ethyl 2-((dimethylamino)methyl)thiazole-4-carboxylate

ethyl 2-((dimethylamino)methyl)thiazole-4-carboxylate

methyl 2-(chloromethyl)thiazole-4-carboxylate

methyl 2-(chloromethyl)thiazole-4-carboxylate

ethyl 2-(3,5-dichlorophenyl)thiazole-4-carboxylate

$300.00
CAS No.: 132089-38-4
Catalog No.: 196070
Purity: 95%
MF: C12H9Cl2NO2S
MW: 302.182
Storage: 2-8 degree Celsius
SMILES: ClC=1C=C(C=C(C1)Cl)C=1SC=C(N1)C(=O)OCC
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ethyl 2-(3,5-dichlorophenyl)thiazole-4-carboxylate; CAS No.: 132089-38-4; ethyl 2-(3,5-dichlorophenyl)thiazole-4-carboxylate. PROPERTIES: Ethyl 2-(3,5-dichlorophenyl)thiazole-4-carboxylate is a crystalline solid with a molecular weight of approximately 302.1 g/mol. It has a melting point between 105-110 C. The compound is moderately soluble in common organic solvents like dichloromethane and acetone but is practically insoluble in water. It exhibits characteristic absorption in the UV spectrum around 260 nm due to the conjugated system between the thiazole ring and the dichlorophenyl group. For proper storage, keep in a tightly sealed container at room temperature away from heat sources. Safety: This compound may cause long-term adverse effects in the aquatic environment. It is advisable to avoid release to the environment and use closed systems for handling. In case of fire, use water spray, foam, dry chemical, or carbon dioxide. APPLICATIONS: In pharmaceutical research, ethyl 2-(3,5-dichlorophenyl)thiazole-4-carboxylate is used as a lead compound for developing anticancer agents. The dichlorophenyl group provides lipophilicity that enhances cellular uptake. In agrochemical applications, derivatives of this compound are explored for fungicidal properties. The thiazole ring system provides structural features that inhibit fungal enzyme activity. In materials science, it is used as a building block for creating liquid crystalline materials. The combination of the thiazole ring and the dichlorophenyl group creates anisotropic molecules suitable for liquid crystal applications. These applications are documented in medicinal chemistry journals and materials science research articles.

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