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CAS 2096339-60-3

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B-(2-Chloro-3-methoxy-4-pyridinyl)boronic acid

Description:
B-(2-Chloro-3-methoxy-4-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and having moderate stability under standard laboratory conditions. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the chloro and methoxy substituents on the pyridine ring can influence its reactivity and biological activity, potentially enhancing its role as a pharmaceutical intermediate or in agrochemical applications. Additionally, the compound may exhibit specific interactions with biological targets, which can be explored for therapeutic purposes. As with many boronic acids, it is important to handle this substance with care, considering its potential reactivity and the need for appropriate safety measures in laboratory settings.
Formula:C6H7BClNO3
InChI:InChI=1S/C6H7BClNO3/c1-12-5-4(7(10)11)2-3-9-6(5)8/h2-3,10-11H,1H3
InChI key:InChIKey=LJJVKTFOWKKYPR-UHFFFAOYSA-N
SMILES:O(C)C=1C(B(O)O)=CC=NC1Cl
Synonyms:
  • Boronic acid, B-(2-chloro-3-methoxy-4-pyridinyl)-
  • B-(2-Chloro-3-methoxy-4-pyridinyl)boronic acid
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