(2S,5R)-Benzyl 5-amino-2-methylpiperidine-1-carboxylate

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Reagent Code: #36588
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CAS Number 1207947-49-6

science Other reagents with same CAS 1207947-49-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.32 g/mol
Formula C₁₄H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD28968064
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the pharmaceutical and research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a benzyl group and a piperidine ring, makes it a versatile building block for the development of drugs targeting the central nervous system (CNS). It is often employed in the preparation of compounds with potential therapeutic effects, such as analgesics, antipsychotics, or anti-inflammatory agents. Additionally, its chiral centers allow for the creation of enantiomerically pure substances, which are crucial in designing drugs with high specificity and reduced side effects. Researchers also use it in the study of receptor-ligand interactions to better understand biochemical pathways and drug mechanisms.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿756.00

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(2S,5R)-Benzyl 5-amino-2-methylpiperidine-1-carboxylate
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This compound is primarily utilized in the pharmaceutical and research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a benzyl group and a piperidine ring, makes it a versatile building block for the development of drugs targeting the central nervous system (CNS). It is often employed in the preparation of compounds with potential therapeutic effects, such as analgesics, antipsychotics, or anti-inflammatory agents. Additionally, its chiral centers allow for the creation of enantiomerically pure substances, which are crucial in designing drugs with high specificity and reduced side effects. Researchers also use it in the study of receptor-ligand interactions to better understand biochemical pathways and drug mechanisms.
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