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CAS 1218790-59-0

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B-[3-Chloro-5-methoxy-4-(phenylmethoxy)phenyl]boronic acid

Description:
B-[3-Chloro-5-methoxy-4-(phenylmethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, including Suzuki coupling. The compound features a phenylmethoxy substituent and a chloro group, contributing to its reactivity and potential applications in organic synthesis and medicinal chemistry. The methoxy group enhances solubility and can influence the electronic properties of the molecule. This compound may exhibit properties such as moderate to high stability under standard conditions, and its boronic acid functionality allows for participation in cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the presence of chlorine and methoxy groups can affect its biological activity, making it a candidate for further investigation in drug development or as a building block in complex organic molecules. As with many boronic acids, it may also have applications in sensor technology and materials science.
Formula:C14H14BClO4
InChI:InChI=1S/C14H14BClO4/c1-19-13-8-11(15(17)18)7-12(16)14(13)20-9-10-5-3-2-4-6-10/h2-8,17-18H,9H2,1H3
InChI key:InChIKey=IFFSNNYWDSJWKE-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=C(OC)C=C(B(O)O)C=C2Cl
Synonyms:
  • Boronic acid, B-[3-chloro-5-methoxy-4-(phenylmethoxy)phenyl]-
  • B-[3-Chloro-5-methoxy-4-(phenylmethoxy)phenyl]boronic acid
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