4-(Trifluoromethyl)piperidin-4-ol

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Reagent Code: #242729
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CAS Number 373603-69-1

science Other reagents with same CAS 373603-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.14 g/mol
Formula C₆H₁₀F₃NO
badge Registry Numbers
MDL Number MFCD13179174
thermostat Physical Properties
Boiling Point 175.1±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of compounds with activity as antidepressants, antipsychotics, and analgesics. The presence of both hydroxyl and trifluoromethyl groups allows for selective modifications, enhancing drug potency and metabolic stability. Commonly employed in medicinal chemistry for building blocks in nitrogen-containing heterocycles. Also utilized in the design of receptor ligands due to its favorable conformational and electronic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,460.00
inventory 1g
10-20 days ฿5,300.00
inventory 10g
10-20 days ฿37,670.00
inventory 5g
10-20 days ฿20,230.00

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4-(Trifluoromethyl)piperidin-4-ol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of compounds with activity as antidepressants, antipsychotics, and analgesics. The presence of both hydroxyl and trifluoromethyl groups allows for selective modifications, enhancing drug potency and metabolic stability. Commonly employed in medicinal chemistry for building blocks in nitrogen-containing heterocycles. Also utilized in th

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of compounds with activity as antidepressants, antipsychotics, and analgesics. The presence of both hydroxyl and trifluoromethyl groups allows for selective modifications, enhancing drug potency and metabolic stability. Commonly employed in medicinal chemistry for building blocks in nitrogen-containing heterocycles. Also utilized in the design of receptor ligands due to its favorable conformational and electronic properties.

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