CAS 2096331-99-4
:B-(2,5-Difluoro-4-propoxyphenyl)boronic acid
Description:
B-(2,5-Difluoro-4-propoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with two fluorine atoms and a propoxy group. This compound typically exhibits properties such as moderate solubility in organic solvents and potential reactivity with various electrophiles due to the boronic acid moiety, which can participate in Suzuki coupling reactions, making it valuable in organic synthesis and materials science. The presence of fluorine atoms often enhances the compound's stability and alters its electronic properties, while the propoxy group can influence its solubility and interaction with biological systems. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications. Overall, B-(2,5-Difluoro-4-propoxyphenyl)boronic acid is a versatile compound with applications in medicinal chemistry, organic synthesis, and materials development.
Formula:C9H11BF2O3
InChI:InChI=1S/C9H11BF2O3/c1-2-3-15-9-5-7(11)6(10(13)14)4-8(9)12/h4-5,13-14H,2-3H2,1H3
InChI key:InChIKey=OQIRUCQCCFOTJM-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C=C(OCCC)C(F)=C1
Synonyms:- Boronic acid, B-(2,5-difluoro-4-propoxyphenyl)-
- B-(2,5-Difluoro-4-propoxyphenyl)boronic acid
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