Название продукции:2,4-Dimethylthiazole-5-carbaldehyde
IUPAC Name:2,4-dimethyl-1,3-thiazole-5-carbaldehyde
| Упаковочная единица | Доступно для заказа | Цена ($) | Количество |
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| CM189979-5g | in stock | ƋƼɐ |
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| Product Overview |
2,4-Dimethylthiazole-5-carbaldehyde (DMTCA) is a versatile synthetic reagent that has been extensively studied and applied in various scientific fields. It is a five-membered heterocyclic compound with a thiazole ring and a carbaldehyde group. DMTCA is a colorless solid that is slightly soluble in water and has a melting point of about 110°C. It is widely used for the synthesis of different compounds, and its applications range from organic synthesis to medicinal chemistry. |
| Synthesis and Application |
2,4-Dimethylthiazole-5-carbaldehyde is synthesized by a two-step process involving the reaction of 2,4-diaminothiazole with carbon disulfide, followed by the oxidation of the resulting thiazole-2-carboxaldehyde with tert-butyl hydroperoxide. The reaction conditions are relatively mild and the yield of the product is high. 2,4-Dimethylthiazole-5-carbaldehyde has been widely used in various scientific research fields. It has been used as a reagent for the synthesis of different compounds, such as heterocyclic compounds, polymers, and dyes. It has also been used in the synthesis of pharmaceuticals and in the development of new materials. Additionally, 2,4-Dimethylthiazole-5-carbaldehyde has been used as a reagent in the synthesis of biologically active compounds, such as antibiotics and antifungal agents. |
| Future Directions |
The future directions for the use of 2,4-Dimethylthiazole-5-carbaldehyde in scientific research include the development of new synthetic methods, the synthesis of new compounds, and the investigation of its biochemical and physiological effects. Additionally, further research is needed to explore the potential applications of 2,4-Dimethylthiazole-5-carbaldehyde in the pharmaceutical and biomedical fields. Additionally, more research is needed to understand the mechanism of action of 2,4-Dimethylthiazole-5-carbaldehyde and to develop new methods for its synthesis. |
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