Chemistry:Cyclohexanecarboxylic acid
| |
| Names | |
|---|---|
| Preferred IUPAC name
Cyclohexanecarboxylic acid[1] | |
| Identifiers | |
3D model (JSmol)
|
|
| ChEBI | |
| ChemSpider | |
PubChem CID
|
|
| UNII | |
| |
| |
| Properties | |
| C7H12O2 | |
| Molar mass | 128.171 g·mol−1 |
| Appearance | white solid |
| Density | 1.0274 g/cm3 |
| Melting point | 30–31 °C (86–88 °F; 303–304 K) |
| Boiling point | 232–234 °C (450–453 °F; 505–507 K) |
| −83.24·10−6 cm3/mol | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Cyclohexanecarboxylic acid is the organic compound with the formula C6H11CO2H. It is the carboxylic acid of cyclohexane. It is a colorless oil that crystallizes near room temperature.[2]
Preparation and reactions
It is prepared by hydrogenation of benzoic acid.
Cyclohexanecarboxylic acid is a precursor to the nylon-6 precursor caprolactam via its reaction with nitrosylsulfuric acid. It can also be oxidized to cyclohexene.[2]
Cyclohexanecarboxylic acid exhibits the reactions typical of carboxylic acids, including its conversion to the acid chloride cyclohexanecarbonyl chloride using thionyl chloride[3] or oxalyl chloride[4] and to various other acyl derivatives either directly or by way of the acyl halide.
Biochemistry
Cyclohexanecarboxylic acid is a product in the metabolism of benzoic acid in certain microorganisms.[5] In rat models, cyclohexanecarboxylic acid was found to have anti-convulsant acitvity in a manner similar to valproic acid.[6]
Related compounds
Derivatives related to cyclohexanecarboxylic acid include:
- Category:Cyclohexanecarboxylic acids—chemicals having substituents on the cyclohexane ring
External links
- Cyclohexanecarboxylic+Acids at the US National Library of Medicine Medical Subject Headings (MeSH)
References
- ↑ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 303,639. doi:10.1039/9781849733069-00648. ISBN 978-0-85404-182-4.
- ↑ 2.0 2.1 Maki, Takao; Takeda, Kazuo. "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_555..
- ↑ Cope, Arthur C.; Ciganek, Engelbert (1959). "N,N-Dimethylcyclohexylmethylamine". Organic Syntheses 39: 19. doi:10.15227/orgsyn.039.0019.
- ↑ Spessard, Gary O.; Chan, Wan Kit; Masamune, S. (1983). "Preparation of thiol esters: S-tert-butyl cyclohexanecarbothioate and S-tert-butyl 3α,7α,12α-trihydroxy-5β-cholane-24-thioate". Organic Syntheses 61: 134. doi:10.15227/orgsyn.061.0134.
- ↑ Elshahed, M. S.; Bhupathiraju, V. K.; Wofford, N. Q.; Nanny, M. A.; McInerney, M. J. (2001). "Metabolism of benzoate, cyclohex-1-ene carboxylate, and cyclohexane carboxylate by "Syntrophus aciditrophicus" strain SB in syntrophic association with H2-using microorganisms". Applied and Environmental Microbiology 67 (4): 1728–1738. doi:10.1128/AEM.67.4.1728-1738.2001. PMID 11282627.
- ↑ Liu, M. J.; Pollack, G. M. (1994). "Pharmacokinetics and pharmacodynamics of valproate analogues in rats. IV. Anticonvulsant action and neurotoxicity of octanoic acid, cyclohexanecarboxylic acid, and 1-methyl-1-cyclohexanecarboxylic acid". Epilepsia 35 (1): 234–243. doi:10.1111/j.1528-1157.1994.tb02939.x. PMID 8112253.
 |  |
