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2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylicacid CAS:302964-02-9

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Catalog Number: XD95798
Cas: 302964-02-9
Molecular Formula: C9H12N2O4S
Molecular Weight: 244.27
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Product Detail

Product Tags

Catalog Number XD95798
Product Name 2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylicacid
CAS 302964-02-9
Molecular Formula C9H12N2O4S
Molecular Weight 244.27
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylic acid, also known as Boc-thiazole-5-carboxylic acid, is a compound that possesses unique properties and potential effects in various fields, including medicinal chemistry and organic synthesis.One of the notable effects of Boc-thiazole-5-carboxylic acid is its ability to serve as a key building block for the synthesis of diverse molecules. Its thiazole ring structure provides opportunities for functional group modification and derivatization, allowing for the creation of novel compounds with enhanced properties. This versatility makes Boc-thiazole-5-carboxylic acid a valuable tool in drug discovery and development, as it enables the synthesis of potential therapeutic agents with targeted mechanisms of action.Moreover, Boc-thiazole-5-carboxylic acid possesses acidic properties due to the presence of a carboxylic acid group. This acidity can be exploited in chemical transformations, such as esterification and amidation reactions, where the carboxylic acid functionality plays a crucial role in the formation of new bonds. These reactions allow for the introduction of various substituents onto the thiazole ring, leading to the development of structurally diverse compounds with unique biological activities.Additionally, Boc-thiazole-5-carboxylic acid is capable of forming stable amide bonds. This property is particularly relevant in peptide synthesis, where it can be employed as a protected amino acid in the construction of peptide chains. The tert-butoxycarbonyl (Boc) group acts as a protecting group for the amine functionality, ensuring its stability during the synthesis process while allowing for selective reactions with other functional groups. This protection strategy enables the stepwise assembly of complex peptides with high purity and yield.Furthermore, Boc-thiazole-5-carboxylic acid has demonstrated potential in the field of material science. Its unique structure and reactivity enable the incorporation of thiazole moieties into polymers, leading to the development of materials with desired properties such as conductivity and thermal stability. These materials find applications in various technological fields, including electronics, energy storage, and sensors.In summary, Boc-thiazole-5-carboxylic acid exhibits diverse effects and plays a significant role in organic synthesis, medicinal chemistry, and material science. Its versatile nature and ability to form stable bonds make it a valuable building block in the synthesis of complex molecules and peptides. Moreover, its unique structural properties open up opportunities for the development of novel therapeutic agents and functional materials. Overall, Boc-thiazole-5-carboxylic acid holds promise as a versatile tool in scientific research and development.


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    2-[(tert-butoxycarbonyl)amino]-1,3-thiazole-5-carboxylicacid CAS:302964-02-9