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CAS 957198-29-7

:

4-[3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinyl]morpholine

Description:
4-[3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinyl]morpholine, with the CAS number 957198-29-7, is a synthetic organic compound characterized by its complex molecular structure, which includes a morpholine ring, a pyridine moiety, and a boron-containing dioxaborolane group. This compound is typically used in medicinal chemistry and drug development due to its potential biological activity and ability to interact with various biological targets. The presence of the fluorine atom enhances its lipophilicity and may influence its pharmacokinetic properties. The dioxaborolane group is notable for its role in facilitating chemical reactions, particularly in the context of boron chemistry, which is often utilized in the synthesis of pharmaceuticals. The compound's solubility, stability, and reactivity can be influenced by its functional groups, making it a subject of interest for further research in organic synthesis and medicinal applications. Overall, this compound exemplifies the intricate design often found in modern drug candidates.
Formula:C15H22BFN2O3
InChI:InChI=1S/C15H22BFN2O3/c1-14(2)15(3,4)22-16(21-14)11-5-6-18-13(12(11)17)19-7-9-20-10-8-19/h5-6H,7-10H2,1-4H3
InChI key:InChIKey=PRTVABCMQIBLAP-UHFFFAOYSA-N
SMILES:FC=1C(B2OC(C)(C)C(C)(C)O2)=CC=NC1N3CCOCC3
Synonyms:
  • 4-[3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinyl]morpholine
  • 4-[3-Fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridin-2-yl]morpholine
  • 3-Fluoro-2-(morpholino)pyridine-4-boronic acid pinacol ester
  • Morpholine, 4-[3-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinyl]-
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