4-Methoxypiperidine-1-carboxylic acid tert-butyl ester

≥98%

Reagent Code: #207753
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CAS Number 188622-27-7

science Other reagents with same CAS 188622-27-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.29 g/mol
Formula C₁₁H₂₁NO₃
thermostat Physical Properties
Boiling Point 274 °C
inventory_2 Storage & Handling
Density 1.03g/mL
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where the piperidine ring serves as a structural scaffold. The tert-butyl carbamate (Boc) protecting group allows for controlled functionalization of the nitrogen atom, making it valuable in multi-step organic synthesis. The 4-methoxy substituent can influence the polarity and conformation of the molecule, aiding in the modulation of biological activity or pharmacokinetic properties in drug candidates. Commonly employed in medicinal chemistry for the preparation of centrally acting agents, including those targeting neurological and psychiatric disorders.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿2,530.00
4-Methoxypiperidine-1-carboxylic acid tert-butyl ester
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where the piperidine ring serves as a structural scaffold. The tert-butyl carbamate (Boc) protecting group allows for controlled functionalization of the nitrogen atom, making it valuable in multi-step organic synthesis. The 4-methoxy substituent can influence the polarity and conformation of the molecule, aiding in the modulation of biological activity or pharmacokinet

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where the piperidine ring serves as a structural scaffold. The tert-butyl carbamate (Boc) protecting group allows for controlled functionalization of the nitrogen atom, making it valuable in multi-step organic synthesis. The 4-methoxy substituent can influence the polarity and conformation of the molecule, aiding in the modulation of biological activity or pharmacokinetic properties in drug candidates. Commonly employed in medicinal chemistry for the preparation of centrally acting agents, including those targeting neurological and psychiatric disorders.

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