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CAS 1256346-46-9

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B-[2,4-Dichloro-5-(2-methylpropoxy)phenyl]boronic acid

Description:
B-[2,4-Dichloro-5-(2-methylpropoxy)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. This compound features a phenyl ring substituted with two chlorine atoms and a branched alkoxy group, which contributes to its hydrophobic properties. The dichloro substitution enhances its reactivity and potential applications in cross-coupling reactions, particularly in the synthesis of complex organic molecules. Boronic acids are often utilized in medicinal chemistry and materials science due to their ability to participate in Suzuki-Miyaura coupling reactions, making this compound potentially valuable in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the 2-methylpropoxy group may influence its solubility and stability in various solvents. Overall, B-[2,4-Dichloro-5-(2-methylpropoxy)phenyl]boronic acid exhibits characteristics typical of boronic acids, including reactivity, functional versatility, and potential applications in organic synthesis.
Formula:C10H13BCl2O3
InChI:InChI=1S/C10H13BCl2O3/c1-6(2)5-16-10-3-7(11(14)15)8(12)4-9(10)13/h3-4,6,14-15H,5H2,1-2H3
InChI key:InChIKey=NIDCPTZXOXJCGW-UHFFFAOYSA-N
SMILES:O(CC(C)C)C1=CC(B(O)O)=C(Cl)C=C1Cl
Synonyms:
  • Boronic acid, B-[2,4-dichloro-5-(2-methylpropoxy)phenyl]-
  • B-[2,4-Dichloro-5-(2-methylpropoxy)phenyl]boronic acid
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