tert-butyl 4-methoxy-4-phenylpiperidine-1-carboxylate

95%

Reagent Code: #238806
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CAS Number 201609-37-2

science Other reagents with same CAS 201609-37-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.39 g/mol
Formula C₁₇H₂₅NO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. Its structure supports the construction of complex piperidine-based molecules, which are common in central nervous system agents. The tert-butyl carbamate (Boc) group provides protection for the nitrogen during multi-step syntheses, allowing selective reactions at other functional sites. The 4-methoxy-4-phenyl substitution pattern adds steric bulk and polarity, influencing receptor binding characteristics in drug candidates. Commonly employed in medicinal chemistry for designing analogs of bioactive molecules, especially in the exploration of analgesics, antipsychotics, and antidepressants.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿20,000.00
tert-butyl 4-methoxy-4-phenylpiperidine-1-carboxylate
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. Its structure supports the construction of complex piperidine-based molecules, which are common in central nervous system agents. The tert-butyl carbamate (Boc) group provides protection for the nitrogen during multi-step syntheses, allowing selective reactions at other functional sites. The 4-methoxy-4-phenyl substitution pattern adds steric bulk and polarity, influencing receptor binding character

Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. Its structure supports the construction of complex piperidine-based molecules, which are common in central nervous system agents. The tert-butyl carbamate (Boc) group provides protection for the nitrogen during multi-step syntheses, allowing selective reactions at other functional sites. The 4-methoxy-4-phenyl substitution pattern adds steric bulk and polarity, influencing receptor binding characteristics in drug candidates. Commonly employed in medicinal chemistry for designing analogs of bioactive molecules, especially in the exploration of analgesics, antipsychotics, and antidepressants.

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