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CAS 158178-36-0

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3,4-DIFLUORO-5-NITROPHENYLBORONIC ACID

Description:
3,4-Difluoro-5-nitrophenylboronic 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 nitro group. This compound typically exhibits a solid state at room temperature and is soluble in polar organic solvents. The presence of the boronic acid group allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The fluorine substituents can influence the electronic properties of the molecule, potentially enhancing its reactivity and stability. Additionally, the nitro group serves as a strong electron-withdrawing group, which can further modulate the compound's reactivity. Overall, 3,4-difluoro-5-nitrophenylboronic acid is significant in medicinal chemistry and materials science, where it may be utilized in the development of pharmaceuticals and advanced materials. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C6H4BF2NO4
InChI:InChI=1/C6H4BF2NO4/c8-4-1-3(7(11)12)2-5(6(4)9)10(13)14/h1-2,11-12H
SMILES:c1c(cc(c(c1F)F)N(=O)=O)B(O)O
Synonyms:
  • (3,4-Difluoro-5-nitrophenyl)boronicacid
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