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Structure of 1979-96-0
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4,6-Dichloro-2-(methylthio)-5-nitropyrimidine features a trifunctional core enabling direct coupling in heterocyclic synthesis. The electron-deficient pyrimidine ring pairs with reactive chlorine sites and a methylthio group, facilitating selective substitution under mild conditions. This scaffold delivers high reactivity in cross-coupling and nucleophilic displacement reactions, particularly valuable in medicinal chemistry and agrochemical development workflows.
4,6-Dichloro-2-(methylthio)-5-nitropyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyrimidine-based scaffolds. The dichloro substitution pattern facilitates sequential nucleophilic aromatic substitution, while the methylthio and nitro groups offer orthogonal reactivity for downstream functionalization. Bench-stable and compatible with standard purification methods, it supports scalable synthesis of heterocyclic intermediates.
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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: