- Flugestone 17-acetate
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- $0.00 / 1kg
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2026-02-13
- CAS:2529-45-5
- Min. Order: 1kg
- Purity: 97%-103%
- Supply Ability: 100kg
- Fluorogestone acetate
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- $35.00 / 2mg
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2026-01-26
- CAS:2529-45-5
- Min. Order:
- Purity: 99.78%
- Supply Ability: 10g
- Flugestone 17-acetate
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- $0.00 / 1KG
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2025-09-23
- CAS:2529-45-5
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: 2000
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| | Flugestone 17-acetate Basic information |
| Product Name: | Flugestone 17-acetate | | Synonyms: | 4-PREGNEN-9-ALPHA-FLUORO-11-BETA, 17-DIOL-3,20-DIONE ACETATE;FLUOROGESTONE ACETATE;FLUGESTONE ACETATE;17-(acetyloxy)-9-fluoro-11-hydroxy-20-dion(11-beta)-pregn-4-ene-;20-dione,9-fluoro-11-beta,17-dihydroxy-pregn-4-ene-17-acetate;cronolone;(11β)-17-(Acetyloxy)-9-fluoro-11-hydroxy-pregn-4-ene-3,20-dione;17α-Acetoxy-9α-fluoro-11β-hydroxy-pregn-4-ene-3,20-dione | | CAS: | 2529-45-5 | | MF: | C23H31FO5 | | MW: | 406.49 | | EINECS: | 219-776-9 | | Product Categories: | Pharmaceuticals;Steroids;Intermediates & Fine Chemicals;2529-45-5 | | Mol File: | 2529-45-5.mol |  |
| | Flugestone 17-acetate Chemical Properties |
| Melting point | 266-269° | | alpha | D +77.6° (in chloroform) | | Boiling point | 526.7±50.0 °C(Predicted) | | density | 1.24±0.1 g/cm3(Predicted) | | storage temp. | Refrigerator | | solubility | Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Sparingly) | | pka | 13.09±0.70(Predicted) | | form | Solid | | color | White to Off-White | | Water Solubility | Water: Insoluble | | InChIKey | JKQQZJHNUVDHKP-RBVORTGHNA-N | | SMILES | C[C@]12C[C@H](O)[C@@]3([C@]4(CCC(=O)C=C4CC[C@@]3([H])[C@]1([H])CC[C@@]2(C(=O)C)OC(=O)C)C)F |&1:1,3,5,6,15,17,21,r| | | CAS DataBase Reference | 2529-45-5 |
| | Flugestone 17-acetate Usage And Synthesis |
| Uses | Flugestone 17-acetate is a synthetic progesterone, used to induce oestrus synchronisation in goats and sheep. | | Definition | ChEBI: Flurogestone acetate is a corticosteroid hormone. | | Synthesis | The method for the preparation of fluoroprogesterone acetate is based on 9a-fluorohydrocortisone, which is dissolved in an organic solvent and reacted with chloroyl chloride in the presence of an acid-binding agent to obtain the 9a-fluorohydrocortisone-21-O-esterified substance; then this esterified substance is reacted with sodium iodide and sulfur-containing reducing agent in an organic solvent to de-esterify and synthesize fluoroprogesterone; and finally, the fluoroprogesterone is reacted with acetochlorine or acetic anhydride in an organic solvent to synthesize fluoroprogesterone. Finally, the fluoroprogesterone is reacted with acetyl chloride or acetic anhydride in organic solvent to synthesize fluoroprogesterone acetate. |
| | Flugestone 17-acetate Preparation Products And Raw materials |
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