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Structure of 16310-13-7
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Thiazolidine-2-carboxylic acid features a stable heterocyclic scaffold with a carboxylic acid group at the 2-position, enabling direct integration into peptide synthesis. The thiazolidine ring imparts enhanced conformational rigidity and metabolic stability, making it valuable for bioactive molecule design. This compound serves as a key building block in medicinal chemistry and peptide-based drug discovery.
Thiazolidine-2-carboxylic acid serves as a versatile scaffold in medicinal chemistry, enabling the construction of heterocyclic motifs through well-established cyclization and functionalization pathways. Its inherent stability, combined with orthogonal reactivity of the thiazolidine ring and carboxylic acid group, facilitates straightforward derivatization for peptide mimetics and bioactive compound synthesis. Functions effectively in standard coupling and protection protocols, offering reliable performance in both solution-phase and solid-phase 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: