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Structure of 906811-49-2
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This bench-stable arylmethanol features a fluorinated aromatic ring paired with an ortho-amino group, enabling direct incorporation into bioactive scaffolds. The primary alcohol facilitates derivatization under mild conditions, while the electron-withdrawing fluorine enhances metabolic stability and modulates electronic properties in pharmaceutical intermediates.
(2-Amino-3-fluorophenyl)methanol serves as a versatile building block for the synthesis of fluorinated aromatic scaffolds, enabling efficient construction of heterocycles and bioactive intermediates. Its dual amine and alcohol functionalities provide orthogonal reactivity for selective derivatization, while the ortho-fluoro group facilitates subsequent nucleophilic substitution or transition-metal-catalyzed coupling reactions. The compound exhibits good bench stability and is readily purified by standard techniques, making it well-suited for iterative medicinal chemistry campaigns and process-scale applications.
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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 : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: