CAMPHORIC ACID, (+)-

Details

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

SHOW SMILES / InChI

Structure Search

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

Description
Sources: https://www.henriettes-herb.com/eclectic/bpc1911/acidum-camp.html | https://www.sciencedirect.com/science/article/pii/B9781845690175500075 | https://www.ncbi.nlm.nih.gov/pubmed/19034607

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
(1R,3S)-Camphoramic acid.	2002 Feb	11828124
(1R,3S)-Camphoric acid as a building block in supramolecular chemistry: adducts with organic polyamines.	2003 Feb	12554977
2-Amino-pyrimidinium picrate.	2007 Dec 6	21200681
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 Nov 7	17927183
Ionothermal synthesis of homochiral framework with acetate-pillared cobalt-camphorate architecture.	2008 Jul 7	18537237
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 May 18	19351172
Synthesis of (1R,4S,6R)-5,5,6-trimethyl-2-phosphabicyclo[2.2.2]octane and derivatives.	2010 Apr 28	20372709
Progresses in TCM metal-based antitumour agents.	2010 Jun	20545619
Poly[(μ(3)-camphorato-κO:O':O'')(2-methyl-1H-imidazole-κN)zinc(II)].	2010 Mar 3	21580467
Multifunctional homochiral lanthanide camphorates with mixed achiral terephthalate ligands.	2010 Oct 18	20845984
Chiral gels derived from secondary ammonium salts of (1R,3S)-(+)-camphoric acid.	2010 Sep 21	20978610

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:51:17 GMT 2023` Edited by `admin` on `Fri Dec 15 15:51:17 GMT 2023`
Record UNII	W77RM1CSD5
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

CAMPHORIC ACID, (+)-

Common Name

English

CAMPHORIC ACID D-FORM [MI]

Common Name

English

(1R,3S)-(+)-CAMPHORIC ACID

Systematic Name

English

1,3-CYCLOPENTANEDICARBOXYLIC ACID, 1,2,2-TRIMETHYL-, (1R,3S)-

Common Name

English

CAMPHORIC ACID 1-METHYL ESTER

Systematic Name

English

(1R,3S)-CAMPHORIC ACID

Systematic Name

English

(1R,3S)-1,2,2-TRIMETHYL-1,3-CYCLOPENTANEDICARBOXYLIC ACID

Systematic Name

English

1,3-CYCLOPENTANEDICARBOXYLIC ACID, 1,2,2-TRIMETHYL-, (1R-CIS)-

Common Name

English

CAMPHORIC ACID D-FORM

Common Name

English

D-(+)-CAMPHORIC ACID

Common Name

English

D-CAMPHORIC ACID

Common Name

English

CAMPHORIC ACID, D-

Common Name

English

CAMPHORICUM ACIDUM [HPUS]

Common Name

English

DEXTROCAMPHORIC ACID

Common Name

English

Code System Code Type Description

EPA CompTox

DTXSID60883316