| Weight | 356.506 g/mol |
|---|---|
| Formula | C23H32O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
16-Dehydropregnenolone acetate (979-02-2)
dehydropregnenolone acetate
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- Simplified Preparation of 16-Dehydropregnenolone Acetate (Synthesis, 1990)
- Stereoselective synthesis of (22R, 23R, 24S)-3-hydroxy-5-ene-22, 23-dihydroxy-24-methyl-cholestane : a brassinolide intermediate from 16-dehydropregnenolone acetate (Tetrahedron, 1994)
- A One-Pot Efficient Process for 16-Dehydropregnenolone Acetate (Organic Process Research & Development, 2003)
- Stereoselective syntheses of 20-epi cholanic acid derivatives from 16-dehydropregnenolone acetate (Tetrahedron, 2007)
- STEREOSELECTIVE SYNTHESIS OF A NEW HEXANOR(C23-C28)CASTASTERONE-20,22-ETHYL DIETHER FROM 16-DEHYDROPREGNENOLONE ACETATE AND ITS PLANT GROWTH PROMOTING ACTIVITY (Tetrahedron, 1997)
- Regio- and stereoselective thermal cycloaddition of -aryl-N-phenylnitrones to 16-dehydropregnenolone acetate: -facial selective addition of the minor rotamers of the nitrones (Tetrahedron Letters, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - dehydropregnenolone acetate
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SMILESCC(=O)C1=CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C
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InChIKeyMZWRIOUCMXPLKV-UHFFFAOYSA-N
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