CAS 1451393-49-9
:5-Borono-2-bromo-3-pyridinecarboxylic acid
Description:
5-Borono-2-bromo-3-pyridinecarboxylic acid is an organic compound characterized by its boronic acid functional group, which is known for its reactivity in cross-coupling reactions, particularly in the formation of carbon-carbon bonds. The presence of a bromine atom enhances its electrophilic properties, making it a useful intermediate in various synthetic applications. The pyridine ring contributes to the compound's aromaticity and can influence its solubility and reactivity. This compound is typically utilized in medicinal chemistry and materials science, particularly in the development of pharmaceuticals and agrochemicals. Its carboxylic acid group provides acidic properties, allowing for potential interactions with bases and metal ions. Additionally, the boron atom can participate in coordination chemistry, making it valuable in the synthesis of boron-containing compounds. Overall, 5-Borono-2-bromo-3-pyridinecarboxylic acid is a versatile building block in organic synthesis, with applications that leverage its unique structural features and reactivity.
Formula:C6H5BBrNO4
InChI:InChI=1S/C6H5BBrNO4/c8-5-4(6(10)11)1-3(2-9-5)7(12)13/h1-2,12-13H,(H,10,11)
InChI key:InChIKey=KFCCLRYBPPHKBI-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C=C(B(O)O)C=NC1Br
Synonyms:- 3-Pyridinecarboxylic acid, 5-borono-2-bromo-
- 5-Borono-2-bromo-3-pyridinecarboxylic acid
- 2-Bromo-3-carboxypyridine-5-boronic acid
- 5-Borono-2-bromo-pyridine-3-carboxylic acid
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