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5-Cyclohexyl-valeric acid amide is a chemical compound with the molecular formula C11H19NO. It is a derivative of valeric acid, which is a saturated monocarboxylic acid with a five-carbon chain. The cyclohexyl group is attached to the fifth carbon atom of the valeric acid chain, and an amide group (-CONH2) replaces the carboxylic acid group (-COOH) at the end of the chain. 5-cyclohexyl-valeric acid amide is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique structural properties. It is synthesized through a series of chemical reactions, often involving the formation of an amide bond between the carboxylic acid and an amine. The compound's specific applications and properties can vary depending on the context in which it is used, but it is generally recognized for its ability to form stable structures and its potential to interact with other molecules in biological systems.

5962-87-8

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5962-87-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5962-87-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5962-87:
(6*5)+(5*9)+(4*6)+(3*2)+(2*8)+(1*7)=128
128 % 10 = 8
So 5962-87-8 is a valid CAS Registry Number.

5962-87-8Relevant academic research and scientific papers

Sigma receptor ligands and the use thereof

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, (2008/06/13)

The invention relates to methods for the treatment of central nervous system disorders, gastrointestinal disorders, drug abuse, angina, migraine, hypertension and depression by administering a pharmaceutical composition comprising an effective amount of certain sigma receptor ligands to a patient in need of such treatment. The invention further relates to novel sigma receptor ligands having high binding to the sigma receptor and pharmaceutical compositions thereof. Unexpectedly, certain of the sigma receptor ligands of the present invention have selectivity for the sigma receptor over the DA, PCP and 5-HT1A receptors.

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