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Structure of 34967-24-3
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3,5-Dimethoxybenzyl amine features a benzylamine scaffold adorned with two methoxy groups at the 3 and 5 positions, delivering enhanced solubility and stability. This electron-rich aryl moiety facilitates efficient coupling reactions in peptide synthesis and medicinal chemistry. The protected amine group enables straightforward derivatization, while the dimethoxy substitution improves metabolic resistance. Ideal for building bioactive scaffolds requiring hydrophilic character and robust handling under standard conditions.
3,5-Dimethoxybenzyl amine serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive scaffolds through amide coupling and reductive amination. Its electron-donating methoxy groups enhance solubility and metabolic stability, while the benzylic amine functionality offers high reactivity in standard coupling protocols. Bench-stable and readily purified by chromatography or crystallization, it functions efficiently in both small-molecule library synthesis and API intermediate development.
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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#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: