4-(Trifluoromethyl)piperidine hydrochloride

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Reagent Code: #241019
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CAS Number 155849-49-3

science Other reagents with same CAS 155849-49-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.61 g/mol
Formula C₆H₁₀F₃N HCl
badge Registry Numbers
MDL Number MFCD04971993
thermostat Physical Properties
Melting Point 155-159°C
Boiling Point 167°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used in pharmaceutical synthesis as a key building block for active pharmaceutical ingredients (APIs), particularly in drugs targeting central nervous system disorders. Its structure enhances metabolic stability and bioavailability, making it valuable in the development of antidepressants, antipsychotics, and analgesics. Also employed in agrochemicals for the creation of novel pesticides due to the electron-withdrawing trifluoromethyl group improving compound resilience. Common in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,750.00

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4-(Trifluoromethyl)piperidine hydrochloride
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Used in pharmaceutical synthesis as a key building block for active pharmaceutical ingredients (APIs), particularly in drugs targeting central nervous system disorders. Its structure enhances metabolic stability and bioavailability, making it valuable in the development of antidepressants, antipsychotics, and analgesics. Also employed in agrochemicals for the creation of novel pesticides due to the electron-withdrawing trifluoromethyl group improving compound resilience. Common in medicinal chemistry for

Used in pharmaceutical synthesis as a key building block for active pharmaceutical ingredients (APIs), particularly in drugs targeting central nervous system disorders. Its structure enhances metabolic stability and bioavailability, making it valuable in the development of antidepressants, antipsychotics, and analgesics. Also employed in agrochemicals for the creation of novel pesticides due to the electron-withdrawing trifluoromethyl group improving compound resilience. Common in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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