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Structure of 1108683-66-4
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(R)-4-(1-Aminoethyl)benzoic acid features a chiral α-amino group adjacent to a para-substituted aromatic ring, delivering a rigid, electron-rich scaffold for asymmetric synthesis. This bench-stable derivative integrates seamlessly into peptide-like architectures and serves as a key intermediate in the development of bioactive molecules requiring defined stereochemistry.
(R)-4-(1-Aminoethyl)benzoic acid serves as a chiral building block for bioactive molecules, enabling stereoselective synthesis of pharmaceutical intermediates. Its carboxylic acid and primary amine functionalities offer orthogonal reactivity for peptide coupling and conjugation strategies. The stable (R)-configuration facilitates reproducible asymmetric synthesis, while the benzoic acid core supports derivatization via standard electrophilic aromatic substitution and catalytic hydrogenation protocols.
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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: