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CAS 1217500-89-4

:

3-Chloro-2-isobutoxypyridine-5-boronicacid

Description:
3-Chloro-2-isobutoxypyridine-5-boronic acid is an organoboron compound characterized by the presence of a pyridine ring substituted with a chlorine atom and an isobutoxy group, along with a boronic acid functional group. This compound typically exhibits properties associated with both the pyridine and boronic acid functionalities, such as moderate solubility in polar organic solvents and potential reactivity with various electrophiles. The boronic acid moiety allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The presence of the chlorine atom can influence the compound's reactivity and stability, while the isobutoxy group may enhance solubility and steric hindrance. Overall, this compound is of interest in medicinal chemistry and materials science due to its potential applications in drug development and the synthesis of complex organic molecules. Safety data and handling precautions should be considered, as with all chemical substances, to ensure proper laboratory practices.
Formula:C9H13BClNO3
InChI:InChI=1S/C9H13BClNO3/c1-6(2)5-15-9-8(11)3-7(4-12-9)10(13)14/h3-4,6,13-14H,5H2,1-2H3
SMILES:CC(C)COc1c(cc(cn1)B(O)O)Cl
Synonyms:
  • (5-Chloro-6-isobutoxy-3-pyridinyl)boronic acid
  • 3-Chloro-2-isobutoxypyridine-5-boronic acid :
  • 5-Chloro-6-isobutoxypyridine-3-boronic acid
  • 5-chloro-6-(2-methylpropoxy)pyridin-3-yl]boronic acid
  • 5-Chloro-6-isobutoxypyridin-3-ylboronic acid
  • B-[5-Chloro-6-(2-methylpropoxy)-3-pyridinyl]boronic acid
  • Boronic acid, B-[5-chloro-6-(2-methylpropoxy)-3-pyridinyl]-
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