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CAS 1256355-47-1

:

B-[3-Chloro-2-(methoxymethoxy)phenyl]boronic acid

Description:
B-[3-Chloro-2-(methoxymethoxy)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 chlorinated phenyl ring, which can influence its reactivity and solubility. The methoxymethoxy substituent enhances its solubility in organic solvents and may also affect its electronic properties. Boronic acids are typically used in organic synthesis, medicinal chemistry, and materials science due to their versatility. This specific compound may have applications in drug development or as a building block in the synthesis of more complex molecules. Its stability, reactivity, and solubility characteristics are essential for its practical applications in various chemical processes. As with many boronic acids, care should be taken in handling due to potential reactivity and the need for proper storage conditions to maintain its integrity.
Formula:C8H10BClO4
InChI:InChI=1S/C8H10BClO4/c1-13-5-14-8-6(9(11)12)3-2-4-7(8)10/h2-4,11-12H,5H2,1H3
InChI key:InChIKey=OPGUYLBIFIOJNR-UHFFFAOYSA-N
SMILES:O(COC)C1=C(B(O)O)C=CC=C1Cl
Synonyms:
  • B-[3-Chloro-2-(methoxymethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-chloro-2-(methoxymethoxy)phenyl]-
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