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Structure of 1700-02-3
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2,4-Dichloro-6-phenyl-1,3,5-triazine features a highly reactive triazine core with two chlorinated positions flanking a phenyl-substituted nitrogen. This electron-deficient heterocycle integrates readily into cross-coupling and nucleophilic substitution workflows, serving as a robust scaffold for constructing complex aromatic architectures under mild conditions.
2,4-Dichloro-6-phenyl-1,3,5-triazine serves as a versatile building block in synthetic organic chemistry, enabling the construction of functionalized triazine scaffolds through nucleophilic substitution. The dichloro functionality facilitates sequential coupling with amines, thiols, and other nucleophiles under mild conditions, offering high regioselectivity. Its phenyl-substituted core enhances stability and solubility, supporting efficient purification and scalability. This compound functions as a key intermediate in the development of pharmaceuticals, agrochemicals, and advanced materials.
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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: