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 |
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(1R,3S)-Camphoramic acid. | 2002 Feb |
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(1R,3S)-Camphoric acid as a building block in supramolecular chemistry: adducts with organic polyamines. | 2003 Feb |
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2-Amino-pyrimidinium picrate. | 2007 Dec 6 |
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Synthesis of (1R,4S,6R)-5,5,6-trimethyl-2-phosphabicyclo[2.2.2]octane and derivatives. | 2010 Apr 28 |
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Progresses in TCM metal-based antitumour agents. | 2010 Jun |
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Poly[(μ(3)-camphorato-κO:O':O'')(2-methyl-1H-imidazole-κN)zinc(II)]. | 2010 Mar 3 |
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Multifunctional homochiral lanthanide camphorates with mixed achiral terephthalate ligands. | 2010 Oct 18 |
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Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid. | 2010 Sep 21 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:17:16 GMT 2023
by
admin
on
Fri Dec 15 16:17:16 GMT 2023
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Record UNII |
32K0C7JGCJ
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Record Status |
Validated (UNII)
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Record Version |
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C45678
Created by
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CONCEPT | Industrial Aid | ||
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226-404-9
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100000076604
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DTXSID301021163
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m3005
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PRIMARY | Merck Index | ||
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CAMPHORIC ACID
Created by
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60219
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174634
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32K0C7JGCJ
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SUB13219MIG
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CHEMBL1205405
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5394-83-2
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C87257
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101807
Created by
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PRIMARY |
Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE |
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ENANTIOMER -> RACEMATE |
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Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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