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Structure of 615-66-7
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2-Chlorobenzene-1,4-diamine features two amino groups positioned para to each other on a chlorinated benzene ring, enabling strategic integration into pharmaceutical intermediates and functional materials. The electron-rich aromatic core facilitates coupling reactions, while the chlorine atom provides a site for selective substitution. This compound serves as a key scaffold in agrochemical and dye synthesis due to its balanced reactivity and stability under standard conditions.
2-Chlorobenzene-1,4-diamine serves as a versatile building block in medicinal chemistry and materials science, enabling the synthesis of heterocyclic scaffolds via coupling reactions and cyclization processes. Its ortho-chloro substituent facilitates selective functionalization, while the diamine motif offers robust reactivity in amide, urea, and imine formation. Bench-stable and readily purified by recrystallization, it functions efficiently in standard synthetic workflows for API intermediates and functionalized aromatic systems.
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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: