
Aitheantas
Dydrogesterone Impurity 6
Gan liostú · C21H28O2
01Aitheantas
| Lazychem ID | LC-40467 |
|---|---|
| CAS RN | Gan liostú |
| PubChem CID | 53954141 |
| Molecular formula | C21H28O2 |
| Molecular weight | 312.4 g/mol |
| IUPAC name | (8S,9S,10R,13S,14S,17R)-17-acetyl-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one |
| InChIKey | JGMOKGBVKVMRFX-HXIANDDZSA-N |
02Struchtúr agus steiréicheimic

The parsed structure contains 4 rings, includes aliphatic carbon, has 6 defined stereocentres. These statements are calculated from the published structure string.
| Defined stereocentres | 6 |
|---|---|
| Ring count | 4 |
| Secondary amines | 0 |
| Tertiary amines | 0 |
| SMILES | CC(=O)[C@@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C=CC4=CC(=O)CC[C@]34C)C |
|---|---|
| InChI | Gan liostú |
03Stereochemistry
The published structure contains 6 defined and 0 unassigned tetrahedral stereocentres. The exact wedge and dash depiction is shown above.
Published same-connectivity configurations
4 recordsThese records have the same connectivity, molecular formula and protonation layer, but a different complete InChIKey stereochemical layer. Only separately structure-linked records are shown.


9beta,10alpha,17alpha-Pregna-4,6-diene-3,20-dione
CAS not listed
JGMOKGBVKVMRFX-POHNSKBLSA-N
6 defined, 0 unassigned centres

Dydrogesterone EP Impurity C
CAS 246038-13-1
JGMOKGBVKVMRFX-UHFFFAOYSA-N
0 defined, 6 unassigned centres

Scope: The mathematical 2^n value is only an upper bound. Symmetry and other stereogenic elements can change the number of distinct stereoisomers. A hypothetical configuration is not published as a compound record without a verified structure identity.
04Stádas san India
Exact-compound status is evaluated only against the published name and CAS number. Confirm the current official instrument before a regulatory decision.
05Ainmneacha agus gaolta
API agus máthairdhruga
Gan liostú
Ainmneacha agus gaolta
06Foinsí
- S01PubChem CID 53954141
Structure and machine-readable chemical identifiers.
