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Structure of 152367-89-0
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2-Amino-4-fluorobenzaldehyde features a strategically positioned amino group and fluorine atom on the aromatic ring, enabling enhanced reactivity in coupling reactions. This electron-rich scaffold facilitates efficient incorporation into pharmaceutical intermediates and functional materials, offering improved solubility and stability under standard conditions.
2-Amino-4-fluorobenzaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted heterocycles and biologically active scaffolds. Its ortho-amino and fluoro substituents provide complementary reactivity for palladium-catalyzed couplings, electrophilic aromatic substitutions, and condensation reactions. The aldehyde functionality facilitates facile derivatization via imine formation or reductive amination, while the molecule exhibits good bench stability and compatibility with common protecting groups.
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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: