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Methoxy, (cyclohexyloxy)oxo- is a chemical compound with the molecular formula C13H23NO3. It is an organic compound that features a methoxy group (-OCH3), a cyclohexyloxy group (-O-C6H11), and an oxo group (=O). Methoxy, (cyclohexyloxy)oxo- is characterized by its unique structure, which consists of a cyclohexane ring with an oxygen atom attached to one of its carbons, forming a cyclohexyloxy group. Additionally, the molecule contains a carbonyl group (C=O) and a methoxy group attached to the same carbon atom, making it a potentially versatile intermediate in organic synthesis. The compound may have applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique functional groups and structural features.

4567-86-6

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4567-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4567-86-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,6 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4567-86:
(6*4)+(5*5)+(4*6)+(3*7)+(2*8)+(1*6)=116
116 % 10 = 6
So 4567-86-6 is a valid CAS Registry Number.

4567-86-6Downstream Products

4567-86-6Relevant academic research and scientific papers

THERMAL DECOMPOSITION OF DICYCLOHEXYLPEROXYDICARBONATE IN DIFFERENT TYPES OF SOLVENTS

Kartasheva, Z. S.,Kasaikina, O. T.

, p. 37 - 43 (1991)

We have obtained data on the rates of homolysis and induced decomposition of dicyclohexyldicarbonate (PC) in different types of solvents: n-decane, cyclohexane, chlorobenzene, acetonitrile.The rate of induced decomposition is determined by the activity of the radicals formed from the solvent.We have established that benzene and chlorobenzene participate in radical reactions of induced decomposition of PC, which leads to formation of a number of isomeric aryl-containing compounds.

Synthesis of peroxydicarbonates containing alkyl-aromatic fragments and investigation of their properties

Etlis, I.V.,Fomin, V.A.,Nozrina, F.D.

, p. 2010 - 2015 (2007/10/02)

The reaction of alkyl-substituted benzyl- and naphthylmethyl-chloroformates with Na2O2 or cyclohexyloxyperoxycarbonic acid at 0-5 deg C leads to symmetric and asymmetric peroxydicarbonates.Investigation of the thermolysis kinetics of the peroxides at 50-70 deg C showed that the structure of the organic fragment influences the rate of homolysis of the O-O bond to a great extent.This is characteristic in particular for compounds containing substituents in the ortho-position, where the presence of methyl radicals leads to a decrease in the contribution of the induced dissociation to the overall rate of homolysis of the peroxides obtained

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