ChemicalBook CAS DataBase List Cyclohexanol

Cyclohexanol synthesis

15synthesis methods

Product Name:Cyclohexanol
CAS Number:108-93-0
Molecular formula:C6H12O
Molecular Weight:100.16

Cyclohexanol is prepared by the catalytic air oxidation of cyclohexane or by the catalytic hydrogenation of phenol. The most important use of cyclohexanol is in producing adipic acid used in the manufacture of caprolactam. Cyclohexanol is used in the manufacture of esters for use as plasticizers; it is also used as a chemical intermediate, a stabilizer, a homogenizer for various soap and detergent emulsions, and as a solvent for lacquers and varnishes . The primary routes of occupational exposure are dermal and inhalation.

108-95-2 Synthesis

108-95-2
778 suppliers
$14.00/25g

108-93-0
443 suppliers
$11.00/25g

Yield:108-93-0 100%

Reaction Conditions:

in methanol;water;

Steps:

5 Hydrogenation of Phenol

Hydrogenation of phenol was performed in the same manner as in Example 1 except that 2.0 g of the R-Ru catalyst prepared in Example 1, 2.5 g of phenol, 15 g of deionized water, and 15 g of methanol were used, the reaction temperature was from room temperature without an increase, and the reaction time was 0.7 hour. The reaction results were as follows. Phenol conversion was 100%, and yield of cyclohexanol was 99.8% by mole.

References:

US6018048,2000,A

91-10-1 Synthesis

91-10-1
404 suppliers
$7.00/1g

108-93-0
443 suppliers
$11.00/25g

References

Benzene, 1-[(cyclohexyloxy)methyl]-4-methoxy-

156147-58-9
0 suppliers
inquiry

108-93-0
443 suppliers
$11.00/25g

References

62-53-3 Synthesis

62-53-3
682 suppliers
$10.00/1g

108-93-0
443 suppliers
$11.00/25g

References

108-94-1 Synthesis

108-94-1
594 suppliers
$12.00/50g

108-93-0
443 suppliers
$11.00/25g

References

Cyclohexanol Related Search:

2-Aminocyclohexanol Dicyclohexylamine 1-Ethynyl-1-cyclohexanol Cyclohexanone Cyclohexylamine trans-4-Aminocyclohexanol 2-(1-HydroxyCyclohexyl)-2-(4-MethoxyPhenyl)Acetonitrile Cyclohexyl acetate CYCLOHEXANOL-D12 Venlafaxine

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Cyclohexanol synthesis

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