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Structure of 170097-87-7
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This tert-butoxycarbonyl-protected nicotinic acid derivative features a strategically positioned amino-methyl side chain, enabling straightforward incorporation into peptide synthesis workflows. The Boc group ensures stability during handling and provides orthogonal protection for amine functionalities in multistep conjugation processes.
6-(((tert-Butoxycarbonyl)amino)methyl)nicotinic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and peptide conjugates. The tert-butyl carbamate group provides stable protection of the primary amine under standard conditions, facilitating orthogonal functionalization. Its pyridine-carboxylic acid framework supports diverse transformations, including coupling reactions and cyclizations, while the bench-stable, crystalline nature simplifies handling and purification in multi-step syntheses.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: