5394-54-7 Usage
Molecular structure
2-[(2-oxocyclohexyl)methoxymethyl]cyclohexan-1-one is a cyclohexanone derivative with a complex structure, consisting of a six-membered carbon ring with a ketone group (C=O) and a methoxymethyl group (OCH3) attached to a cyclohexane ring.
Synonym
Kocour's compound.
Use as a reagent
The compound is used in synthetic organic chemistry for the preparation of various compounds, making it a versatile intermediate in the synthesis of biologically active molecules.
Reactivity
The compound's reactivity allows for the selective modification of other functional groups in organic molecules, which is useful in the synthesis of complex organic compounds.
Potential applications
2-[(2-oxocyclohexyl)methoxymethyl]cyclohexan-1-one has been studied for its potential use in the development of new pharmaceuticals and agrochemicals, and has significant potential for various applications in the fields of pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 5394-54-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5394-54:
(6*5)+(5*3)+(4*9)+(3*4)+(2*5)+(1*4)=107
107 % 10 = 7
So 5394-54-7 is a valid CAS Registry Number.
5394-54-7Relevant academic research and scientific papers
Thiomethylation of ketones by sodium sulphide and formaldehyde
Ulendeyeva,Bayeva,Lyapina,Shmakov,Galkin
, p. 177 - 186 (2007/10/03)
The thiomethylation of propanol, butanol, cyclohexanone and acetophenone with a mixture of formaldehyde and sodium sulphide proceeds at 20°C and normal pressure for 1-7 hr. It has been established that the reactivity of ketones increases in the order butanone-cyclohexanone-propanone-acetophenone. The conversion of sodium sulphide depends on its initial concentration, the nature of the ketone, and the presence in the reaction medium of sodium hydroxide and ethyl alcohol. It has been shown that the reaction proceeds with the preferential formation of keto- and diketosulphides.
