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Structure of 1260838-76-3
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(4-Amino-2,6-difluorophenyl)methanol features a benzene ring bearing electron-rich amino and sterically accessible difluoro substituents, enabling direct incorporation into bioactive scaffolds. The primary alcohol facilitates derivatization under standard conditions, while the para-amino group enhances solubility and reactivity in synthetic sequences.
(4-Amino-2,6-difluorophenyl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated aromatic scaffolds. Its primary alcohol functionality facilitates straightforward derivatization via esterification, etherification, or coupling reactions, while the ortho-fluoro substituents enhance metabolic stability and modulate electronic properties. The amine group provides additional handles for conjugation or further functionalization, offering synthetic flexibility in the construction of bioactive molecules.
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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: