2-Thiazolecarboxylic acid, 5-methyl-, ethyl ester


Chemical Name: 2-Thiazolecarboxylic acid, 5-methyl-, ethyl ester
CAS Number: 58334-08-0
Product Number: AG00EL9S(AGN-PC-03KBYQ)
Synonyms:
MDL No:
Molecular Formula: C7H9NO2S
Molecular Weight: 171.2169

Identification/Properties


Properties
BP:
248.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information


GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



Ethyl 5-methylthiazole-2-carboxylate is a versatile chemical compound widely used in chemical synthesis. This compound plays a crucial role in organic reactions due to its unique properties and functional groups. Specifically, it is commonly employed as a key building block in the preparation of various pharmaceuticals, agrochemicals, and flavor compounds.In chemical synthesis, Ethyl 5-methylthiazole-2-carboxylate serves as a valuable intermediate for the construction of complex molecules. Its thiazole ring structure imparts desirable characteristics to the final products, such as enhanced bioactivity or flavor profiles. By incorporating this compound into reaction schemes, chemists can access a diverse array of compounds with tailored properties.Furthermore, Ethyl 5-methylthiazole-2-carboxylate can participate in a variety of transformations, including esterification, alkylation, and ring-closure reactions. Its reactivity and compatibility with a range of functional groups make it a versatile tool for synthetic chemists seeking to create novel molecules with specific structures and functions.Overall, Ethyl 5-methylthiazole-2-carboxylate is a valuable component in the chemist's toolbox, enabling the efficient and strategic synthesis of a wide range of biologically active compounds, flavor additives, and specialty chemicals. Its versatility and utility make it an indispensable ingredient for the advancement of modern organic synthesis methodologies.