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Structure of 54198-72-0
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(4,6-Dimethylpyrimidin-2-yl)methanol features a pyrimidine core with methyl groups at the 4- and 6-positions, enhancing steric protection and electronic stability. The pendant hydroxymethyl group enables straightforward derivatization, facilitating integration into ligands, catalysts, or bioactive scaffolds under standard conditions.
(4,6-Dimethylpyrimidin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. Its benzylic alcohol functionality facilitates direct functionalization, including oxidation to carboxylic acids or conversion to esters and ethers, with excellent stability under standard synthetic conditions. The dimethyl substitution pattern enhances solubility and metabolic stability, while the pyrimidine core provides a robust platform for further derivatization in target-oriented synthesis.
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Lot numbers can be found on the outside label of a product: