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Structure of 35144-22-0
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4,6-Dimethyl-2-methylsulfonylpyrimidine features a pyrimidine core functionalized with two methyl groups at positions 4 and 6, and a methylsulfonyl group at position 2. This electron-deficient heterocycle serves as a stable, bench-compatible scaffold for constructing bioactive molecules in medicinal chemistry and agrochemical research.
4,6-Dimethyl-2-methylsulfonylpyrimidine serves as a versatile pyrimidine scaffold for medicinal chemistry and materials science applications. The methylsulfonyl group enhances solubility and metabolic stability, while the 4,6-dimethyl substitution provides steric protection and electronic modulation. This compound facilitates nucleophilic substitution reactions and functions as a key building block in the synthesis of kinase inhibitors and functionalized heterocycles. Its bench-stable nature and compatibility with standard coupling protocols support efficient route development and scale-up.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: