methyl4-bromo-6-((tert-butoxycarbonyl)amino)picolinate

≥95%

Reagent Code: #87755
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CAS Number 885326-87-4

science Other reagents with same CAS 885326-87-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.16 g/mol
Formula C₁₂H₁₅BrN₂O₄
badge Registry Numbers
MDL Number MFCD11226180
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the preparation of complex molecules, especially those involving picolinate derivatives. Its bromo and tert-butoxycarbonyl (Boc) protected amino groups make it a versatile building block for constructing more elaborate structures. The Boc group allows for selective deprotection, enabling further functionalization, while the bromo substituent facilitates cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in drug discovery. Additionally, its picolinate moiety is often utilized in chelating agents or metal coordination studies, making it valuable in materials science and catalysis research.

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inventory 1g
10-20 days ฿42,327.00
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methyl4-bromo-6-((tert-butoxycarbonyl)amino)picolinate
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This chemical is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the preparation of complex molecules, especially those involving picolinate derivatives. Its bromo and tert-butoxycarbonyl (Boc) protected amino groups make it a versatile building block for constructing more elaborate structures. The Boc group allows for selective deprotection, enabling further functionalization, while the bromo substituent facili

This chemical is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the preparation of complex molecules, especially those involving picolinate derivatives. Its bromo and tert-butoxycarbonyl (Boc) protected amino groups make it a versatile building block for constructing more elaborate structures. The Boc group allows for selective deprotection, enabling further functionalization, while the bromo substituent facilitates cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in drug discovery. Additionally, its picolinate moiety is often utilized in chelating agents or metal coordination studies, making it valuable in materials science and catalysis research.

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