2-(1-((Benzyloxy)carbonyl)piperidin-4-yl)acetic acid

95%

Reagent Code: #146030
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CAS Number 63845-28-3

science Other reagents with same CAS 63845-28-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.32 g/mol
Formula C₁₅H₁₉NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring protected functional groups. Its structure allows for selective modification in multi-step organic syntheses, especially in the preparation of nitrogen-containing heterocyclic drugs. Commonly employed in medicinal chemistry for constructing peptidomimetics and CNS-targeted agents due to the piperidine backbone. The benzyloxycarbonyl (Cbz) protecting group facilitates controlled deprotection under mild conditions, making it valuable in solid-phase and solution-phase peptide coupling strategies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿450.00
inventory 5g
10-20 days ฿2,230.00
inventory 10g
10-20 days ฿4,180.00

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2-(1-((Benzyloxy)carbonyl)piperidin-4-yl)acetic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring protected functional groups. Its structure allows for selective modification in multi-step organic syntheses, especially in the preparation of nitrogen-containing heterocyclic drugs. Commonly employed in medicinal chemistry for constructing peptidomimetics and CNS-targeted agents due to the piperidine backbone. The benzyloxycarbonyl (Cbz) protecting g

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) requiring protected functional groups. Its structure allows for selective modification in multi-step organic syntheses, especially in the preparation of nitrogen-containing heterocyclic drugs. Commonly employed in medicinal chemistry for constructing peptidomimetics and CNS-targeted agents due to the piperidine backbone. The benzyloxycarbonyl (Cbz) protecting group facilitates controlled deprotection under mild conditions, making it valuable in solid-phase and solution-phase peptide coupling strategies.

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