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CAS 870718-01-7

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B-[3-Bromo-5-methyl-2-(1-methylethoxy)phenyl]boronic acid

Description:
B-[3-Bromo-5-methyl-2-(1-methylethoxy)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 bromine atom and a methyl group on the aromatic ring, which can influence its reactivity and solubility. The presence of the 1-methylethoxy group enhances its lipophilicity, potentially affecting its biological activity and interaction with other molecules. Boronic acids are typically used in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the compound may exhibit properties such as moderate stability under ambient conditions, but it can be sensitive to moisture and air, necessitating careful handling and storage. Overall, this compound represents a versatile building block in the field of synthetic organic chemistry.
Formula:C10H14BBrO3
InChI:InChI=1S/C10H14BBrO3/c1-6(2)15-10-8(11(13)14)4-7(3)5-9(10)12/h4-6,13-14H,1-3H3
InChI key:InChIKey=VTDMHYFQQWORBC-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=C(B(O)O)C=C(C)C=C1Br
Synonyms:
  • Boronic acid, B-[3-bromo-5-methyl-2-(1-methylethoxy)phenyl]-
  • Boronic acid, [3-bromo-5-methyl-2-(1-methylethoxy)phenyl]-
  • B-[3-Bromo-5-methyl-2-(1-methylethoxy)phenyl]boronic acid
  • (3-Bromo-2-isopropoxy-5-methylphenyl)boronic acid
  • 3-Bromo-2-isopropoxy-5-methylphenylboronic acid
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