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Structure of 135807-51-1
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This boronate-bearing phenylacetic acid derivative features a protected amine group, enabling selective functionalization in complex synthetic sequences. The tert-butyl carbamate moiety ensures stability during handling and purification, while the carboxylic acid facilitates conjugation or derivatization under standard conditions.
2-(2-((tert-Butoxycarbonyl)amino)phenyl)acetic acid serves as a versatile building block for the synthesis of bioactive heterocycles and peptide conjugates. The protected amine enables orthogonal functionalization, while the pendant carboxylic acid facilitates coupling reactions under standard conditions. Its bench-stable tert-butyl carbamate group simplifies purification and allows selective deprotection in multistep sequences, making it well-suited for medicinal chemistry campaigns requiring precise structural control.
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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: