tert-Butyl 6-[(1E)-2-[4-(4-fluorophenyl)-6-(1-methylethyl)-2-[methyl(methylsulfonyl)amino]-5-pyrimidinyl]ethenyl]-2,2-dimethyl-1,3-dioxane-4-acetate CAS:289042-12-2

The molecule features a tert-butyl ester group, which is a bulky protecting group that can be used to protect carboxylic acids or alcohols during chemical reactions. The presence of the tert-butyl group also increases the molecule's steric hindrance, which can affect its reactivity and stability. The molecule contains a pyrimidine ring, which is a six-membered heterocyclic ring with nitrogen atoms at positions 1, 3, and 5. The pyrimidine ring is a key structural component in many biologically active compounds, such as nucleotides and nucleic acids. The 5-position of the pyrimidine ring is substituted with a fluorophenyl group, which is an aryl group with a fluorine atom attached to it. Fluorine is a halogen atom, and its presence can influence the molecule's electronic properties and biological activity. The 2-position of the pyrimidine ring is substituted with a methyl(methylsulfonyl)amino group, which is a secondary amine with a methylsulfonyl group attached to it. This substituent can contribute to the molecule's overall solubility and may also play a role in its biological activity. The molecule contains an ethenyl group, which is a double bond between two carbon atoms. The ethenyl group is attached to the pyrimidine ring through a 1E configuration, which means that the double bond has a specific geometry that is consistent with the molecule's overall structure. Overall, this compound is likely to be of interest in the fields of medicinal chemistry and drug discovery due to its complex structure and the presence of various functional groups that offer potential for biological activity and synthetic utility.