 5-Heptenoic acid, 7-[(1R,2R,3R,5S)-2-[(1E,3R)-4-(3-chlorophenoxy)-3-hydroxy-1-butenyl]-3,5-dihydroxycyclopentyl]-, monosodium salt, (5Z)-rel-
- 5-Heptenoic acid, 7-[2-[4-(3-chlorophenoxy)-3-hydroxy-1-butenyl]-3,5-dihydroxycyclopentyl]-, monosodium salt, [1α(Z),2β(1E,3R*),3α,5α]-
- Ciosin
- Cloprostenol sodium salt
- D-Cloprostenol sodium
- DL-Cloprostenol Sodium
- Estrumat
- Estrumate
- Ici 80996
- Planate
- Vetmate
- See more synonyms
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Found 9 products.
Cloprostenol sodium
CAS:Cloprostenol sodiumFormula:(C22H28ClNaO6)Color and Shape:White To Off-WhiteMolecular weight:446.14721Cloprostenol Sodium
CAS:Prostaglandins, thromboxanes and leukotrienes, their derivatives and structural analoguesFormula:C22H28ClNaO6Color and Shape:White Off-White PowderMolecular weight:446.14721(+/-)-Cloprostenol sodium salt hydrate
CAS:Formula:C22H28ClNaO6·xH2OPurity:≥ 98%Color and Shape:White to off-white powderMolecular weight:446.90 (anhydrous)DL-Cloprostenol Sodium Salt
CAS:Formula:C22H28ClO6·NaColor and Shape:White To Off-White SolidMolecular weight:423.92 22.99Cloprostenol sodium salt
CAS:<p>Cloprostenol sodium salt (ICI 80996 sodium salt) is a synthetic prostaglandin analogue, an agonist at the PGF2α receptor, with luteolytic properties.</p>Formula:C22H28ClNaO6Purity:97.17% - 98.47%Color and Shape:White To Almost White Hygroscopic PowderMolecular weight:446.9(5Z)-rel-Cloprostenol Sodium
CAS:<p>Applications (5Z)-rel-Cloprostenol Sodium Salt is the d-enantiomer of Cloprostenol (C587300), an aryl-oxymethyl analog of prostaglandin F2α.<br>References Gumen, A., et al.: J. Animal. Sci., 56, 279 (2011); Leterlier, C.A., et al.: Reproduct. Domestic. Animals., 46, 481 (2011); Martins, J.P.N., et al.: J. Diary. Sci., 94, 2815 (2011);<br></p>Formula:C22H28ClO6·NaColor and Shape:White To Off-WhiteMolecular weight:446.90Cloprostenol sodium
CAS:<p>Cloprostenol sodium is a prostaglandin analogue that is used in veterinary medicine. It is administered intravenously to induce ovulation, improve estrus and fertility, or control luteal function in cows. Cloprostenol sodium has been shown to have a positive effect on the ovulatory process by stimulating the release of endogenous progesterone and estradiol benzoate from the follicle cells. This drug also increases luteal activity by increasing the production of progesterone and inhibiting its metabolism. Cloprostenol sodium has been shown to be effective in inducing ovulation in pregnant women who do not respond to clomiphene citrate (CC) alone. Cloprostenol sodium can also be used for induction of labour in pregnant women with an uncomplicated pregnancy at term, where it is given intravenously or intramuscularly, but intravaginally or orally are not recommended.</p>Formula:C22H28ClNaO6Purity:Min. 95%Color and Shape:White PowderMolecular weight:446.9 g/mol









