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3-Cyclohexyl-1,2-dihydroxybenzene is an organic compound with the molecular formula C13H16O2. It is a white crystalline solid that is soluble in organic solvents. 3-cyclohexyl-1,2-dihydroxybenzene is characterized by a benzene ring with two hydroxyl groups at the 1 and 2 positions, and a cyclohexyl group attached at the 3 position. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain herbicides and insecticides. Due to its chemical structure, it exhibits specific reactivity and can participate in a range of chemical transformations, making it a valuable building block in organic chemistry.

1133-62-6

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1133-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1133-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1133-62:
(6*1)+(5*1)+(4*3)+(3*3)+(2*6)+(1*2)=46
46 % 10 = 6
So 1133-62-6 is a valid CAS Registry Number.

1133-62-6Downstream Products

1133-62-6Relevant academic research and scientific papers

Synthesis of cyclohexylphenols

Postnova,Koshel',Lebedeva,Kuznetsova,Koshel'

, p. 1415 - 1417 (2007/10/03)

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.

Medium-scale preparation of useful metabolites of aromatic compounds via whole-cell fermentation with recombinant organisms

Endoma, Mary Ann,Bui, Vu P.,Hansen, Jeff,Hudlicky, Tomas

, p. 525 - 532 (2013/09/06)

The whole-cell fermentation of aromatic coumpounds with Escherichia coli JM109 (pDTG601) on a medium scale (10-15L) produces enantiopure cyclohexadienediols. A detailed procedure for the fermentation is described, and yields for several metabolites are provided. A similar procedure using E. coli JM109 (pDTG602) affords catechols. The dienediols are useful for asymmetric synthesis, and several important targets originating from these metabolites are tabulated.

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

Kozlikovskii, Ya. B.,Koshchii, V. A.,Butov, S. A.,Ovsiyuk, T. F.

, p. 746 - 749 (2007/10/02)

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.

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