2-Amino-5-bromoisonicotinic acid

97%

Reagent Code: #135213
label
Alias 2-amino-5-bromoisonicolic acid; 2-amino-5-bromo-4-carboxylic acid; 2-amino-5-bromo-4-carboxylic acid pyridine
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CAS Number 1000339-23-0

science Other reagents with same CAS 1000339-23-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.0201 g/mol
Formula C₆H₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD09878357
inventory_2 Storage & Handling
Density 1.909
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug discovery. Commonly employed in organic synthesis for cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon and carbon-nitrogen bonds. Also serves as a building block in the preparation of agrochemicals and functional materials where substituted pyridines are required.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,290.00
inventory 5g
10-20 days ฿4,360.00
inventory 25g
10-20 days ฿16,310.00

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2-Amino-5-bromoisonicotinic acid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug discovery. Commonly employed in organic synthesis for cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon and carbon-nitrogen bonds. Also serves as a building block in the preparation of agrochemicals and functio

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drug discovery. Commonly employed in organic synthesis for cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon and carbon-nitrogen bonds. Also serves as a building block in the preparation of agrochemicals and functional materials where substituted pyridines are required.

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