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Structure of 840501-15-7
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(4-Amino-2-fluorophenyl)methanol features a strategically positioned amino group and fluorine atom on the aromatic ring, enabling enhanced electronic modulation and metabolic stability. This bench-stable phenolic alcohol integrates readily into bioactive scaffolds, offering high compatibility in coupling reactions and serving as a key intermediate for pharmaceutical and agrochemical development.
(4-Amino-2-fluorophenyl)methanol serves as a versatile building block for the synthesis of fluorinated aromatic amines and heterocyclic scaffolds. Its dual functionality—primary amine and benzylic alcohol—enables selective transformations, including coupling reactions, derivatization, and cyclization processes. The molecule exhibits good bench stability and compatibility with standard purification techniques, facilitating integration into medicinal chemistry and process development workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: