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Structure of 4393-09-3
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2,3-Dimethoxybenzylamine features a benzylamine core adorned with methoxy groups at the 2- and 3-positions, enhancing solubility and electronic donation. This electron-rich scaffold enables efficient coupling in peptide synthesis and serves as a key building block for bioactive molecules. The compound exhibits bench-stable handling under standard conditions and integrates readily into diverse synthetic workflows.
2,3-Dimethoxybenzylamine serves as a versatile building block in medicinal chemistry and natural product synthesis, offering enhanced solubility and metabolic stability compared to unsubstituted analogs. The ortho-dimethoxy substitution pattern stabilizes the benzyl amine moiety against oxidation while enabling facile derivatization via reductive amination or coupling reactions. Its bench-stable, crystalline form facilitates handling and purification, making it ideal for constructing bioactive scaffolds and peptide conjugates in high-throughput screening campaigns.
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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: