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Structure of 1005-39-6
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2-(Methylthio)pyrimidine-4,6-diamine features a pyrimidine core functionalized with methylthio and diamine groups, enabling direct incorporation into heterocyclic scaffolds. The electron-rich diaminopyrimidine moiety facilitates efficient coupling reactions, while the methylthio substituent enhances solubility and stability under standard conditions. This compound serves as a key intermediate in the synthesis of bioactive nitrogen-containing molecules.
2-(Methylthio)pyrimidine-4,6-diamine serves as a versatile building block in heterocyclic synthesis, enabling the construction of pyrimidine-based scaffolds prevalent in medicinal chemistry. Its dual amine functionalities facilitate nucleophilic substitution and coupling reactions, while the methylthio group offers orthogonal reactivity for selective derivatization. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthetic campaigns and API intermediate development.
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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-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: