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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. [3] [4]
Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44 –3.9 Acetic acid: 1.04 117.9 3.14 16.6 –3.90 K b [1] K f [2] Acetone: 0.78 56.2 1.67 –94.8 K b [3] Benzene: 0.87 80.1 2.65 5.5 –5.12 K b & K f [2] Bromobenzene: 1.49 156.0 6. ...
Melting point: 19 °C (66 °F) [1] Boiling point: 187–188 °C (369–370 °F) [3] Solubility in water. small in water [4] Hazards Flash point:
Melting point: 185 to 187 °C (365 to 369 °F; 458 to 460 K) ... is a cyclohexene, a cyclitol and a cyclohexanecarboxylic acid. ... Starting point in the biosynthesis ...
Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid.
Triple point: 279.48 K (6.33 °C), 5.388 kPa [3] Critical point: 554 K (281 °C), 4070 kPa Std enthalpy change of fusion, Δ fus H o: 2.68 kJ/mol crystal I → liquid Std entropy change of fusion, Δ fus S o: 9.57 J/(mol·K) crystal I → liquid Std enthalpy change of vaporization, Δ vap H o: 32 kJ/mol Std entropy change of vaporization, Δ ...
Pages in category "Cyclohexanecarboxylic acids" The following 7 pages are in this category, out of 7 total. ... 3-Dehydroquinic acid; Dicycloverine; Q. Quinic acid; S.
Cyclohexane has two crystalline phases. The high-temperature phase I, stable between 186 K and the melting point 280 K, is a plastic crystal, which means the molecules retain some rotational degree of freedom. The low-temperature (below 186 K) phase II is ordered.