18530-30-8

Basic information

• Product Name: (+)-CAMPHORCARBOXYLIC ACID
• Synonyms: (+)-CAMPHORCARBOXYLIC ACID;bismuth tris(2-oxobornane-3-carboxylate);d-Camphocarboxylic acid;(+)-CAMPHORCARBOXYLIC ACID 98%;[1S,4β,(+)]-2-Oxobornane-3-carboxylic acid;Einecs 242-404-1
• CAS NO: 18530-30-8
• Molecular Formula: C₁₁H₁₆O₃
• Molecular Weight: 196.24
• EINECS: 242-404-1
• Mol File: 18530-30-8.mol
• Article Data: 1

Chemical Properties

• Melting Point: 127-128°
• Boiling Point: 273.13°C (rough estimate)
• Flash Point: 160.1 °C
• Appearance: /
• Density: 1.0962 (rough estimate)
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.4600 (estimate)
• PKA: 3.57±0.60(Predicted)
• CAS DataBase Reference: (+)-CAMPHORCARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-CAMPHORCARBOXYLIC ACID(18530-30-8)
• EPA Substance Registry System: (+)-CAMPHORCARBOXYLIC ACID(18530-30-8)

Safety Data

• Hazardous Substances Data: 18530-30-8(Hazardous Substances Data)

Usage

General Description

(+)-Camphorcarboxylic acid, also known as camphoric acid, is a naturally occurring compound that can be found in plants such as the camphor tree. It is a white, crystalline solid and has a camphor-like odor. Chemically, it is a carboxylic acid and is commonly used in the production of pharmaceuticals and fragrances. It has been reported to have antimicrobial properties and is used in the synthesis of various drugs. Additionally, it is known to exhibit anti-inflammatory and anti-oxidant activities, making it a valuable compound in the field of medicinal chemistry. Overall, camphoric acid is a versatile chemical with a wide range of potential applications in various industries.

InChI:InChI=1/C11H16O3/c1-10(2)6-4-5-11(10,3)8(12)7(6)9(13)14/h6-7H,4-5H2,1-3H3,(H,13,14)/t6-,7+,11+/m1/s1

Upstream product

• 124-38-9 carbon dioxide 
• 736109-58-3 1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one 
• 76-22-2 Camphor 
• 15719-64-9 methylammonium carbonate 

Downstream Products

• 81925-14-6 (1R,2S,4S,6S,7R)-4-Benzhydryloxy-1,10,10-trimethyl-3-oxa-tricyclo[5.2.1.0^2,6]decane 
• 81925-14-6 <2R-(2α,3aα,4α,7α,7aα)>-2,3,3a,4,5,6,7,7a-Octahydro-2-(1,1-diphenylmethoxy)-7,8,8-trimethyl-4,7-methanobenzofuran 
• 81925-13-5 (1R,2S,4R,6S,7R)-4-Cyclohexyloxy-1,10,10-trimethyl-3-oxa-tricyclo[5.2.1.0^2,6]decane 
• 81925-13-5 <2S-(2α,3aα,4α,7α,7aα)>-2,3,3a,4,5,6,7,7a-Octahydro-2-cyclohexyloxy-7,8,8-trimethyl-4,7-methanobenzofuran 
• 81969-34-8 (1R-endo)-1,7,7-Trimethyl-3-<(4-methylphenyl)sulfonyloxymethyl>bicyclo<2.2.1>heptan-2-on 
• 81925-04-4 <1R-(endo,exo)>-3-Hydroxy-4,7,7-trimethylbicyclo<2.2.1>heptan-2-essigsaeure 
• 81969-26-8 <1R-(endo,endo)>-3-Hydroxy-4,7,7-trimethylbicyclo<2.2.1>heptan-2-methanol,4-Methylbenzolsulfonat 
• 24399-00-6 <1R-(endo,exo)>-3-Hydroxy-4,7,7-trimethylbicyclo<2.2.1>heptan-2-methanol,4-Methylbenzolsulfonat 
• 129940-80-3 2-oxobornan-3-carbonyl chloride 

Relevant articles and documents

Synthesis and local anesthetic activity of some derivatives of N,N-diethyl-2-(2-alkoxyphenylcarbamoyloxy)bornan-3-ylmethyl-ammonium chlorides

A series of 8 new esters of 2-alkoxyphenyl-carbamoic acid were synthesized and assayed for local anesthetic activity. All compounds were isolated as hydrochlorides and their structure was proved by 1H-NMR 13C-NMR and IR spectroscopy. The index of anesthetic activity in infiltration and surface anesthesia proved that all prepared compounds are significantly more active than the standard reference compounds, procaine and cocaine, respectively; it is tightly correlated with the length of the alkoxy group. It was found that there is a parabolic relationship between log activity and molecular lipophilicity (as measured by R(M)). Toxicity of all compounds is within acceptable limits.