tert-butyl 4-(2-chlorophenoxy)piperidine-1-carboxylate

95%

Reagent Code: #242513
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CAS Number 552868-10-7

science Other reagents with same CAS 552868-10-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.8 g/mol
Formula C₁₆H₂₂ClNO₃
thermostat Physical Properties
Boiling Point 400.8±35.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.171 g/cm3
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of a piperidine ring and a chlorophenoxy group, which are common in neuroactive drugs. Commonly employed in research settings to design analogs for serotonin or dopamine receptor modulators. Also utilized in agrochemical research for developing new active ingredients with potential pesticidal or herbicidal activity. The tert-butyl carbamate (Boc) group allows for selective protection during multi-step organic syntheses, making it valuable in medicinal chemistry workflows.

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inventory 10g
10-20 days ฿98,230.00

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tert-butyl 4-(2-chlorophenoxy)piperidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of a piperidine ring and a chlorophenoxy group, which are common in neuroactive drugs. Commonly employed in research settings to design analogs for serotonin or dopamine receptor modulators. Also utilized in agrochemical research for developing new active ingredients with potential pesticidal

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules due to the presence of a piperidine ring and a chlorophenoxy group, which are common in neuroactive drugs. Commonly employed in research settings to design analogs for serotonin or dopamine receptor modulators. Also utilized in agrochemical research for developing new active ingredients with potential pesticidal or herbicidal activity. The tert-butyl carbamate (Boc) group allows for selective protection during multi-step organic syntheses, making it valuable in medicinal chemistry workflows.

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