1000517-70-3 | 3-(2-Aminothiazol-5-yl)propan-1-ol

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Description

• Catalog Number: AA00701
• Chemical Name: 3-(2-Aminothiazol-5-yl)propan-1-ol
• CAS Number: 1000517-70-3
• Molecular Formula: C6H10N2OS
• Molecular Weight: 158.2214
• MDL Number: MFCD09927120
• SMILES: Nc1ncc(s1)CCCO

Upstream Synthesis Route

3-(2-Aminothiazol-5-yl)propan-1-ol, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure, containing both an aminothiazole and a propanol moiety, enables it to participate in a range of synthetic reactions, making it a valuable intermediate in organic chemistry.In chemical synthesis, $name$ can be used as a key starting material for the preparation of diverse compounds due to its functional groups and reactivity. For example, the amino group in the aminothiazole moiety can undergo numerous transformations such as acylation, alkylation, and amidation, allowing for the introduction of different substituents. The propanol group, on the other hand, can be modified through various functional group interconversions, expanding the molecule's synthetic utility.Moreover, 3-(2-Aminothiazol-5-yl)propan-1-ol exhibits chirality, making it an important precursor for the synthesis of enantiopure molecules. Its chiral center can be exploited in asymmetric synthesis to access optically pure compounds with enhanced biological activity or selectivity. Additionally, the thiazole ring present in the molecule provides a platform for constructing heterocyclic systems, which are prevalent in medicinal chemistry and material science.In summary, $name$ plays a crucial role in chemical synthesis by acting as a versatile building block that can be tailored to generate a diverse array of compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.