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Structure of 2369-29-1
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3,5-Difluorobenzene-1,2-diamine features a symmetrically substituted aromatic core with two fluorine atoms at the 3 and 5 positions, enhancing electronic effects while maintaining stability. The ortho-diamine functionality enables direct incorporation into heterocyclic systems, offering high reactivity in transition metal-catalyzed coupling and cyclization reactions. This bench-stable derivative serves as a key building block for advanced pharmaceutical intermediates and functional materials.
3,5-Difluorobenzene-1,2-diamine serves as a versatile building block in medicinal chemistry and materials science, enabling the construction of fluorinated heterocycles via cyclization reactions. Its ortho-diamine functionality facilitates metal-catalyzed coupling processes and Schiff base formation, while the 3,5-difluoro substitution pattern enhances metabolic stability and modulates electronic properties. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis 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: