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Structure of 1685-19-4
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1-(2-Amino-5-chlorophenyl)ethanone features a chlorinated aromatic ring paired with an amino group and a ketone functionality, enabling direct integration into pharmaceutical intermediates. The electron-rich amine facilitates coupling reactions, while the para-chloro substituent enhances reactivity in electrophilic transformations. This compound serves as a key scaffold for targeted synthesis in medicinal chemistry applications.
1-(2-Amino-5-chlorophenyl)ethanone serves as a key building block in the synthesis of heterocyclic scaffolds and pharmaceutical intermediates. Its ortho-amino and chloro substituents enable diverse coupling reactions and cyclization pathways, while the acetyl group offers a handle for further functionalization. The compound exhibits good bench stability and facilitates efficient purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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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: