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Structure of 3342-78-7
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2-(2-Aminophenyl)acetic acid features a benzene ring bearing both amino and carboxylic acid functionalities in ortho proximity, enabling direct coordination to metal centers or integration into bioconjugation workflows. The pendant acetic acid group provides a handle for derivatization under standard coupling conditions, while the aromatic amine supports electrophilic substitution reactions. This scaffold exhibits enhanced solubility in polar solvents and maintains stability under ambient storage conditions.
2-(2-Aminophenyl)acetic acid serves as a versatile building block for synthesizing bioactive heterocycles and pharmaceutical intermediates. Its ortho-aminobenzoic acid scaffold enables efficient cyclization reactions, including intramolecular amide formation and electrophilic substitution. The molecule exhibits good bench stability, facilitates straightforward purification via crystallization or chromatography, and tolerates common functional groups under standard coupling conditions, making it well-suited for medicinal chemistry and process development workflows.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: