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CAS 850567-58-7

:

N-(4-Fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

Description:
N-(4-Fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide, with the CAS number 850567-58-7, is a chemical compound characterized by its unique structure that includes a fluorophenyl group and a dioxaborolane moiety. This compound typically exhibits properties associated with both aromatic and boron-containing compounds, which can influence its reactivity and solubility. The presence of the fluorine atom may enhance its lipophilicity and biological activity, making it of interest in medicinal chemistry. The dioxaborolane group is known for its ability to participate in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis. Additionally, this compound may exhibit specific interactions with biological targets, potentially leading to applications in drug development. Its stability, solubility, and reactivity can vary based on the solvent and conditions used, making it essential to consider these factors in practical applications. Overall, this compound represents a valuable structure in the field of organic and medicinal chemistry.
Formula:C19H21BFNO3
InChI:InChI=1S/C19H21BFNO3/c1-18(2)19(3,4)25-20(24-18)14-7-5-6-13(12-14)17(23)22-16-10-8-15(21)9-11-16/h5-12H,1-4H3,(H,22,23)
InChI key:InChIKey=SNPZVDHDRQNRNU-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(C(NC3=CC=C(F)C=C3)=O)=CC=C2
Synonyms:
  • N-(4-Fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
  • Benzamide, N-(4-fluorophenyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
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