1-Piperidin-1-yl-cyclohexanecarboxylic acid

≥95%

Reagent Code: #227958
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CAS Number 898379-76-5

science Other reagents with same CAS 898379-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.31 g/mol
Formula C₁₂H₂₁NO₂
badge Registry Numbers
MDL Number MFCD05230543
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block for ligands in medicinal chemistry due to its rigid cyclohexane backbone and the presence of a piperidine group, which can enhance binding affinity to biological targets. Commonly employed in the synthesis of receptor modulators, including those targeting central nervous system disorders. Also utilized in the preparation of novel analogs for structure-activity relationship studies. Its amide derivatives are explored in drug discovery for improved metabolic stability and bioavailability.

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inventory 5mg
10-20 days ฿9,100.00

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1-Piperidin-1-yl-cyclohexanecarboxylic acid
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block for ligands in medicinal chemistry due to its rigid cyclohexane backbone and the presence of a piperidine group, which can enhance binding affinity to biological targets. Commonly employed in the synthesis of receptor modulators, including those targeting central nervous system disorders. Also utilized in the preparation of novel analogs for structure-activity relations

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block for ligands in medicinal chemistry due to its rigid cyclohexane backbone and the presence of a piperidine group, which can enhance binding affinity to biological targets. Commonly employed in the synthesis of receptor modulators, including those targeting central nervous system disorders. Also utilized in the preparation of novel analogs for structure-activity relationship studies. Its amide derivatives are explored in drug discovery for improved metabolic stability and bioavailability.

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