tert-butyl3-(chloromethyl)piperidine-1-carboxylate

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Reagent Code: #243317
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CAS Number 876589-09-2

science Other reagents with same CAS 876589-09-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.735 g/mol
Formula C₁₁H₂₀ClNO₂
badge Registry Numbers
MDL Number MFCD09953348
thermostat Physical Properties
Boiling Point 303.2±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.076 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine rings. Its chloromethyl group allows for further alkylation or coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of central nervous system (CNS) agents, including antidepressants, antipsychotics, and cognitive enhancers. Also utilized in the creation of agrochemicals and specialty chemicals where a protected piperidine scaffold is needed. The tert-butyl carbamate (Boc) protection ensures stability during multi-step syntheses and allows for selective deprotection under mild acidic conditions.

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inventory 1g
10-20 days ฿35,300.00

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tert-butyl3-(chloromethyl)piperidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine rings. Its chloromethyl group allows for further alkylation or coupling reactions, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in the preparation of central nervous system (CNS) agents, including antidepressants, antipsychotics, and cognitive enhancers. Also utilized in the creation of agrochemicals and specialty chemicals where a protected piperidine scaffold is needed. The tert-butyl carbamate (Boc) protection ensures stability during multi-step syntheses and allows for selective deprotection under mild acidic conditions.
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