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Structure of 1005-38-5
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4-Amino-6-chloro-2-(methylthio)pyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, featuring a chlorine atom at C6 and a methylthio group at C2 that enhance reactivity and metabolic stability. The amino functionality enables facile derivatization, while the electron-deficient pyrimidine ring facilitates nucleophilic substitution reactions under mild conditions. This compound is particularly valuable for constructing bioactive molecules in antiviral and anticancer research.
4-Amino-6-chloro-2-(methylthio)pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of pyrimidine-based scaffolds. Its amino and chloro groups facilitate nucleophilic substitution and coupling reactions, while the methylthio group offers orthogonal reactivity. The compound exhibits good bench stability and ease of purification, making it well-suited for medicinal chemistry 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-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: