CAS 849035-86-5
:(3-ethoxy-2,6-difluorophenyl)boronic acid
Description:
(3-Ethoxy-2,6-difluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with an ethoxy group and two fluorine atoms. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity in cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura coupling reactions, which are widely used in the synthesis of pharmaceuticals and agrochemicals. The fluorine substituents can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in chemical reactions. Additionally, the ethoxy group may affect the compound's solubility and stability. Overall, (3-ethoxy-2,6-difluorophenyl)boronic acid is a versatile building block in synthetic organic chemistry, with applications in various fields, including medicinal chemistry and materials science.
Formula:C8H9BF2O3
InChI:InChI=1/C8H9BF2O3/c1-2-14-6-4-3-5(10)7(8(6)11)9(12)13/h3-4,12-13H,2H2,1H3
SMILES:CCOc1ccc(c(c1F)B(O)O)F
Synonyms:- 2,6-Difluoro-3-Ethoxybenzeneboronic Acid
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CAS:Ethyl 5-fluoro-7-(methylsulphonyl)-1H-indole-2-carboxylatePurity:≥95%Molecular weight:285.29g/mol
