Ethyl N-Boc-4-methylpiperidine-4-carboxylate

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Reagent Code: #181843
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CAS Number 189442-87-3

science Other reagents with same CAS 189442-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.35 g/mol
Formula C₁₄H₂₅NO₄
badge Registry Numbers
MDL Number MFCD08689955
inventory_2 Storage & Handling
Density 1.0134
Storage Room temperature, dry

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a key intermediate in the production of active pharmaceutical ingredients (APIs), particularly those involving piperidine-based structures. Its N-Boc protection allows for selective reactivity at the nitrogen site, enabling controlled multi-step reactions without interference. The ester group can be easily hydrolyzed or transformed into amides, making it valuable for constructing complex drug molecules. Commonly applied in the development of central nervous system agents, including analgesics and psychiatric medications, due to the prevalence of 4-substituted piperidines in bioactive compounds. Its structural stability and compatibility with various reaction conditions enhance its utility in medicinal chemistry and process development.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,116.50
inventory 25g
10-20 days ฿8,920.00
inventory 1g
10-20 days ฿264.00
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Ethyl N-Boc-4-methylpiperidine-4-carboxylate
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Widely used in pharmaceutical synthesis, this compound serves as a key intermediate in the production of active pharmaceutical ingredients (APIs), particularly those involving piperidine-based structures. Its N-Boc protection allows for selective reactivity at the nitrogen site, enabling controlled multi-step reactions without interference. The ester group can be easily hydrolyzed or transformed into amides, making it valuable for constructing complex drug molecules. Commonly applied in the development o

Widely used in pharmaceutical synthesis, this compound serves as a key intermediate in the production of active pharmaceutical ingredients (APIs), particularly those involving piperidine-based structures. Its N-Boc protection allows for selective reactivity at the nitrogen site, enabling controlled multi-step reactions without interference. The ester group can be easily hydrolyzed or transformed into amides, making it valuable for constructing complex drug molecules. Commonly applied in the development of central nervous system agents, including analgesics and psychiatric medications, due to the prevalence of 4-substituted piperidines in bioactive compounds. Its structural stability and compatibility with various reaction conditions enhance its utility in medicinal chemistry and process development.

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