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Details

Stereochemistry ACHIRAL
Molecular Formula C21H30O2
Molecular Weight 314.4617
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 4
Charge 0

SHOW SMILES / InChI
Structure of METHYL RETINOATE

SMILES

COC(=O)\C=C(C)\C=C\C=C(C)\C=C\C1=C(C)CCCC1(C)C

InChI

InChIKey=SREQLAJQLXPNMC-DXYSAURFSA-N
InChI=1S/C21H30O2/c1-16(9-7-10-17(2)15-20(22)23-6)12-13-19-18(3)11-8-14-21(19,4)5/h7,9-10,12-13,15H,8,11,14H2,1-6H3/b10-7+,13-12+,16-9+,17-15+

HIDE SMILES / InChI

Molecular Formula C21H30O2
Molecular Weight 314.4617
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 4
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:22:14 GMT 2025
Edited
by admin
on Mon Mar 31 19:22:14 GMT 2025
Record UNII
WS76I7L4S7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
RO 4-3781
Preferred Name English
METHYL RETINOATE
Common Name English
RETINOIC ACID, METHYL ESTER, ALL-TRANS-
Systematic Name English
ALL-TRANS-METHYL RETINOATE
Systematic Name English
METHYL ALL-TRANS-RETINOATE
Systematic Name English
VITAMIN A ACID METHYL ESTER
Systematic Name English
.BETA.-RETINOIC ACID METHYL ESTER
Systematic Name English
RETINOIC ACID, METHYL ESTER
Systematic Name English
ALL-TRANS-RETINOIC ACID METHYL ESTER
Systematic Name English
ALL-TRANS-VITAMIN A ACID METHYL ESTER
Systematic Name English
RETINOIC ACID METHYL ESTER
Common Name English
Code System Code Type Description
CAS
861043-70-1
Created by admin on Mon Mar 31 19:22:14 GMT 2025 , Edited by admin on Mon Mar 31 19:22:14 GMT 2025
SUPERSEDED
FDA UNII
WS76I7L4S7
Created by admin on Mon Mar 31 19:22:14 GMT 2025 , Edited by admin on Mon Mar 31 19:22:14 GMT 2025
PRIMARY
CAS
7432-07-7
Created by admin on Mon Mar 31 19:22:14 GMT 2025 , Edited by admin on Mon Mar 31 19:22:14 GMT 2025
SUPERSEDED
PUBCHEM
5378821
Created by admin on Mon Mar 31 19:22:14 GMT 2025 , Edited by admin on Mon Mar 31 19:22:14 GMT 2025
PRIMARY
EPA CompTox
DTXSID401316812
Created by admin on Mon Mar 31 19:22:14 GMT 2025 , Edited by admin on Mon Mar 31 19:22:14 GMT 2025
PRIMARY
CAS
339-16-2
Created by admin on Mon Mar 31 19:22:14 GMT 2025 , Edited by admin on Mon Mar 31 19:22:14 GMT 2025
PRIMARY