CAS 299417-31-5
:2-Thiazolamine,5-(1,1-dimethylethyl)-
Description:
2-Thiazolamine,5-(1,1-dimethylethyl)- is an organic compound characterized by the presence of a thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. This compound features an amine functional group, indicating its potential basicity and ability to participate in various chemical reactions, such as nucleophilic substitutions. The presence of the tert-butyl group (1,1-dimethylethyl) enhances its hydrophobic characteristics, which can influence its solubility and reactivity in different solvents. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Additionally, its structural features suggest potential applications in agrochemicals or as a building block in organic synthesis. As with many thiazole derivatives, it may also display interesting properties such as antimicrobial or antifungal activity, although specific biological effects would require further investigation. Overall, 2-Thiazolamine,5-(1,1-dimethylethyl)- is a versatile compound with potential applications across various fields of chemistry and pharmacology.
Formula:C7H12N2S
Synonyms:- (5-tert-Butylthiazol-2-yl)amine
- 2-Amino-5-tert-butylthiazole
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Found 4 products.
2-Thiazolamine, 5-(1,1-dimethylethyl)-
CAS:Formula:C7H12N2SPurity:96%Color and Shape:SolidMolecular weight:156.24865-(tert-Butyl)thiazol-2-amine
CAS:5-(tert-Butyl)thiazol-2-aminePurity:96%Molecular weight:156.25g/mol5-tert-butyl-1,3-thiazol-2-amine
CAS:Formula:C7H12N2SPurity:96%Color and Shape:SolidMolecular weight:156.255-tert-Butyl-1,3-thiazol-2-amine
CAS:<p>5-tert-Butyl-1,3-thiazol-2-amine is an aromatic compound with the molecular formula CHN. This compound is a colorless solid that is soluble in water and alcohol. It can be used as a substitute for 2-aminothiazole, which belongs to the group of halogenated compounds. 5-tert-Butyl-1,3-thiazol-2-amine has been shown to react with alkyl halides to form alkylated products. The reaction with alkyl halides may be due to its primary amino group and amino group. 5-tert-Butyl-1,3-thiazol-2-amine also reacts with sulfuric acid and sulfuric acid salts to form thiazoles and thiazolones.</p>Formula:C7H12N2SPurity:Min. 95%Molecular weight:156.25 g/mol




