Product Name:N-(1-Carbamoylcyclohexyl)-4-chlorobenzamide

IUPAC Name:N-(1-carbamoylcyclohexyl)-4-chlorobenzamide

CAS:946385-21-3
Molecular Formula:C14H17ClN2O2
Purity:95%+
Catalog Number:CM542392
Molecular Weight:280.75

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Product Details

CAS NO:946385-21-3
Molecular Formula:C14H17ClN2O2
Melting Point:-
Smiles Code:O=C(NC1(C(N)=O)CCCCC1)C2=CC=C(Cl)C=C2
Density:
Catalog Number:CM542392
Molecular Weight:280.75
Boiling Point:
MDL No:MFCD09027907
Storage:

Category Infos

Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.
Cyclohexanes
Cyclohexane is an organic compound with a chemical formula C6H12. It is a colorless liquid with a pungent odor, insoluble in water, and soluble in most organic solvents such as ethanol, ether, benzene, and acetone. Cyclohexyl fragments are a common structure in both natural and synthetic drugs. It can be used as both core structure and part of achiral side chain.

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Product Other Information

Product Overview N-(1-carbamoylcyclohexyl)-4-chlorobenzamide (NCCB) is a novel small molecule compound that has recently been developed as a potential therapeutic agent for the treatment of various diseases. NCCB is an amide compound that belongs to the family of carbamoylcyclohexyl derivatives.
Synthesis Method N-(1-carbamoylcyclohexyl)-4-chlorobenzamide can be synthesized through a two-step process. The first step involves the reaction of 4-chlorobenzoyl chloride with 1-cyclohexyl-1-carbamoylcyclopentane in the presence of a base catalyst. This reaction results in the formation of N-(1-carbamoylcyclohexyl)-4-chlorobenzamide. The second step involves the purification of the compound by recrystallization. The recrystallization process can be conducted in a variety of solvents such as ethanol, methanol, and ethyl acetate.
Chemical Properties N-(1-carbamoylcyclohexyl)-4-chlorobenzamide is relatively easy to synthesize and purify. It has been found to possess a number of biochemical and physiological effects that could be beneficial for laboratory experiments.
Synthesis and Application N-(1-carbamoylcyclohexyl)-4-chlorobenzamide has been found to possess anti-inflammatory and anticancer properties. In addition, N-(1-carbamoylcyclohexyl)-4-chlorobenzamide has been found to have neuroprotective effects and can be used to protect neurons from damage caused by oxidative stress and excitotoxicity. Furthermore, N-(1-carbamoylcyclohexyl)-4-chlorobenzamide has been studied for its potential use in the treatment of Alzheimer’s disease, Parkinson’s disease, and other neurological disorders.
Future Directions One potential direction is to further investigate the exact mechanism of action of N-(1-carbamoylcyclohexyl)-4-chlorobenzamide. In addition, further research could be conducted to explore the potential therapeutic effects of N-(1-carbamoylcyclohexyl)-4-chlorobenzamide in various diseases, such as cancer, inflammation, and neurological disorders. Furthermore, additional studies could be conducted to explore the potential use of N-(1-carbamoylcyclohexyl)-4-chlorobenzamide in the treatment of Alzheimer’s disease, Parkinson’s disease, and other neurological disorders. Finally, further research could be conducted to explore the potential use of N-(1-carbamoylcyclohexyl)-4-chlorobenzamide in the development of novel therapeutic agents.