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Structure of 30894-84-9
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2-Chloro-4,6-dimethyl-1,3,5-triazine serves as a reactive triazine derivative for nucleophilic substitution, enabling efficient functionalization in synthetic chemistry. The chloro group at the 2-position provides high electrophilicity, while the methyl substituents enhance stability and solubility. This compound integrates readily into heterocyclic frameworks under mild conditions.
2-Chloro-4,6-dimethyl-1,3,5-triazine serves as a versatile electrophilic building block in synthetic organic chemistry, enabling efficient C–N bond formation under mild conditions. Its reactivity is well-established in the construction of triazine-based heterocycles and pharmaceutical intermediates. The molecule exhibits excellent bench stability, facilitates straightforward purification, and demonstrates broad functional group tolerance in nucleophilic substitution reactions, making it a reliable reagent for medicinal chemistry and process development workflows.
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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: