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CAS 1256346-10-7

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B-[2-Chloro-5-(phenylmethoxy)phenyl]boronic acid

Description:
B-[2-Chloro-5-(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, particularly in Suzuki coupling reactions. The compound features a chloro substituent and a phenylmethoxy group, which contribute to its overall reactivity and solubility properties. Typically, boronic acids exhibit moderate stability under ambient conditions but can be sensitive to moisture and air, necessitating careful handling and storage. This compound may be utilized in organic synthesis, medicinal chemistry, and materials science, particularly in the development of pharmaceuticals and agrochemicals. Its unique structural features allow for potential applications in targeted drug delivery and as intermediates in the synthesis of more complex molecules. As with many boronic acids, it is important to consider its environmental impact and toxicity, ensuring proper safety protocols are followed during its use in laboratory settings.
Formula:C13H12BClO3
InChI:InChI=1S/C13H12BClO3/c15-13-7-6-11(8-12(13)14(16)17)18-9-10-4-2-1-3-5-10/h1-8,16-17H,9H2
InChI key:InChIKey=OABFVTYDVHFWDQ-UHFFFAOYSA-N
SMILES:O(CC1=CC=CC=C1)C2=CC(B(O)O)=C(Cl)C=C2
Synonyms:
  • Boronic acid, B-[2-chloro-5-(phenylmethoxy)phenyl]-
  • B-[2-Chloro-5-(phenylmethoxy)phenyl]boronic acid
  • [5-(Benzyloxy)-2-chlorophenyl]boronic acid
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