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| 16a,17a-Epoxyprogesterone Basic information |
| Product Name: | 16a,17a-Epoxyprogesterone | | Synonyms: | 16,17-Epoxypregn-4-ene-3,20-dione;16-alpha,17-epoxy-pregn-4-ene-20-dione;16-alpha,17-epoxypregn-4-ene-3,20-dione;16,17-EPOXYPROGESTERONE;16,17-ALPHA-EPOXYPROGESTERONE;16a,17a-epoxy-4-pregnen-3,20-dione;17-epoxy-20-dion(16-alpha)-pregn-4-ene-16;W-oxide | | CAS: | 1097-51-4 | | MF: | C21H28O3 | | MW: | 328.45 | | EINECS: | 214-147-5 | | Product Categories: | Biochemistry;Steroids;Steroids (Others) | | Mol File: | 1097-51-4.mol |
| 16a,17a-Epoxyprogesterone Chemical Properties |
| Melting point | 200C | | Boiling point | 466.9±45.0 °C(Predicted) | | density | 1.18±0.1 g/cm3(Predicted) | | refractive index | 168 ° (C=1, CHCl3) | | storage temp. | Sealed in dry,Store in freezer, under -20°C | | solubility | Chloroform, Methanol | | form | Solid | | color | Off-White | | CAS DataBase Reference | 1097-51-4(CAS DataBase Reference) |
| WGK Germany | 3 | | RTECS | TU5022000 |
| 16a,17a-Epoxyprogesterone Usage And Synthesis |
| Uses | 16α,17α-Epoxyprogesterone is hydrolyzed by Rhizopus nigricans for the synthesis of many steroidal drugs. |
| 16a,17a-Epoxyprogesterone Preparation Products And Raw materials |
| Raw materials | Cyclohexanone-->Aluminium isopropoxide-->Diosgenin | | Preparation Products | Cortisone acetate-->CORTISONE-->21-Iodo-16-methylpregna-1,4,9(11)-trien-17-ol-3,20-dione-->17-hydroxy-6-methylenepregn-4-ene-3,20-dione 17-acetate-->Megestrol acetate-->16-Methylpregna-1,4,9(11)-trien-17-ol-3,20-dione-->3,20-Dioxopregn-4-en-17-beta-yl acetate-->17-Hydroxy-21-iodoprogesterone-->16-Bromo-17-hydroxypregn-4-en-3,20-dione-->3,17-DIHYDROXY-PREGNA-3,5-DIEN-20-ONE DIACETATE-->3-ethoxy-17-hydroxypregna-3,5-dien-20-one 17-acetate |
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