methyl 5-chloro-1,3-thiazole-2-carboxylate


Chemical Name: methyl 5-chloro-1,3-thiazole-2-carboxylate
CAS Number: 98136-57-3
Product Number: AG0069L4(AGN-PC-0J0Y16)
Synonyms:
MDL No:
Molecular Formula: C5H4ClNO2S
Molecular Weight: 177.6088

Identification/Properties


Properties
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



Methyl 5-chlorothiazole-2-carboxylate is a versatile compound widely used in chemical synthesis as a key building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. This compound serves as an important intermediate in the synthesis of bioactive molecules due to its unique structural features and reactivity.One significant application of Methyl 5-chlorothiazole-2-carboxylate is its role in the synthesis of thiazole-based pharmaceuticals. Thiazole derivatives have shown promising biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. By incorporating Methyl 5-chlorothiazole-2-carboxylate into the molecular structure, chemists can modulate the pharmacological profile of the final compounds, enhancing their efficacy and selectivity.Furthermore, Methyl 5-chlorothiazole-2-carboxylate can be utilized in the preparation of agrochemicals such as pesticides and herbicides. Thiazole-containing compounds have demonstrated insecticidal and fungicidal activities, making them valuable tools in crop protection and pest management. The flexibility of Methyl 5-chlorothiazole-2-carboxylate in chemical transformations allows for the synthesis of diverse agricultural chemicals with tailored properties for specific applications.In addition to its pharmaceutical and agrochemical applications, Methyl 5-chlorothiazole-2-carboxylate can be employed in the synthesis of specialty chemicals and materials. Its ability to participate in various synthetic pathways enables the efficient construction of complex molecular structures with desired functionalities. Chemists can leverage the reactivity of Methyl 5-chlorothiazole-2-carboxylate to access novel compounds for research, industrial, and commercial purposes.