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CAS 1256355-51-7

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B-[2-Chloro-6-(methoxymethoxy)phenyl]boronic acid

Description:
B-[2-Chloro-6-(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 applications, including organic synthesis and medicinal chemistry. The compound features a chloro substituent and a methoxymethoxy group on a phenyl ring, contributing to its unique reactivity and solubility properties. Typically, boronic acids are utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. The presence of the methoxymethoxy group may enhance the compound's solubility in organic solvents and influence its electronic properties. Additionally, the chlorine atom can serve as a leaving group in nucleophilic substitution reactions. Overall, this compound's structural characteristics suggest potential utility in the development of pharmaceuticals and agrochemicals, as well as in materials science for creating functionalized polymers or other advanced materials.
Formula:C8H10BClO4
InChI:InChI=1S/C8H10BClO4/c1-13-5-14-7-4-2-3-6(10)8(7)9(11)12/h2-4,11-12H,5H2,1H3
InChI key:InChIKey=NGIKGLQZWMHUKA-UHFFFAOYSA-N
SMILES:O(COC)C1=C(B(O)O)C(Cl)=CC=C1
Synonyms:
  • Boronic acid, B-[2-chloro-6-(methoxymethoxy)phenyl]-
  • B-[2-Chloro-6-(methoxymethoxy)phenyl]boronic acid
  • 2-Chloro-6-(MethoxyMethoxy)phenylboronic acid
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