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Structure of 221285-25-2
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This boronate moiety integrates a fluorinated aromatic scaffold with a reactive hydroxymethyl group, enabling efficient coupling in transition-metal-catalyzed transformations. The para-fluorine substituent enhances electrophilicity while maintaining stability under standard conditions.
(2-Amino-6-fluorophenyl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted anilines and heterocyclic scaffolds. Its dual amino and hydroxymethyl functionalities offer orthogonal reactivity for coupling, derivatization, and protection strategies. The molecule exhibits good bench stability and compatibility with standard purification methods, facilitating integration into multi-step synthetic sequences for 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: