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Structure of 142121-95-7
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This protected amino acid derivative features a tert-butoxycarbonyl group for stable peptide coupling and a 3,4-dichlorophenyl moiety that enhances lipophilicity and metabolic stability. The carboxylic acid functionality enables direct conjugation or further derivatization under standard conditions.
2-((tert-Butoxycarbonyl)amino)-2-(3,4-dichlorophenyl)acetic acid serves as a versatile building block for the synthesis of bioactive heterocycles and peptide derivatives. Its tert-butyl carbamate group enables orthogonal protection of amines, while the α-amino acid scaffold facilitates coupling reactions with minimal racemization. The molecule exhibits excellent bench stability, ease of purification, and compatibility with standard deprotection protocols, making it ideal for medicinal chemistry campaigns targeting CNS and metabolic disease targets.
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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: