Ethyl N-Boc-piperidine-3-carboxylate

98%

Reagent Code: #181515
label
Alias Ethyl N-Boc-3-piperidinic acid; 1-(tert-butyl)3-ethyl 1,3-piperidinic acid 1-(tert-butoxycarbonyl)-piperidin-3-carboxylate ethyl N-Boc-DL-piperidinic acid
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CAS Number 130250-54-3

science Other reagents with same CAS 130250-54-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.33 g/mol
Formula C₁₃H₂₃NO₄
badge Registry Numbers
MDL Number MFCD04116274
thermostat Physical Properties
Melting Point 34℃ to 38℃
inventory_2 Storage & Handling
Storage 2~8 ℃

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where piperidine derivatives are required. Its Boc-protected amine group allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, including antidepressants and antipsychotics. Also utilized in the synthesis of agrochemicals and specialty chemicals requiring chiral piperidine scaffolds.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿480.00
inventory 100g
10-20 days ฿1,460.00
inventory 5g
10-20 days ฿144.00

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Ethyl N-Boc-piperidine-3-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where piperidine derivatives are required. Its Boc-protected amine group allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, including antidepressants and antipsychotics. Also utilized in the synthesis of agrochemicals
Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where piperidine derivatives are required. Its Boc-protected amine group allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, including antidepressants and antipsychotics. Also utilized in the synthesis of agrochemicals and specialty chemicals requiring chiral piperidine scaffolds.
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