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Structure of 232275-73-9
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This protected amino acid derivative features a tert-butoxycarbonyl group that stabilizes the amine functionality, enabling reliable incorporation into peptide synthesis workflows. The para-chloro substituent enhances electrophilic reactivity and provides a handle for downstream functionalization. Designed for robust handling under standard bench conditions, this compound integrates seamlessly into multi-step organic transformations requiring controlled nitrogen protection and strategic halogen placement.
4-((tert-Butoxycarbonyl)amino)-2-chlorobenzoic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted benzimidazoles and other heterocyclic scaffolds. The protected amine and carboxylic acid functionalities offer orthogonal reactivity, facilitating sequential transformations in multi-step syntheses. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for peptide-like and small-molecule library development.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: