4,6-Dichloro-N-(4,4-dimethylcyclohexyl)-1H-indole-2-carboxamide is a synthetic organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of two chlorine atoms at the 4 and 6 positions of the indole ring contributes to its chemical reactivity and potential biological activity. The amide functional group, indicated by the carboxamide moiety, suggests that this compound may exhibit properties typical of amides, such as hydrogen bonding capabilities. The bulky 4,4-dimethylcyclohexyl substituent enhances its lipophilicity, potentially influencing its pharmacokinetic properties. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its unique structural features that could interact with biological targets. Its specific applications and biological activities would depend on further research and characterization, including studies on its solubility, stability, and interaction with various biological systems.

4,6-DICHLORO-N-(4,4-DIMETHYLCYCLOHEXYL)-1H-INDOLE-2-CARBOXAMIDE

1473450-60-0: 4,6-Dichloro-N-(4,4-dimethylcyclohexyl)-1H-indole-2-carboxamide is a synthetic organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of two chlorine atoms at the 4 and 6 positions of the indole ring contributes to its chemical reactivity and potential biological activity. The amide functional group, indicated by the carboxamide moiety, suggests that this compound may exhibit properties typical of amides, such as hydrogen bonding capabilities. The bulky 4,4-dimethylcyclohexyl substituent enhances its lipophilicity, potentially influencing its pharmacokinetic properties. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its unique structural features that could interact with biological targets. Its specific applications and biological activities would depend on further research and characterization, including studies on its solubility, stability, and interaction with various biological systems.

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CAS 1473450-60-0

4,6-DICHLORO-N-(4,4-DIMETHYLCYCLOHEXYL)-1H-INDOLE-2-CARBOXAMIDE

4,6-DICHLORO-N-(4,4-DIMETHYLCYCLOHEXYL)-1H-INDOLE-2-CARBOXAMIDE

Ref: 10-F504962

NITD-304

Ref: TM-T33683