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Chemical formula. C 6 H 12 S: Molar mass: 116.22 g·mol −1 ... Cyclohexanethiol is a thiol with the formula C 6 H 11 SH. It is a colorless liquid with a strong odor ...
It is produced by buta-1,3-diene dimerization in a Diels-Alder reaction. [5] [4] The reaction is conducted at 110 - 425 °C at pressures of 1.3 - 100 MPa in the presence of a catalyst.
Cyclohexane is a colourless, flammable liquid with a distinctive detergent-like odor, reminiscent of cleaning products (in which it is sometimes used). Cyclohexane is mainly used for the industrial production of adipic acid and caprolactam, which are precursors to nylon. [5] Cyclohexyl (C 6 H 11) is the alkyl substituent of cyclohexane and is ...
Cyclohexylbenzene is the organic compound with the structural formula C 6 H 5 −C 6 H 11. It is a derivative of benzene with a cyclohexyl substituent (C 6 H 11 ). It is a colorless liquid.
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]
Ethanethiol, commonly known as ethyl mercaptan, is an organosulfur compound with the formula CH 3 CH 2 SH. [5] It is a colorless liquid with a distinct odor. Abbreviated EtSH, it consists of an ethyl group (Et), CH 3 CH 2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of ...
Benzyl mercaptan can be prepared by the reaction of benzyl chloride and thiourea. The initially formed isothiouronium salt must be subjected to alkaline hydrolysis to obtain the thiol. It has been identified in boxwood (Buxus sempervirens L.) and is known to contribute to the smoky aroma of certain wines. [2] It also occurs naturally in coffee.
The molecular formula C 2 H 6 S (molar mass: 62.13 g/mol, exact mass: 62.0190 u) may refer to: Dimethyl sulfide (DMS), or methylthiomethane Ethanethiol , or ethyl mercaptan