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Structure of 1973-04-2
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2,4-Dichloro-6-methyl-1,3,5-triazine serves as a reactive triazine core for nucleophilic substitution, enabling efficient coupling in heterocyclic synthesis. The methyl group enhances solubility and stability under standard conditions, while the dichloro substituents provide orthogonal reactivity for sequential functionalization. This compound integrates readily into advanced molecular architectures requiring precise placement of electron-deficient triazine units.
2,4-Dichloro-6-methyl-1,3,5-triazine serves as a versatile electrophilic building block in synthetic organic chemistry, enabling efficient construction of triazine-based heterocycles. Its dichloro substitution pattern facilitates selective nucleophilic displacement reactions, while the methyl group enhances solubility and stability under standard reaction conditions. This compound functions reliably in the synthesis of agrochemical intermediates and pharmaceutical scaffolds, offering predictable reactivity and straightforward purification.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2923
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Class : 8 (6.1)
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Packing Group : Ⅱ
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Hazard Statements : H302-H314-H317
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: