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CAS 957062-59-8

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B-[4-(4-Fluoro-2-nitrophenoxy)phenyl]boronic acid

Description:
B-[4-(4-Fluoro-2-nitrophenoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a 4-fluoro-2-nitrophenoxy group, contributing to its unique electronic properties and potential reactivity. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity, while the nitro group may serve as a site for further chemical modifications. This compound is typically used in the development of pharmaceuticals, particularly in the synthesis of biologically active molecules. Its boronic acid moiety also makes it a candidate for applications in materials science, such as in the creation of sensors or catalysts. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and potential environmental impact.
Formula:C12H9BFNO5
InChI:InChI=1S/C12H9BFNO5/c14-9-3-6-12(11(7-9)15(18)19)20-10-4-1-8(2-5-10)13(16)17/h1-7,16-17H
InChI key:InChIKey=SAOPFWUHFIYTSV-UHFFFAOYSA-N
SMILES:O(C1=C(N(=O)=O)C=C(F)C=C1)C2=CC=C(B(O)O)C=C2
Synonyms:
  • 4-(4-Fluoro-2-nitrophenoxy)phenylboronic acid
  • B-[4-(4-Fluoro-2-nitrophenoxy)phenyl]boronic acid
  • Boronic acid, B-[4-(4-fluoro-2-nitrophenoxy)phenyl]-
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