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Structure of 771573-20-7
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This difluoromethoxyphenylamine derivative features a methoxy group at the 4-position and fluorine atoms at the 2,6-positions, enhancing electron-withdrawal and metabolic stability. The primary amine enables direct coupling in pharmaceutical synthesis, while the aryl framework supports integration into bioactive scaffolds requiring lipophilic character and targeted electronic tuning.
(2,6-Difluoro-4-methoxyphenyl)methanamine serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and pharmaceutical intermediates. Its electron-deficient aromatic core enhances metabolic stability, while the primary amine facilitates facile derivatization via amidation, alkylation, or reductive amination. Bench-stable and compatible with standard purification protocols, it functions effectively in coupling reactions and scaffold diversification for drug discovery campaigns.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 2735
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314-H318
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Precautionary Statements : P260-P264-P280-P304+P340-P330-P405-P501
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Lot numbers can be found on the outside label of a product: