Identità

(E)-17-Deoxyaldehyde Derivative

CAS 105562-12-7 · C21H28O4

01Identità

Lazychem IDLC-00500
CAS RN105562-12-7
PubChem CID14261066
Molecular formulaC21H28O4
Molecular weight344.45 g/mol
IUPAC name(11b,17E)-11,20-dihydroxy-3-oxo-pregna-4,17(20)-dien-21-al
InChIKeyJVIOAMIJLAYISK-GTILSLFGSA-N

02Struttura u stereokimika

2D structurePubChem CID 14261066
Two-dimensional chemical structure of (E)-17-Deoxyaldehyde Derivative, CAS 105562-12-7
Two-dimensional structure for the PubChem identity linked to this record. Confirm the identifiers before analytical use.
SMILESC[C@]12CCC(=O)C=C1CC[C@@H]3[C@@H]2[C@H](C[C@]\4([C@H]3CC/C4=C(/C=O)\O)C)O
InChIMhux elenkat

03Stereochemistry

The published structure contains 6 defined and 0 unassigned tetrahedral stereocentres. The exact wedge and dash depiction is shown above.

Defined centres6Structure assigned
Unassigned centres0Structure unspecified
Assignment statusFully assignedExact published identity
Tetrahedral upper bound≤ 64Before symmetry reduction

Published same-connectivity configurations

2 records

These records have the same connectivity, molecular formula and protonation layer, but a different complete InChIKey stereochemical layer. Only separately structure-linked records are shown.

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.

04Status fl-Indja

Exact-compound status is evaluated only against the published name and CAS number. Confirm the current official instrument before a regulatory decision.

05Ismijiet u relazzjonijiet

API u mediċina prinċipali

Hydrocortisone

Impuritajiet u komposti relatati

Ismijiet u relazzjonijiet

  • (11beta,17E)-11,20-dihydroxy-3-oxo-pregna-4,17(20)-dien-21-al
  • Hydrocortisone (E)-17-Deoxyaldehyde Derivative

Impuritajiet u komposti relatati

06Sorsi