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
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
| 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 |
Camphoric acid is a product of oxidation of camphor, naturally occurring in rosemary. In the early twentieth century, camphoric acid was used in the night-sweats of phthisis and was also employed in solution as a local antiseptic to the nose, throat, and bladder. Camphoric acid was found to induce the expression of glutamate receptors NMDAR1, GluR3/4, and mGluR8.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Multifunctional homochiral lanthanide camphorates with mixed achiral terephthalate ligands. | 2010-10-18 |
|
| Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid. | 2010-09-21 |
|
| Progresses in TCM metal-based antitumour agents. | 2010-06 |
|
| Synthesis of (1R,4S,6R)-5,5,6-trimethyl-2-phosphabicyclo[2.2.2]octane and derivatives. | 2010-04-28 |
|
| Poly[(μ(3)-camphorato-κO:O':O'')(2-methyl-1H-imidazole-κN)zinc(II)]. | 2010-03-03 |
|
| Alteration of molecular conformations, coordination modes, and architectures for a novel 3,8-diimidazol-1,10-phenanthroline compound in the construction of cadmium(II) and zinc(II) homochiral coordination polymers involving an auxiliary chiral camphorate ligand. | 2009-05-18 |
|
| Ionothermal synthesis of homochiral framework with acetate-pillared cobalt-camphorate architecture. | 2008-07-07 |
|
| 2-Amino-pyrimidinium picrate. | 2007-12-06 |
|
| Assembly of a homochiral, body-centered cubic network composed of vertex-shared Mg12 cages: use of electrospray ionization mass spectrometry to monitor metal carboxylate nucleation. | 2007-11-07 |
|
| (1R,3S)-Camphoric acid as a building block in supramolecular chemistry: adducts with organic polyamines. | 2003-02 |
|
| (1R,3S)-Camphoramic acid. | 2002-02 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:24:04 GMT 2025
by
admin
on
Mon Mar 31 18:24:04 GMT 2025
|
| Record UNII |
32K0C7JGCJ
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C45678
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
CONCEPT | Industrial Aid | ||
|
226-404-9
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
560-05-4
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
SUPERSEDED | |||
|
100000076604
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
DTXSID301021163
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
m3005
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | Merck Index | ||
|
CAMPHORIC ACID
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
60219
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
174634
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
32K0C7JGCJ
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
SUB13219MIG
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
CHEMBL1205405
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
5394-83-2
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY | |||
|
C87257
Created by
admin on Mon Mar 31 18:24:04 GMT 2025 , Edited by admin on Mon Mar 31 18:24:04 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ENANTIOMER -> RACEMATE |
|
||
|
|
ENANTIOMER -> RACEMATE |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|