tert-Butyl 4-(Aminomethyl)-3-fluoropiperidine-1-carboxylate

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Reagent Code: #152399
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CAS Number 1303972-96-4

science Other reagents with same CAS 1303972-96-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.30 g/mol
Formula C₁₁H₂₁FN₂O₂
badge Registry Numbers
MDL Number MFCD18909804
thermostat Physical Properties
Boiling Point 307.4±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.09±0.1 g/cm3(Predicted)
Storage Room temperature, dry, light-proof

description Product Description

Used in pharmaceutical synthesis as a key intermediate for developing bioactive molecules, particularly in the production of central nervous system (CNS) agents. Its structure supports the creation of selective receptor modulators, including those targeting neurological disorders such as depression, anxiety, and psychosis. The presence of a protected amine group allows for controlled functionalization, making it valuable in medicinal chemistry for building complex piperidine-based drug candidates. Commonly employed in the development of serotonin and dopamine receptor ligands due to its favorable stereochemistry and fluorine substitution, which enhances metabolic stability and membrane permeability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿19,190.00
inventory 100mg
10-20 days ฿30,180.00
inventory 250mg
10-20 days ฿60,870.00

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tert-Butyl 4-(Aminomethyl)-3-fluoropiperidine-1-carboxylate
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Used in pharmaceutical synthesis as a key intermediate for developing bioactive molecules, particularly in the production of central nervous system (CNS) agents. Its structure supports the creation of selective receptor modulators, including those targeting neurological disorders such as depression, anxiety, and psychosis. The presence of a protected amine group allows for controlled functionalization, making it valuable in medicinal chemistry for building complex piperidine-based drug candidates. Commonly
Used in pharmaceutical synthesis as a key intermediate for developing bioactive molecules, particularly in the production of central nervous system (CNS) agents. Its structure supports the creation of selective receptor modulators, including those targeting neurological disorders such as depression, anxiety, and psychosis. The presence of a protected amine group allows for controlled functionalization, making it valuable in medicinal chemistry for building complex piperidine-based drug candidates. Commonly employed in the development of serotonin and dopamine receptor ligands due to its favorable stereochemistry and fluorine substitution, which enhances metabolic stability and membrane permeability.
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