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Details

Stereochemistry RACEMIC
Molecular Formula C10H16O4
Molecular Weight 200.2316
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CAMPHORIC ACID

SMILES

CC1(C)[C@H](CC[C@@]1(C)C(O)=O)C(O)=O

InChI

InChIKey=LSPHULWDVZXLIL-LDWIPMOCSA-N
InChI=1S/C10H16O4/c1-9(2)6(7(11)12)4-5-10(9,3)8(13)14/h6H,4-5H2,1-3H3,(H,11,12)(H,13,14)/t6-,10+/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H16O4
Molecular Weight 200.2316
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:17:16 UTC 2023
Edited
by admin
on Fri Dec 15 16:17:16 UTC 2023
Record UNII
32K0C7JGCJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CAMPHORIC ACID
MI   WHO-DD  
Common Name English
DL-CAMPHORIC ACID
Common Name English
Camphoric acid [WHO-DD]
Common Name English
1,2,2-TRIMETHYL-1,3-CYCLOPENTANECARBOXYLIC ACID
Common Name English
CAMPHORIC ACID [MI]
Common Name English
CAMPHORIC ACID, DL-
Common Name English
NSC-60219
Code English
CAMPHORIC ACID, (±)-
Common Name English
NSC-174634
Code English
1,3-CYCLOPENTANEDICARBOXYLIC ACID, 1,2,2-TRIMETHYL-, (1R,3S)-REL-
Common Name English
Code System Code Type Description
NCI_THESAURUS
C45678
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
CONCEPT Industrial Aid
ECHA (EC/EINECS)
226-404-9
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
SMS_ID
100000076604
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
EPA CompTox
DTXSID301021163
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
MERCK INDEX
m3005
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY Merck Index
WIKIPEDIA
CAMPHORIC ACID
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
NSC
60219
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
NSC
174634
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
FDA UNII
32K0C7JGCJ
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
EVMPD
SUB13219MIG
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
ChEMBL
CHEMBL1205405
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
CAS
5394-83-2
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
NCI_THESAURUS
C87257
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
PUBCHEM
101807
Created by admin on Fri Dec 15 16:17:17 UTC 2023 , Edited by admin on Fri Dec 15 16:17:17 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP