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Structure of 1699713-02-4
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This protected amino acid derivative features a tert-butoxycarbonyl-methylamino side chain appended to a benzoic acid core. The Boc group provides orthogonal protection for amine functionalities, enabling selective deprotection during peptide synthesis. The molecule exhibits enhanced solubility and stability under standard bench conditions, facilitating handling in multi-step organic transformations.
2-(((Tert-butoxycarbonyl)(methyl)amino)methyl)benzoic acid serves as a versatile building block for peptide and heterocyclic synthesis, offering orthogonal protection of both amine and carboxylic acid functionalities. The Boc-methylamino side chain enables selective deprotection under mild acidic conditions, while the benzoic acid moiety facilitates coupling reactions with amines or alcohols. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step synthetic sequences in medicinal chemistry and API development.
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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: