1-(5-(Trifluoromethyl)pyridin-2-yl)piperidine-4-carboxylic acid

97%

Reagent Code: #240783
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CAS Number 406476-31-1

science Other reagents with same CAS 406476-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.24 g/mol
Formula C₁₂H₁₃F₃N₂O₂
thermostat Physical Properties
Melting Point 162°C
Boiling Point 420.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for treating inflammatory diseases and certain cancers. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Also employed in medicinal chemistry research to explore structure-activity relationships in pyridine-based drug candidates. The carboxylic acid group allows for easy derivatization, enabling the formation of amides and esters to optimize pharmacokinetic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿420.00
inventory 1g
10-20 days ฿640.00
inventory 5g
10-20 days ฿2,350.00
1-(5-(Trifluoromethyl)pyridin-2-yl)piperidine-4-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for treating inflammatory diseases and certain cancers. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Also employed in medicinal chemistry research to explore structure-activity relationships in pyridine-based drug candidates. The carboxylic acid group allows for easy derivatization, enabling the formation of amides and esters to optimi

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for treating inflammatory diseases and certain cancers. Its structure supports binding to specific enzyme targets, enhancing selectivity and potency. Also employed in medicinal chemistry research to explore structure-activity relationships in pyridine-based drug candidates. The carboxylic acid group allows for easy derivatization, enabling the formation of amides and esters to optimize pharmacokinetic properties.

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