CAS 913836-09-6
:(4-bromo-1-fluoro-2-naphthyl)boronic acid
Description:
(4-Bromo-1-fluoro-2-naphthyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene derivative. This compound features a naphthalene ring system substituted with a bromine atom at the 4-position and a fluorine atom at the 1-position, which can influence its reactivity and solubility. Boronic acids are known for their ability to form reversible complexes with diols, making them valuable in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. The presence of halogen substituents can enhance the electrophilicity of the naphthyl ring, potentially increasing its reactivity in various chemical transformations. Additionally, (4-bromo-1-fluoro-2-naphthyl)boronic acid may exhibit interesting properties such as fluorescence or changes in solubility based on pH due to the boronic acid group. Its unique structure and functional groups make it a useful intermediate in the synthesis of pharmaceuticals and agrochemicals.
Formula:C10H7BBrFO2
InChI:InChI=1/C10H7BBrFO2/c12-9-5-8(11(14)15)10(13)7-4-2-1-3-6(7)9/h1-5,14-15H
SMILES:c1ccc2c(c1)c(cc(c2F)B(O)O)Br
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Found 3 products.
4-BROMO-1-FLUORO-2-NAPHTHALENEBORONIC ACID
CAS:Formula:C10H7BBrFO2Purity:98%Color and Shape:SolidMolecular weight:268.87484-Bromo-1-fluoronaphthalene-2-boronic acid
CAS:4-Bromo-1-fluoronaphthalene-2-boronic acidFormula:C10H7BBrFO2Purity:98%Color and Shape: off white solidMolecular weight:268.87g/mol(4-Bromo-1-fluoronaphthalen-2-yl)boronic acid
CAS:Formula:C10H7BBrFO2Purity:98%Molecular weight:268.88


