cas 944898-42-4|| where to buy 1-(2-Methylsulfanyl-3H-imidazol-4-yl)-ethanone

Название продукции:1-(2-Methylsulfanyl-3H-imidazol-4-yl)-ethanone

IUPAC Name:1-[2-(methylsulfanyl)-1H-imidazol-4-yl]ethan-1-one

: CAS：944898-42-4; Молекулярная формула：C6H8N2OS; Чистота：95%

: Номер в каталоге：CM187019; Молекулярная масса：156.2

Упаковочная единица	Доступно для заказа	Цена ($)	Количество
CM187019-1g	3-4 Weeks	ȤǠǺ

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Информация о продукции

: Номер CAS:944898-42-4; Молекулярная формула:C6H8N2OS; Точка плавления:-; Smiles-код:CC(C1=CNC(SC)=N1)=O; Плотность:

: Номер в каталоге:CM187019; Молекулярная масса:156.2; Точка кипения:; Номер Mdl:MFCD10696756; Хранение:

Category Infos

: Imidazoles; Imidazole is an important five-membered nitrogen-containing heterocyclic compound. Among the numerous heterocyclic compounds, imidazole and its derivatives are regarded as a unique and multifaceted scaffold material due to their diverse applications in industrial, organic and pharmaceutical chemistry. Imidazoles interact in different ways with many therapeutic targets, enzymes and receptors in biological systems and thus exhibit a wide range of biological activities. In particular, several imidazoles can be used as clinical drugs to treat various types of cancer with high therapeutic efficacy. Furthermore, imidazoles are one of the most critical segments in the field of anti-covid-19 virus drug discovery due to their ability to interact with active targets in living systems.; Imidazole Manufacturer; As a professional imidazole manufacturer, we can guarantee product quality and delivery time.our company has been committed to supply personalized product solutions to customers,pls consult us.

Product Other Information

Product Overview	1-(2-(Methylthio)-1H-imidazol-4-yl)ethanone, also known as MIE, it is a sulfur-containing heterocyclic compound.
Synthesis Method	1-(2-(Methylthio)-1H-imidazol-4-yl)ethanone is synthesized by reacting 2-methylthioimidazole with ethyl chloroacetate in the presence of a base. The reaction proceeds through nucleophilic substitution, and the resulting product is purified by column chromatography. The yield of this reaction is moderate, and the purity of the compound can be improved by recrystallization.
Chemical Properties	1-(2-(Methylthio)-1H-imidazol-4-yl)ethanone is also stable under normal laboratory conditions and can be stored for extended periods without degradation. It is readily available and can be synthesized in moderate yields.
Synthesis and Application	It has been shown to exhibit anti-inflammatory, anti-tumor, and anti-fungal activities. 1-(2-(Methylthio)-1H-imidazol-4-yl)ethanone has been tested against various cancer cell lines and has shown promising results in inhibiting cell proliferation and inducing apoptosis. Additionally, 1-(2-(Methylthio)-1H-imidazol-4-yl)ethanone has been found to have potent anti-inflammatory effects by suppressing the production of pro-inflammatory cytokines.
Future Directions	One area of interest is the development of 1-(2-(Methylthio)-1H-imidazol-4-yl)ethanone-based drugs for the treatment of cancer and inflammatory diseases. Further studies are needed to determine the optimal dosage and administration route for 1-(2-(Methylthio)-1H-imidazol-4-yl)ethanone. Additionally, more research is needed to understand the mechanism of action of 1-(2-(Methylthio)-1H-imidazol-4-yl)ethanone and its effects on various signaling pathways. Finally, studies on the toxicity and pharmacokinetics of 1-(2-(Methylthio)-1H-imidazol-4-yl)ethanone are needed to determine its safety and efficacy in humans.