U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C22H30O4
Molecular Weight 358.4712
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CANNABICHROMENIC ACID, (±)-

SMILES

CCCCCC1=C(C(O)=O)C(O)=C2C=CC(C)(CCC=C(C)C)OC2=C1

InChI

InChIKey=HRHJHXJQMNWQTF-UHFFFAOYSA-N
InChI=1S/C22H30O4/c1-5-6-7-10-16-14-18-17(20(23)19(16)21(24)25)11-13-22(4,26-18)12-8-9-15(2)3/h9,11,13-14,23H,5-8,10,12H2,1-4H3,(H,24,25)

HIDE SMILES / InChI

Molecular Formula C22H30O4
Molecular Weight 358.4712
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 18:42:40 UTC 2023
Edited
by admin
on Sat Dec 16 18:42:40 UTC 2023
Record UNII
GHH6KX8TQS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CANNABICHROMENIC ACID, (±)-
Common Name English
(±)-CANNABICHROMENIC ACID A
Common Name English
5-HYDROXY-2-METHYL-2-(4-METHYL-3-PENTEN-1-YL)-7-PENTYL-2H-1-BENZOPYRAN-6-CARBOXYLIC ACID
Systematic Name English
2H-1-BENZOPYRAN-6-CARBOXYLIC ACID, 5-HYDROXY-2-METHYL-2-(4-METHYL-3-PENTEN-1-YL)-7-PENTYL-
Systematic Name English
(±)-CANNABICHROMENIC ACID
Common Name English
Code System Code Type Description
WIKIPEDIA
Cannabichromenic acid
Created by admin on Sat Dec 16 18:42:40 UTC 2023 , Edited by admin on Sat Dec 16 18:42:40 UTC 2023
PRIMARY
PUBCHEM
3084339
Created by admin on Sat Dec 16 18:42:40 UTC 2023 , Edited by admin on Sat Dec 16 18:42:40 UTC 2023
PRIMARY
FDA UNII
GHH6KX8TQS
Created by admin on Sat Dec 16 18:42:40 UTC 2023 , Edited by admin on Sat Dec 16 18:42:40 UTC 2023
PRIMARY
CAS
185505-15-1
Created by admin on Sat Dec 16 18:42:40 UTC 2023 , Edited by admin on Sat Dec 16 18:42:40 UTC 2023
PRIMARY
EPA CompTox
DTXSID301336859
Created by admin on Sat Dec 16 18:42:40 UTC 2023 , Edited by admin on Sat Dec 16 18:42:40 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE