6-(((Tert-butoxycarbonyl)amino)methyl)picolinic acid

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Reagent Code: #86825
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CAS Number 171670-07-8

science Other reagents with same CAS 171670-07-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.27 g/mol
Formula C₁₂H₁₆N₂O₄
badge Registry Numbers
MDL Number MFCD06657528
inventory_2 Storage & Handling
Storage room temperature, inert gas storage

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly in the synthesis of peptidomimetics and small-molecule inhibitors. Its structure, featuring both a picolinic acid moiety and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable for constructing complex molecules with specific functional groups. The Boc group can be selectively deprotected under mild acidic conditions, allowing for further modifications in multi-step synthetic routes. Additionally, it is employed in the preparation of ligands for metal coordination studies, owing to the chelating properties of the picolinic acid component. Its applications extend to medicinal chemistry, where it is used to design compounds targeting enzymes or receptors involved in disease pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,665.00
inventory 250mg
10-20 days ฿17,685.00
inventory 1g
10-20 days ฿36,450.00
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6-(((Tert-butoxycarbonyl)amino)methyl)picolinic acid
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly in the synthesis of peptidomimetics and small-molecule inhibitors. Its structure, featuring both a picolinic acid moiety and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable for constructing complex molecules with specific functional groups. The Boc group can be selectively deprotected under mild acidic conditio

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive molecules, particularly in the synthesis of peptidomimetics and small-molecule inhibitors. Its structure, featuring both a picolinic acid moiety and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable for constructing complex molecules with specific functional groups. The Boc group can be selectively deprotected under mild acidic conditions, allowing for further modifications in multi-step synthetic routes. Additionally, it is employed in the preparation of ligands for metal coordination studies, owing to the chelating properties of the picolinic acid component. Its applications extend to medicinal chemistry, where it is used to design compounds targeting enzymes or receptors involved in disease pathways.

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