1,1-dimethylethyl 2-[(methyloxy)methyl]-1-piperidinecarboxylate

≥98%

Reagent Code: #174116
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CAS Number 1351094-46-6

science Other reagents with same CAS 1351094-46-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.32 g/mol
Formula C₁₂H₂₃NO₃
thermostat Physical Properties
Boiling Point 287.9 °C
inventory_2 Storage & Handling
Density 1.003g/mL
Storage 2-8°C

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where protected piperidine derivatives are required. The 1,1-dimethylethyl (Boc) group serves as a protecting group for the piperidine nitrogen, enabling selective reactions at other sites in the molecule, while the 2-(methoxymethyl) substituent adds specific functionality to the piperidine ring. This compound is valuable in multi-step organic syntheses, especially in the preparation of central nervous system agents, receptor agonists, or antagonists. Its stability under various reaction conditions makes it suitable for use in industrial-scale processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿720.00
inventory 1g
10-20 days ฿2,000.00
inventory 5g
10-20 days ฿7,130.00

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1,1-dimethylethyl 2-[(methyloxy)methyl]-1-piperidinecarboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where protected piperidine derivatives are required. The 1,1-dimethylethyl (Boc) group serves as a protecting group for the piperidine nitrogen, enabling selective reactions at other sites in the molecule, while the 2-(methoxymethyl) substituent adds specific functionality to the piperidine ring. This compound is valuable in multi-step organic syntheses, especially in the prepa

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where protected piperidine derivatives are required. The 1,1-dimethylethyl (Boc) group serves as a protecting group for the piperidine nitrogen, enabling selective reactions at other sites in the molecule, while the 2-(methoxymethyl) substituent adds specific functionality to the piperidine ring. This compound is valuable in multi-step organic syntheses, especially in the preparation of central nervous system agents, receptor agonists, or antagonists. Its stability under various reaction conditions makes it suitable for use in industrial-scale processes.

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