CAS 1016228-01-5
:1-(6-Bromo-3-fluoro-pyridin-2-yl)-ethanone
Description:
1-(6-Bromo-3-fluoro-pyridin-2-yl)-ethanone, with the CAS number 1016228-01-5, is a chemical compound characterized by its pyridine ring, which is substituted with both a bromine and a fluorine atom. The presence of these halogens contributes to its reactivity and potential applications in various chemical reactions. The ethanone functional group indicates that it contains a carbonyl (C=O) group adjacent to an ethyl group, which can influence its chemical behavior, particularly in nucleophilic addition reactions. This compound may exhibit polar characteristics due to the electronegative halogens, affecting its solubility in different solvents. Additionally, the bromine and fluorine substituents can enhance the compound's biological activity, making it of interest in medicinal chemistry and drug development. Overall, 1-(6-Bromo-3-fluoro-pyridin-2-yl)-ethanone is a versatile compound with potential applications in synthetic organic chemistry and pharmaceuticals.
Formula:C7H5BrFNO
InChI:InChI=1S/C7H5BrFNO/c1-4(11)7-5(9)2-3-6(8)10-7/h2-3H,1H3
InChI key:MXBFVOYREPRONK-UHFFFAOYSA-N
SMILES:CC(=O)C1=C(C=CC(=N1)Br)F
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1-(6-Bromo-3-fluoropyridin-2-yl)ethanone
CAS:1-(6-Bromo-3-fluoropyridin-2-yl)ethanoneFormula:C7H5BrFNOPurity:≥95%Molecular weight:218.0231Ethanone, 1-(6-bromo-3-fluoro-2-pyridinyl)-
CAS:Formula:C7H5BrFNOPurity:97%Color and Shape:SolidMolecular weight:218.02311-(6-Bromo-3-fluoropyridin-2-yl)ethan-1-one
CAS:Versatile small molecule scaffoldFormula:C7H5BrFNOPurity:Min. 95%Molecular weight:218.02 g/mol
