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Cyclohexylmethanol is an organic compound with the formula C 6 H 11 −CH 2 −OH. It is a cyclohexane ring functionalized with an alcohol , specifically a hydroxymethyl group. The compound is a colorless liquid, although commercial samples can appear yellow.
Typical synthesis starts from myrcene [2] and involves a Diels–Alder reaction with acrolein to produce the cyclohexenecarbaldehyde group, this species is marketed as a fragrance in its own right, most commonly under the name 'myrac aldehyde'.
Cyclohexene is a hydrocarbon with the formula (CH 2) 4 C 2 H 2. It is an example of a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commercial synthesis of nylon. [3]
Cyclohexane is a cycloalkane with the molecular formula C 6 H 12.Cyclohexane is non-polar.Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used).
Cyclohexanecarboxylic acid is the organic compound with the formula C 6 H 11 CO 2 H. It is the carboxylic acid of cyclohexane . It is a colorless oil that crystallizes near room temperature.
Cyclohexanehexone, also known as hexaketocyclohexane and triquinoyl, is an organic compound with formula C 6 O 6, the sixfold ketone of cyclohexane.It is an oxide of carbon (an oxocarbon), a hexamer of carbon monoxide.
3-(4-Carboxybenzoyl)quinoline-2-carboxaldehyde (CBQCA) is a fluorogenic amine labeling dye that is not fluorescent itself, but covalently reacts with primary amines to form fluorescent products. [1] It was first reported in 1991. [2] CBQCA is largely used in the context of quantifying peptides or proteins.