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Ethyl 2-aminothiazole-5-carboxylate CAS: 32955-21-8

Short Description:

Catalog Number: XD93773
Cas: 32955-21-8
Molecular Formula: C6H8N2O2S
Molecular Weight: 172.2
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Product Tags

Catalog Number XD93773
Product Name Ethyl 2-aminothiazole-5-carboxylate
CAS 32955-21-8
Molecular Formula C6H8N2O2S
Molecular Weight 172.2
Storage Details Ambient

Product Specification

Appearance White powder
Assay 99% min

 

Ethyl 2-aminothiazole-5-carboxylate is a chemical compound with a unique structure that holds significant potential for various applications in scientific research and industrial processes. This compound, also known as ethyl 2-amino-4-thiazolecarboxylate, consists of an ethyl ester group attached to a 2-aminothiazole ring with a carboxylate group.One important application of ethyl 2-aminothiazole-5-carboxylate is in medicinal chemistry. Thiazole derivatives are well-known for their diverse biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. This compound can serve as a starting point for the development of potential therapeutics or chemical probes targeting specific diseases or biological processes. Researchers can modify its chemical structure to optimize its drug-like properties, such as solubility, metabolic stability, and target selectivity.Additionally, ethyl 2-aminothiazole-5-carboxylate can be utilized in the synthesis of heterocyclic compounds. The presence of the thiazole ring and the carboxylate group offers opportunities for it to undergo various chemical transformations, such as condensations, substitutions, or cyclizations. Organic chemists can employ this compound as a building block to construct more complex molecules with diverse applications, including pharmaceuticals, agricultural chemicals, or materials science.In material science, this compound can find utility in the design and synthesis of functional materials. Its unique structure and distinctive properties make it a potential candidate for materials with applications in optoelectronics, sensors, or catalysts. The thiazole ring and the carboxylate group can provide conjugation and coordination sites, respectively, allowing for the incorporation of this compound into polymer matrices or as a component in composite materials.As with any chemical compound, proper safety protocols should be followed when handling ethyl 2-aminothiazole-5-carboxylate. Safety data sheets and guidelines from regulatory agencies should be consulted to ensure safe laboratory practices and disposal methods.In summary, ethyl 2-aminothiazole-5-carboxylate holds promise for various applications in medicinal chemistry, organic synthesis, and material science. Its unique structure and potential biological activities make it a valuable tool for drug discovery and development. Additionally, its versatility in organic synthesis allows for the construction of complex molecules for different purposes. Finally, its potential in material science opens up possibilities for the development of functional materials with unique properties. Safety should always be a priority when working with this compound.


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    Ethyl 2-aminothiazole-5-carboxylate CAS: 32955-21-8