(1S,2S)-2-(Piperidin-1-yl)cyclohexanamine

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Reagent Code: #113034
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CAS Number 824938-98-9

science Other reagents with same CAS 824938-98-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.31 g/mol
Formula C₁₁H₂₂N₂
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring both piperidine and cyclohexylamine moieties, makes it a valuable building block for creating molecules with potential biological activity. It is often employed in the development of drugs targeting the central nervous system, particularly for conditions like anxiety, depression, and pain management. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for optimizing drug efficacy and reducing side effects. Researchers also explore its use in designing ligands for receptor studies, aiding in the understanding of biochemical pathways and drug mechanisms.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,321.00

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(1S,2S)-2-(Piperidin-1-yl)cyclohexanamine
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This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring both piperidine and cyclohexylamine moieties, makes it a valuable building block for creating molecules with potential biological activity. It is often employed in the development of drugs targeting the central nervous system, particularly for conditions like anxiety, depression, and pain management. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial for optimizing drug efficacy and reducing side effects. Researchers also explore its use in designing ligands for receptor studies, aiding in the understanding of biochemical pathways and drug mechanisms.
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