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Product Introduction
Physical and Chemical Properties
Cyclohexanone is the organic compound with the formula (CH2)5CO. The molecule consists of a six-carbon cyclic molecule with a ketone functional group. This colorless oily liquid has an odor reminiscent of acetone. Over time, samples of cyclohexanone assume a pale yellow color. Cyclohexanone is slightly soluble in water and miscible with common organic solvents.
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a.The great majority of cyclohexanone is consumed in the production of precursors to Nylon 6,6 and Nylon 6.
b.The cyclohexanone supply is converted to cyclohexanone oxime.
c.Laboratory reactions.In addition to the large scale reactions conducted in service of the polymer industry, many reactions have been developed for cyclohexanone. In the presence of light, it undergoes alpha-chlorination to give 2-chlorocyclohexanone. It forms a trimethylsilylenol ether upon treatment with trimethylsilylchloride in the presence of base. It also forms an enamine with pyrrolidine.
d.Cyclohexanone has been used in the production of phencyclidine and its analogs.
Storage
Like cyclohexanol, cyclohexanone is not carcinogenic and is moderately toxic, with a TLV of 25 ppm for the vapor. It is an irritant.
Cyclohexanone is the organic compound with the formula (CH2)5CO. The molecule consists of a six-carbon cyclic molecule with a ketone functional group. This colorless oily liquid has an odor reminiscent of acetone. Over time, samples of cyclohexanone assume a pale yellow color. Cyclohexanone is slightly soluble in water and miscible with common organic solvents.
ApplicatioIt seems that the text you provided is incomplete or not visible. Please provide the text you would like to have translated, and I'll be happy to assist you.
a.The great majority of cyclohexanone is consumed in the production of precursors to Nylon 6,6 and Nylon 6.
b.The cyclohexanone supply is converted to cyclohexanone oxime.
c.Laboratory reactions.In addition to the large scale reactions conducted in service of the polymer industry, many reactions have been developed for cyclohexanone. In the presence of light, it undergoes alpha-chlorination to give 2-chlorocyclohexanone. It forms a trimethylsilylenol ether upon treatment with trimethylsilylchloride in the presence of base. It also forms an enamine with pyrrolidine.
d.Cyclohexanone has been used in the production of phencyclidine and its analogs.
Storage
Like cyclohexanol, cyclohexanone is not carcinogenic and is moderately toxic, with a TLV of 25 ppm for the vapor. It is an irritant.
