2138-20-7

Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 73, p. 2225, 1951 DOI: 10.1021/ja01149a088

InChI:InChI=1/C12H16O2/c13-10-6-7-11(12(14)8-10)9-4-2-1-3-5-9/h6-9,13-14H,1-5H2

Upstream product

• 108-93-0 cyclohexanol 
• 108-46-3 recorcinol 
• 542-18-7 cyclohexyl chloride 
• 110-83-8 cyclohexene 
• 37470-92-1 4-chloro-6-cyclohexyl-resorcinol 
• 873399-89-4 2,4-dichloro-6-cyclohexyl-resorcinol 

Downstream Products

• 119415-24-6 2',7'-dicyclohexyl-3',6'-dihydroxy-spiro[phthalan-1,9'-xanthen]-3-one 
• 4396-96-7 bicyclohexyl-2,4-dione 
• 873399-90-7 2-chloro-4-cyclohexyl-resorcinol 
• 37470-92-1 4-chloro-6-cyclohexyl-resorcinol 
• 409317-43-7 4-cyclohexyl-6-nitroso-resorcinol 
• 159977-40-9 5-cyclohexyl-2,4-dihydroxy-deoxybenzoin 
• 717917-51-6 3-cyclohexyl-2,6-dihydroxy-deoxybenzoin 
• 30728-32-6 1-cyclohexyl-2,4-dimethoxy-benzene 
• 68100-23-2 5-cyclohexyl-2,4-dihydroxy-benzophenone 
• 65239-79-4 1-(5-Cyclohexyl-2,4-dihydroxy-phenyl)-2,2,2-trifluoro-ethanone 

Relevant academic research and scientific papers

Cyclohexylation of resorcinol with cyclohexanol catalyzed by tungstophosphoric acid supported zirconia catalysts

We demonstrate a highly active and reusable heterogeneous catalyst system, tungstophosphoric acid (TPA) supported on zirconia (ZrO2), for the cyclohexylation of resorcinol by cyclohexanol to produce value added chemicals such as 2-cyclohexyl resorcinol, 4-cyclohexyl resorcinol and 3-Hydroxy cyclohexyl phenyl ether under liquid phase reaction condition. TPA/ZrO2 catalysts prepared with different TPA loadings (5-30 wt.%) by wet impregnation method and calcined in the temperature range of 650-850°C were characterized by Nitrogen sorption analysis, XRD, FTIR, DTG and DTA, and 31P MAS NMR spectroscopy. Among the catalysts studied, 15 wt.%TPA/ZrO2 catalyst calcined at 750°C gave the highest conversion of resorcinol (51.2%) with the selectivities for 3-Hydroxy cyclohexyl phenyl ether (53.9%) and 2-cyclohexyl resorcinol and 4-cyclohexyl resorcinol together (46.1%) under optimum reaction conditions. However, the selectivity of the products were controlled by varying the reaction conditions. At higher conversion of resorcinol (78.9%), only C-alkylated products were formed at 200°C with 15 wt.%TPA/ZrO2 catalyst calcined at 750°C. The combination of TPA and ZrO2 coupled with calcination temperature offered an excellent platform for the conversion of resorcinol into O-or C-alkylated products.

Abnormal Cannabidiols as agents for lowering intraocular pressure

The present invention provides a method of treating glaucoma or ocular hypertension which comprises applying to the eye of a person in need thereof an amount sufficient to treat glaucoma or ocular hypertension of a compound of formula I wherein Y, Q, Z, R, R1 and R2 are as defined in the specification. The present invention further comprises pharmaceutical compositions, e.g. ophthalmic compositions, including said compound of formula I.

Synthesis of cyclohexylphenols

Catalytic alkylation of phenols with cyclohexanol gives o- and p-cyclohexylphenols as the major products. The effect of temperature, catalyst nature, and reactant concentration on the reaction outcome was studied.

Resorcinol derivatives

The present invention relates to the use of certain resorcinol derivatives as skin lightening agents.

Resorcinol derivatives

The present invention relates to the use of certain resorcinol derivatives as skin lightening agents.

ALKYLATION OF PYROCATECHOL AND RESORCINOL WITH CYCLOHEXENE IN THE PRESENCE OF ALUMINUM PHENOLATE

The alkylation of pyrocatechol and resorcinol with cyclohexene in the presence of aluminum phenolate leads to a mixture of isomeric mono- and dicyclohexyldihydroxybenzenes, in which as a rule the ortho-alkylation products predominate.

Vat dye and sulfur dye compositions

Specific vatting accelerators according to claims 1 and 2 are described. These can be added to a vat dye or sulfur dye composition, or to a dye bath or printing paste containing a vat dye or sulfur dye, by virtue of which an improvement of dye yield, particularly on cellulose materials, is obtained.