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Structure of 147969-86-6
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This piperidine-based benzoic acid derivative integrates a tert-butyl carbamate-protected amine and a methylene-linked aromatic carboxylic acid, enabling seamless incorporation into peptide conjugation workflows. The protected amine facilitates selective derivatization under standard conditions, while the carboxylic acid group serves as a robust anchor point for coupling reactions in synthetic medicinal chemistry.
4-((1-(tert-Butoxycarbonyl)piperidin-4-yl)methyl)benzoic acid serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. The molecule combines a robust tert-butyl carbamate-protected piperidine with a benzoic acid handle, enabling facile functionalization via standard coupling reactions. Its bench-stable Boc group permits orthogonal deprotection, while the aromatic carboxylic acid facilitates conjugation in peptide-like systems and macrocyclization strategies.
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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: