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Structure of 437-83-2
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3-Fluoro-2-methoxyaniline features a fluorinated aromatic ring paired with a methoxy group, delivering enhanced electron density and metabolic stability. This ortho-substituted aniline integrates readily into pharmaceutical intermediates, enabling efficient coupling reactions under standard conditions. The compound exhibits robust bench stability and facilitates the synthesis of bioactive molecules requiring precise electronic tuning.
3-Fluoro-2-methoxyaniline serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocycles and pharmaceutical intermediates. Its ortho-substituted aryl amine functionality offers enhanced reactivity in electrophilic aromatic substitution and coupling reactions, while the methoxy and fluoro groups provide favorable electronic modulation and metabolic stability. The compound exhibits good bench stability and is compatible with standard synthetic workflows, facilitating efficient purification and integration into multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301+H311-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: