CAS 1072951-80-4
:B-(3-Bromo-5-formyl-2-methoxyphenyl)boronic acid
Description:
B-(3-Bromo-5-formyl-2-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic transformations, particularly in Suzuki coupling reactions. The compound features a bromine atom and a formyl group on a phenyl ring, contributing to its potential as a building block in organic synthesis. The methoxy group enhances its solubility and may influence its electronic properties, making it useful in medicinal chemistry and material science. The boronic acid moiety allows for the formation of stable complexes with diols, which is significant in applications such as sensing and drug delivery. Additionally, the presence of the formyl group suggests potential reactivity in further functionalization, enabling the synthesis of more complex molecules. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry, particularly in the development of pharmaceuticals and advanced materials.
Formula:C8H8BBrO4
InChI:InChI=1S/C8H8BBrO4/c1-14-8-6(9(12)13)2-5(4-11)3-7(8)10/h2-4,12-13H,1H3
InChI key:InChIKey=UUPRSFVSYMWVRC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OC)C(Br)=CC(C=O)=C1
Synonyms:- B-(3-Bromo-5-formyl-2-methoxyphenyl)boronic acid
- Boronic acid, B-(3-bromo-5-formyl-2-methoxyphenyl)-
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Found 3 products.
3-Bromo-5-formyl-2-methoxyphenylboronic acid
CAS:Formula:C8H8BBrO4Purity:96%Color and Shape:SolidMolecular weight:258.86173-Bromo-5-formyl-2-methoxyphenylboronic acid
CAS:<p>3-Bromo-5-formyl-2-methoxyphenylboronic acid</p>Purity:≥95%Molecular weight:258.86g/mol(3-Bromo-5-formyl-2-methoxyphenyl)boronic acid
CAS:Formula:C8H8BBrO4Purity:96%Molecular weight:258.86


