Cyclohexanecarboxylic acid is a precursor to the nylon-6 precursor caprolactam via its reaction with nitrosylsulfuric acid. It can also be oxidized to cyclohexene. Cyclohexanecarboxylic acid exhibits the reactions typical of carboxylic acids, including its conversion to the acid chloride cyclohexanecarbonyl chloride. Related compounds
The formation of the cyclohexanecarboxylic acid starter unit of ω-cyclohexyl fatty acids from shikimic acid in A. acidocaldarius and two blocked mutants was similarly examined and found to follow the same biosynthetic course. 66 The combined knowledge of the stereochemical fate of the carbon-bound hydrogens of shikimate in S. collinus with the stereochemical information determined in the A. acidocaldarius blocked mutants was crucial to the ultimate delineation of the stereochemistry of each ...
Cyclohexanecarboxylic acid undergoes microbial degradation by a strain of Antherobacter to form para-hydroxybenzoic acid. Cyclohexanecarboxylic acid undergoes aromatization and converts to Hippuric acid in rat liver extracts in vitro. Cyclohexanecarboxylic acid is the starting reagent for the synthesis of polyketide-type antibiotics, Phoslactomycins.
Cyclohexanecarboxylic acid, also known as hexahydrobenzoic acid or carboxycyclohexane, belongs to the class of organic compounds known as carboxylic acids. Carboxylic acids are compounds containing a carboxylic acid group with the formula -C (=O)OH. Cyclohexanecarboxylic acid is a weakly acidic compound (based on its pKa).
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