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| Chemical manufacturer since 2012 | ||||
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| Classification | Chemical reagent >> Organic reagent >> Ester >> Ethyl ester compound |
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| Name | Ethyl 2-(3-formyl-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylate |
| Molecular Structure | ![]() |
| Molecular Formula | C18H21NO4S |
| Molecular Weight | 347.43 |
| CAS Registry Number | 161798-03-4 |
| EC Number | 700-743-7 |
| SMILES | CCOC(=O)C1=C(N=C(S1)C2=CC(=C(C=C2)OCC(C)C)C=O)C |
| Density | 1.183 |
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| Hazard Statements | H315-H319 Details | ||||||||||||||||
| Precautionary Statements | P264-P264+P265-P280-P302+P352-P305+P351+P338-P321-P332+P317-P337+P317-P362+P364 Details | ||||||||||||||||
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| SDS | Available | ||||||||||||||||
| Ethyl 2-(3-formyl-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylate, commonly referred to as formyl-isobutoxyphenyl thiazole carboxylate, emerged from ongoing chemical research into thiazole derivatives. The compound was synthesized through efforts to functionalize thiazole rings with aldehyde and isobutoxyphenyl groups, leveraging the unique chemical reactivity of these moieties. Researchers combined 3-formyl-4-isobutoxybenzaldehyde with thioamide and ethyl chloroacetate in a multi-step reaction to obtain this novel compound. Its synthesis highlighted the potential of thiazole derivatives for creating new molecules with diverse biological and chemical properties, opening pathways for innovative applications in various fields including pharmaceuticals, materials science, and agrochemicals. |
| Market Analysis Reports |
| List of Reports Available for Ethyl 2-(3-formyl-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylate |