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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H23NO6
Molecular Weight 385.4104
Optical Activity ( - )
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,14-Diacetyloxymorphone

SMILES

[H][C@@]12OC3=C(OC(C)=O)C=CC4=C3[C@@]15CCN(C)[C@H](C4)[C@@]5(CCC2=O)OC(C)=O

InChI

InChIKey=OPPSZLCGCWIRIA-MBPVOVBZSA-N
InChI=1S/C21H23NO6/c1-11(23)26-15-5-4-13-10-16-21(28-12(2)24)7-6-14(25)19-20(21,8-9-22(16)3)17(13)18(15)27-19/h4-5,16,19H,6-10H2,1-3H3/t16-,19+,20+,21-/m1/s1

HIDE SMILES / InChI

Molecular Formula C21H23NO6
Molecular Weight 385.4104
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 16:59:23 UTC 2023
Edited
by admin
on Sat Dec 16 16:59:23 UTC 2023
Record UNII
EA7YNB52TR
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,14-Diacetyloxymorphone
Common Name English
Oxymorphone 3,14-diacetate
Common Name English
(5α)-3,14-Bis(acetyloxy)-4,5-epoxy-17-methylmorphinan-6-one
Systematic Name English
3,14-DIACETYLOXYMORPHONE, (-)-
Common Name English
[(4R,4aS,7aR,12bS)-4a-acetyloxy-3-methyl-7-oxo-2,4,5,6,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-9-yl]acetate
Systematic Name English
Morphinan-6-one, 3,14-bis(acetyloxy)-4,5-epoxy-17-methyl-, (5α)-
Systematic Name English
Diacetyloxymorphone
Common Name English
Code System Code Type Description
CAS
64643-76-1
Created by admin on Sat Dec 16 16:59:23 UTC 2023 , Edited by admin on Sat Dec 16 16:59:23 UTC 2023
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WIKIPEDIA
3,14-Diacetyloxymorphone
Created by admin on Sat Dec 16 16:59:23 UTC 2023 , Edited by admin on Sat Dec 16 16:59:23 UTC 2023
PRIMARY
EPA CompTox
DTXSID70983250
Created by admin on Sat Dec 16 16:59:23 UTC 2023 , Edited by admin on Sat Dec 16 16:59:23 UTC 2023
PRIMARY
PUBCHEM
56843406
Created by admin on Sat Dec 16 16:59:23 UTC 2023 , Edited by admin on Sat Dec 16 16:59:23 UTC 2023
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FDA UNII
EA7YNB52TR
Created by admin on Sat Dec 16 16:59:23 UTC 2023 , Edited by admin on Sat Dec 16 16:59:23 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> ENANTIOMER