5-Ethyl-4-methylthiazole is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. This compound features an ethyl group and a methyl group attached to the thiazole ring, contributing to its unique chemical properties. It is typically a colorless to pale yellow liquid with a distinctive odor, often described as having a savory or meaty scent, which makes it of interest in the flavor and fragrance industry. The molecular formula of 5-Ethyl-4-methylthiazole reflects its composition, and it is known for its stability under standard conditions. It is soluble in organic solvents and has limited solubility in water. The compound is utilized in various applications, including as a flavoring agent in food products and as a potential building block in organic synthesis. Safety data indicates that, like many thiazole derivatives, it should be handled with care, as it may pose health risks if ingested or inhaled in significant quantities.

5-Ethyl-4-methylthiazole

31883-01-9: 4-Methyl-5-ethylthiazole, 5-Ethyl-4-Methyl-1,3-Thiazole, Thiazole, 5-ethyl-4-methyl-, 5-Ethyl-4-methylthiazole

5-ethyl-4-methylthiazole

5-Ethyl-4-methylthiazole is a versatile compound that exhibits substrate specificity in various biochemical reactions. It is commonly used as a buffered acetal in the industrial production of fragrances, particularly in the synthesis of Coelogyne flaccida fragrance. Additionally, this compound has been found to have antioxidative properties, protecting against oxidative damage caused by free radicals. In the field of organic synthesis, 5-Ethyl-4-methylthiazole serves as a precursor for the synthesis of various amines and glycine derivatives. It has also been identified as a metabolite in mice and is used as a research chemical for scientific studies. Furthermore, this compound finds applications in the development of herbicides and nitrating agents. Its solubility in dimethyl sulfoxide makes it suitable for use in different experimental setups.

CAS 31883-01-9: 5-Ethyl-4-methylthiazole

5-Ethyl-4-methylthiazole

Ref: 10-F223007

5-ethyl-4-methylthiazole

Ref: IN-DA00BZSO

5-Ethyl-4-methylthiazole

Ref: 3D-GBA88301