2-Acetamido-5-bromoisonicotinic acid

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Reagent Code: #139071
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CAS Number 871269-03-3

science Other reagents with same CAS 871269-03-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.06 g/mol
Formula C₈H₇BrN₂O₃
badge Registry Numbers
MDL Number MFCD07363802
thermostat Physical Properties
Melting Point 258-262 °C
Boiling Point 569.9 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its bromo and carboxylic acid functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aromatic moieties. Also serves as a building block in the preparation of fluorescent probes and agrochemicals due to its stable pyridine core and derivatization potential.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿42,000.00

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2-Acetamido-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 bromo and carboxylic acid functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aromatic moieties. Also serves as a building block in the preparation of fluorescent probes and a

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors and other bioactive molecules. Its bromo and carboxylic acid functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce aromatic moieties. Also serves as a building block in the preparation of fluorescent probes and agrochemicals due to its stable pyridine core and derivatization potential.

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