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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H21NO3
Molecular Weight 299.3642
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HETEROCODEINE

SMILES

CO[C@H]1C=C[C@H]2[C@H]3CC4=CC=C(O)C5=C4[C@@]2(CCN3C)[C@H]1O5

InChI

InChIKey=FNAHUZTWOVOCTL-XSSYPUMDSA-N
InChI=1S/C18H21NO3/c1-19-8-7-18-11-4-6-14(21-2)17(18)22-16-13(20)5-3-10(15(16)18)9-12(11)19/h3-6,11-12,14,17,20H,7-9H2,1-2H3/t11-,12+,14-,17-,18-/m0/s1

HIDE SMILES / InChI

Molecular Formula C18H21NO3
Molecular Weight 299.3642
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:27:19 GMT 2025
Edited
by admin
on Mon Mar 31 23:27:19 GMT 2025
Record UNII
SBO5K94K8L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HETEROCODEINE
Common Name English
NSC-134601
Preferred Name English
MORPHINAN-3-OL, 7,8-DIDEHYDRO-4,5-EPOXY-6-METHOXY-17-METHYL-, (5.ALPHA.,6.ALPHA.)-
Systematic Name English
BRN-4268039
Common Name English
MORPHINE 6-METHYL ETHER
Common Name English
(5.ALPHA.,6.ALPHA.)-7,8-DIDEHYDRO-4,5-EPOXY-6-METHOXY-17-METHYLMORPHINAN-3-OL
Systematic Name English
O6-METHYLMORPHINE
Common Name English
Code System Code Type Description
NSC
134601
Created by admin on Mon Mar 31 23:27:19 GMT 2025 , Edited by admin on Mon Mar 31 23:27:19 GMT 2025
PRIMARY
WIKIPEDIA
Heterocodeine
Created by admin on Mon Mar 31 23:27:19 GMT 2025 , Edited by admin on Mon Mar 31 23:27:19 GMT 2025
PRIMARY
EPA CompTox
DTXSID40905126
Created by admin on Mon Mar 31 23:27:19 GMT 2025 , Edited by admin on Mon Mar 31 23:27:19 GMT 2025
PRIMARY
FDA UNII
SBO5K94K8L
Created by admin on Mon Mar 31 23:27:19 GMT 2025 , Edited by admin on Mon Mar 31 23:27:19 GMT 2025
PRIMARY
PUBCHEM
5462505
Created by admin on Mon Mar 31 23:27:19 GMT 2025 , Edited by admin on Mon Mar 31 23:27:19 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-356-3
Created by admin on Mon Mar 31 23:27:19 GMT 2025 , Edited by admin on Mon Mar 31 23:27:19 GMT 2025
PRIMARY
CAS
639-47-4
Created by admin on Mon Mar 31 23:27:19 GMT 2025 , Edited by admin on Mon Mar 31 23:27:19 GMT 2025
PRIMARY