CAS 2161-68-4
:2-Thiazolamine, N,4-dimethyl-
Description:
2-Thiazolamine, N,4-dimethyl- is an organic compound characterized by its thiazole ring structure, which incorporates both sulfur and nitrogen atoms. This compound features a dimethyl substitution at the 4-position of the thiazole ring and an amino group at the 2-position, contributing to its basicity and potential reactivity. It is typically a white to off-white solid and is soluble in polar solvents, which is common for many thiazole derivatives. The presence of the amino group allows for hydrogen bonding, enhancing its solubility in water and other polar media. 2-Thiazolamine derivatives are of interest in various fields, including medicinal chemistry, due to their biological activity and potential applications in pharmaceuticals. The compound may exhibit properties such as antimicrobial or antifungal activity, making it a subject of research in drug development. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C5H8N2S
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Found 3 products.
N,4-Dimethylthiazol-2-amine
CAS:Formula:C5H8N2SPurity:95%Color and Shape:SolidMolecular weight:128.19544-Methyl-2-(methylamino)thiazole
CAS:4-Methyl-2-(methylamino)thiazolePurity:98%Molecular weight:128.20g/mol4-Methyl-2-(methylamino)thiazole
CAS:<p>4-Methyl-2-(methylamino)thiazole is an organic compound that is a bromination substrate, a palladium catalyst, and an inhibitor of cyclin-dependent kinases. It has been shown to be an effective inhibitor of the Suzuki coupling reaction. 4-Methyl-2-(methylamino)thiazole reacts with borane in the presence of a palladium catalyst to form 4-methylthiazoleboronic acid. This reaction can be used as a way to synthesize target products. 4-Methyl-2-(methylamino)thiazole also reacts with carbon monoxide and hydrogen cyanide to form 2,4-dimethoxybenzaldehyde in the presence of sodium hydroxide.</p>Formula:C5H8N2SPurity:Min. 95%Molecular weight:128.2 g/mol


