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Structure of 2894-45-3
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This aryl ketone features a strategically positioned amine and chlorophenyl group, enabling direct incorporation into bioactive scaffolds. The ortho-aminobenzoyl motif facilitates metal coordination and hydrogen bonding in catalytic systems, while the chlorophenyl moiety enhances lipophilicity and electron-withdrawing character. Designed for synthetic versatility, it integrates readily into pharmaceutical intermediates and functional materials under standard conditions.
(2-Aminophenyl)(2-chlorophenyl)methanone serves as a versatile building block in medicinal chemistry, enabling the construction of fused heterocyclic scaffolds through facile cyclization reactions. Its ortho-amino and chlorophenyl groups facilitate directed metalation and subsequent coupling processes, offering robust access to bioactive core structures. The compound exhibits good bench stability and compatibility with standard purification methods, making it well-suited for iterative synthetic workflows in API 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: