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CAS 871125-81-4

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

Description:
B-[3-Bromo-5-(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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a bromine atom and an isopropoxy group attached to a phenyl ring, contributing to its reactivity and solubility properties. Typically, boronic acids are polar and can exhibit moderate solubility in polar solvents, while their reactivity can be influenced by the substituents on the aromatic ring. This specific compound may be utilized in organic synthesis, medicinal chemistry, and materials science due to its potential in forming complex molecular architectures. Additionally, the presence of the bromine atom can facilitate further functionalization, making it a versatile intermediate in synthetic pathways. As with many boronic acids, it is important to handle this compound with care, considering its potential reactivity and the need for proper storage conditions to maintain stability.
Formula:C9H12BBrO3
InChI:InChI=1S/C9H12BBrO3/c1-6(2)14-9-4-7(10(12)13)3-8(11)5-9/h3-6,12-13H,1-2H3
InChI key:InChIKey=OYCQIPZXNTZLQQ-UHFFFAOYSA-N
SMILES:O(C(C)C)C1=CC(B(O)O)=CC(Br)=C1
Synonyms:
  • Boronic acid, [3-bromo-5-(1-methylethoxy)phenyl]-
  • B-[3-Bromo-5-(1-methylethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-bromo-5-(1-methylethoxy)phenyl]-
  • (3-Bromo-5-isopropoxyphenyl)boronic acid
  • [3-Bromo-5-(propan-2-yloxy)phenyl]boronic acid
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