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CAS 2121514-53-0

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B-[2,6-Dichloro-4-(hydroxymethyl)phenyl]boronic acid

Description:
B-[2,6-Dichloro-4-(hydroxymethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with dichloro and hydroxymethyl groups. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar solvents due to the hydroxymethyl group. The presence of the boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. The dichloro substituents can influence the electronic properties of the phenyl ring, potentially affecting reactivity and interactions with biological targets. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug design. Overall, this compound's unique structural features contribute to its utility in research and development within the fields of chemistry and pharmaceuticals.
Formula:C7H7BCl2O3
InChI:InChI=1S/C7H7BCl2O3/c9-5-1-4(3-11)2-6(10)7(5)8(12)13/h1-2,11-13H,3H2
InChI key:InChIKey=NZDFOFXGUWPQFO-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C=C(CO)C=C1Cl
Synonyms:
  • B-[2,6-Dichloro-4-(hydroxymethyl)phenyl]boronic acid
  • Boronic acid, B-[2,6-dichloro-4-(hydroxymethyl)phenyl]-
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