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Structure of 669713-92-2
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Boc-amino-3-chlorophenylacetic acid serves as a key building block in peptide synthesis and medicinal chemistry. The tert-butoxycarbonyl group provides stable protection of the amine, while the 3-chlorophenylacetic moiety offers a hydrophobic, electron-deficient aromatic handle for downstream functionalization. This compound enables efficient coupling under standard conditions.
Boc-3-chlorophenylglycine serves as a versatile building block for peptide synthesis and medicinal chemistry, enabling efficient incorporation of a 3-chlorophenylalanine derivative. The tert-butoxycarbonyl (Boc) group provides robust protection of the amine, ensuring stability during storage and compatibility with standard deprotection protocols. Its ortho-chloro-substituted aromatic ring offers favorable electronic and steric properties for downstream functionalization. The molecule exhibits excellent bench stability, ease of purification, and broad functional group tolerance in coupling reactions, facilitating its use in constructing bioactive scaffolds and heterocyclic systems.
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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: