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1,3-Dimethylcyclohexane-1,3-dicarboxylic acid, also known as DMCD, is an organic compound with the chemical formula C9H14O4. It is a white crystalline solid that is soluble in water and various organic solvents. DMCD is a derivative of cyclohexane, featuring two methyl groups attached to the first and third carbon atoms, and two carboxylic acid groups at the same positions. 1,3-Dimethylcyclohexan-1,3-dicarbonsaeure is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and properties make it a valuable building block in the development of new compounds with diverse applications.

1135-56-4

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1135-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1135-56-4 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 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1135-56:
(6*1)+(5*1)+(4*3)+(3*5)+(2*5)+(1*6)=54
54 % 10 = 4
So 1135-56-4 is a valid CAS Registry Number.

1135-56-4Relevant academic research and scientific papers

Fluorescence sensing due to allosteric switching of pyrene functionalized cis-cyclohexane-1,3-dicarboxylate

Monahan, Carol,Bien, Jeffrey T.,Smith, Bradley D.

, p. 431 - 432 (1998)

The excimer/monomer fluorescence ratio for a pyrene functionalized cis-cyclohexane-1,3-dicarboxylate decreases upon titration with divalent and monovalent metal cations, as well as strong and weak acids.

Remote Enzyme-Coupled Amine Release

Menger, F. M.,Ladika, M.

, p. 3006 - 3007 (2007/10/02)

A remote enzyme-coupled amine release system has been developed in which biochemical and chemical "demasking" processes are sequentially linked via an enforced 1,3-diaxial disposition.Thus, pig liver esterase hydrolyzes an ester to an acid, and the acid promotes a fast intramolecular cleavage of an amide to an amine.The sequence has potential pharmacokinetic relevance because it allows enzyme-specific discharge of amine-based drugs following their trans-membrane journey as uncharged amides.

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