tert-Butyl 6-bromopicolinate

96%

Reagent Code: #150555
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CAS Number 910044-07-4

science Other reagents with same CAS 910044-07-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.11 g/mol
Formula C₁₀H₁₂BrNO₂
badge Registry Numbers
MDL Number MFCD16036506
inventory_2 Storage & Handling
Storage 2-8°C, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active molecules. Its bromine functionality allows for further cross-coupling reactions, such as Suzuki or Heck couplings, enabling the introduction of aromatic or heteroaromatic systems. The tert-butyl ester group offers stability during multi-step syntheses and can be easily deprotected under acidic conditions to yield the corresponding carboxylic acid for further derivatization. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds with targeted biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,970.00
inventory 1g
10-20 days ฿4,600.00
inventory 5g
10-20 days ฿14,370.00

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tert-Butyl 6-bromopicolinate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active molecules. Its bromine functionality allows for further cross-coupling reactions, such as Suzuki or Heck couplings, enabling the introduction of aromatic or heteroaromatic systems. The tert-butyl ester group offers stability during multi-step syntheses and can be easily deprotected under acidic conditions to yield the corresponding carboxylic

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active molecules. Its bromine functionality allows for further cross-coupling reactions, such as Suzuki or Heck couplings, enabling the introduction of aromatic or heteroaromatic systems. The tert-butyl ester group offers stability during multi-step syntheses and can be easily deprotected under acidic conditions to yield the corresponding carboxylic acid for further derivatization. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds with targeted biological activity.

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