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Methyl 2-[(1H-pyrrolo[2,3-b]pyridin-5-yl)oxy]-4-[4-[[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-enyl]

Category:

Intermediates&Fine Chemicals

CAS NO:

1235865-76-5

Standard:

In-house Standards,

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Basic Info

CAS Number

1235865-76-5

Pharmacopoeia

In-house Standards

Grade

Pharmaceutical Grade

Product Keywords

Methyl 2-[(1H-pyrrolo[2,3-b]pyridin-5-yl)oxy]-4-[4-[[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-enyl]

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Product Description

英文名称： Methyl 2-[(1H-pyrrolo[2,3-b]pyridin-5-yl)oxy]-4-[4-[[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-enyl]methyl]piperazin-1-yl]benzoate
别名：
CAS号： 1235865-76-5
分子式： C34H37ClN4O3
分子量： 585.14

AI Product Description

*The following content is generated by AI and is for reference only.

The chemical entity described corresponds to a complex organic structure featuring a pyrrolo[2,3-b]pyridine core linked via an ether bond to a substituted cyclohexene ring. While the specific name provided in the query appears to be an incomplete IUPAC string lacking the final ester or functional group designation for the cyclohexene moiety (indicated by the trailing quotation mark), it closely resembles intermediates used in medicinal chemistry for kinase inhibitor development. Based on structural analysis of similar compounds, this class of molecules typically targets protein kinases involved in cell signaling pathways, particularly those regulating tumor growth and metastasis. In terms of physical properties, such heterocyclic compounds are generally characterized as crystalline solids with moderate solubility in organic solvents like dimethyl sulfoxide (DMSO) or dichloromethane, while exhibiting low solubility in aqueous media. The presence of the chlorophenyl and dimethylcyclohexene groups suggests high lipophilicity, which is crucial for membrane permeability in biological assays. Although a precise CAS number cannot be assigned without the complete molecular formula due to potential variations in the terminal functional group, analogous structures often possess CAS identifiers within the range of 10^6 to 10^7, reflecting their status as specialized synthetic research materials rather than commercial bulk chemicals. These compounds are primarily utilized in pharmaceutical research laboratories as lead compounds or pharmacological probes. Their main application lies in oncology research, where they serve as inhibitors for specific tyrosine kinases, potentially halting uncontrolled cell proliferation associated with various cancers. Researchers employ these molecules in vitro to screen for binding affinity against target proteins and in vivo to evaluate efficacy in animal models of disease. Furthermore, the structural complexity involving the fused pyrrole-pyridine system offers a versatile scaffold for optimizing potency and selectivity through rational drug design. Due to their specialized nature, they are not intended for consumer use but are strictly handled under controlled laboratory conditions. Synthesis typically involves multi-step organic reactions including nucleophilic aromatic substitution and palladium-catalyzed coupling, requiring expertise in organic synthesis. As the field advances, derivatives of this scaffold may contribute to the next generation of targeted cancer therapies, offering improved therapeutic indices over traditional chemotherapy agents.