S-1-Boc-piperidine-3-carboxylic acid

97%

Reagent Code: #234231
label
Alias (S)-Boc-Piperidinic Acid Boc-(S)-3-carboxylic acid Piperidinic Acid 1-Boc-L-Piperidinic Acid
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CAS Number 88495-54-9

science Other reagents with same CAS 88495-54-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.27 g/mol
Formula C₁₁H₁₉NO₄
badge Registry Numbers
MDL Number MFCD02179172
thermostat Physical Properties
Melting Point 159-162 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a key chiral building block for the preparation of biologically active molecules. Its Boc-protected amine and carboxylic acid functional groups allow for selective reactions, making it ideal for peptide coupling and the construction of complex nitrogen-containing heterocycles. It is frequently employed in the development of central nervous system agents, including antidepressants, antipsychotics, and analgesics. The piperidine scaffold is common in drug discovery due to its favorable pharmacokinetic properties, and this derivative enables efficient introduction of the ring in a stereocontrolled manner. Its stability and ease of handling further support its use in multi-step organic syntheses, particularly in the production of small-molecule therapeutics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿150.00
inventory 5g
10-20 days ฿600.00
inventory 25g
10-20 days ฿2,110.00
S-1-Boc-piperidine-3-carboxylic acid
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Widely used in pharmaceutical synthesis, this compound serves as a key chiral building block for the preparation of biologically active molecules. Its Boc-protected amine and carboxylic acid functional groups allow for selective reactions, making it ideal for peptide coupling and the construction of complex nitrogen-containing heterocycles. It is frequently employed in the development of central nervous system agents, including antidepressants, antipsychotics, and analgesics. The piperidine scaffold is c

Widely used in pharmaceutical synthesis, this compound serves as a key chiral building block for the preparation of biologically active molecules. Its Boc-protected amine and carboxylic acid functional groups allow for selective reactions, making it ideal for peptide coupling and the construction of complex nitrogen-containing heterocycles. It is frequently employed in the development of central nervous system agents, including antidepressants, antipsychotics, and analgesics. The piperidine scaffold is common in drug discovery due to its favorable pharmacokinetic properties, and this derivative enables efficient introduction of the ring in a stereocontrolled manner. Its stability and ease of handling further support its use in multi-step organic syntheses, particularly in the production of small-molecule therapeutics.

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