
Azonosítás
H40087
CAS 1429504-48-2 · C31H30N2O8
01Azonosítás
| Lazychem ID | LC-11975 |
|---|---|
| CAS RN | 1429504-48-2 |
| PubChem CID | 102205728 |
| Molecular formula | C31H30N2O8 |
| Molecular weight | 558.59 g/mol |
| IUPAC name | (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-(N-(tert-butoxycarbonyl)formamido)phenyl)-4-oxobutanoic acid |
| InChIKey | DYKDQJGTAYUDIW-VWLOTQADSA-N |
02Szerkezet és sztereokémia

| SMILES | CC(C)(C)OC(=O)N(C=O)C1=CC=CC=C1C(=O)C[C@@H](C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24 |
|---|---|
| InChI | Nincs megadva |
03Stereochemistry
The published structure contains 1 defined and 0 unassigned tetrahedral stereocentre. The exact wedge and dash depiction is shown above.
Published same-connectivity configurations
1 recordThese records have the same connectivity, molecular formula and protonation layer, but a different complete InChIKey stereochemical layer. Only separately structure-linked records are shown.

No additional structure-linked configuration with the same connectivity is currently present in the LazyChem dataset.
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.
04Indiai státusz
Exact-compound status is evaluated only against the published name and CAS number. Confirm the current official instrument before a regulatory decision.
05Nevek és kapcsolatok
API és anyavegyület
Daptomycin
Szennyezők és rokon vegyületekNevek és kapcsolatok
- Daptomycin Impurity 27
- (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-(N-(tert-butoxycarbonyl)formamido)phenyl)-4-oxobutanoic acid
06Források
- S01PubChem CID 102205728
Structure and machine-readable chemical identifiers.
