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1-<(Cyclohexylamino)methyl>cyclohexanol is a complex organic compound with the molecular formula C13H25NO. It features a cyclohexanol group (a cyclohexane ring with a hydroxyl group) connected to a cyclohexylamine group (a cyclohexane ring with an amino group) through a methylene bridge. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, particularly those with complex ring structures. Its unique structure allows for various chemical reactions and modifications, making it a valuable intermediate in organic chemistry.

7592-90-7

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7592-90-7 Usage

Chemical class

Cyclohexanols

Molecular weight

211.34 g/mol

Structure

Cyclohexane ring with a hydroxyl group and an amino group attached

Pharmaceutical industry use

Intermediate in the synthesis of various drugs

Organic synthesis use

Reagent in organic synthesis

Solvent use

Solvent for organic reactions

Potential applications

Medicinal chemistry and drug development due to unique chemical structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 7592-90-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7592-90:
(6*7)+(5*5)+(4*9)+(3*2)+(2*9)+(1*0)=127
127 % 10 = 7
So 7592-90-7 is a valid CAS Registry Number.

7592-90-7Relevant academic research and scientific papers

Preparation of Vicinal N-Alkylamino Alcohols via Acylation-Rearrangement of Nitrones Followed by Hydride Reduction

Coates, Robert M.,Cummins, Clark H.

, p. 1383 - 1389 (2007/10/02)

Acylation-rearrangement of N-tert-butyl and N-cyclohexyl nitrones of cyclohexanecarboxaldehyde (1), n-butyraldehyde, isobutyraldehyde, 3-cyclohexenecarboxaldehyde, and α-methylpropionaldehyde gave α-pivaloyloxy imines, which underwent reduction with lithi

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