2-(N-Boc-aminomethyl)--5-(trifluoromethyl)pyridine

≥95%

Reagent Code: #216921
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CAS Number 1216276-20-8

science Other reagents with same CAS 1216276-20-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.25 g/mol
Formula C₁₂H₁₅F₃N₂O₂
badge Registry Numbers
MDL Number MFCD13187674
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Widely used in pharmaceutical synthesis, this compound serves as a key intermediate in the preparation of bioactive molecules, particularly kinase inhibitors and CNS-active agents. The presence of the Boc-protected amine allows for selective deprotection and further amine derivatization, enabling efficient coupling in multi-step reactions. The pyridine ring with a trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving pharmacokinetic properties. It is commonly employed in medicinal chemistry for constructing libraries in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,980.00
inventory 1g
10-20 days ฿8,880.00

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2-(N-Boc-aminomethyl)--5-(trifluoromethyl)pyridine
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Widely used in pharmaceutical synthesis, this compound serves as a key intermediate in the preparation of bioactive molecules, particularly kinase inhibitors and CNS-active agents. The presence of the Boc-protected amine allows for selective deprotection and further amine derivatization, enabling efficient coupling in multi-step reactions. The pyridine ring with a trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving pharmacokinetic properti

Widely used in pharmaceutical synthesis, this compound serves as a key intermediate in the preparation of bioactive molecules, particularly kinase inhibitors and CNS-active agents. The presence of the Boc-protected amine allows for selective deprotection and further amine derivatization, enabling efficient coupling in multi-step reactions. The pyridine ring with a trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving pharmacokinetic properties. It is commonly employed in medicinal chemistry for constructing libraries in structure-activity relationship (SAR) studies.

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