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| | Pregn-4-ene-3,20-dione,21-(acetyloxy)-6-fluoro-11,17-dihydroxy-, (6a,11b)- (9CI) Basic information |
| Product Name: | Pregn-4-ene-3,20-dione,21-(acetyloxy)-6-fluoro-11,17-dihydroxy-, (6a,11b)- (9CI) | | Synonyms: | Pregn-4-ene-3,20-dione,21-(acetyloxy)-6-fluoro-11,17-dihydroxy-, (6a,11b)- (9CI);6alpha-fluoro-17-hydroxycorticosterone 21-acetate;Pregn-4-ene-3,20-dione, 21-(acetyloxy)-6-fluoro-11,17-dihydroxy-, (6α,11β)- | | CAS: | 1058-55-5 | | MF: | C23H31FO6 | | MW: | 422.49 | | EINECS: | | | Product Categories: | | | Mol File: | 1058-55-5.mol |  |
| | Pregn-4-ene-3,20-dione,21-(acetyloxy)-6-fluoro-11,17-dihydroxy-, (6a,11b)- (9CI) Chemical Properties |
| Melting point | 203-210 °C | | Boiling point | 578.3±50.0 °C(Predicted) | | density | 1.30±0.1 g/cm3(Predicted) | | pka | 12.27±0.70(Predicted) |
| | Pregn-4-ene-3,20-dione,21-(acetyloxy)-6-fluoro-11,17-dihydroxy-, (6a,11b)- (9CI) Usage And Synthesis |
| Definition | ChEBI: 6alpha-fluoro-17-hydroxycorticosterone 21-acetate is a steroid ester that is pregn-4-en-21-yl acetate substituted by oxo groups at positions 3 and 20, hydroxy groups at positions 11 and 17 and a fluoro group at position 6. It is a fluorinated steroid, a steroid ester, an acetate ester, an 11beta-hydroxy steroid, a 17alpha-hydroxy steroid, a 3-oxo-Delta(4) steroid, a 20-oxo steroid and a tertiary alpha-hydroxy ketone. It derives from a hydride of a pregnane. |
| | Pregn-4-ene-3,20-dione,21-(acetyloxy)-6-fluoro-11,17-dihydroxy-, (6a,11b)- (9CI) Preparation Products And Raw materials |
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