| Chemical Name: | Ethanethioic acid, S-(1,1-dimethylethyl) ester |
| CAS Number: | 999-90-6 |
| Product Number: | AG003UFH(AGN-PC-0JMP34) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C6H12OS |
| Molecular Weight: | 132.22388 |
S-tert-Butyl thioacetate is a versatile compound commonly utilized in chemical synthesis due to its unique properties and reactivity. This specialized reagent serves as an essential building block in the creation of various organic molecules, particularly in the formation of sulfur-containing compounds.In chemical synthesis, S-tert-Butyl thioacetate acts as a sulfur source, facilitating the introduction of sulfur functional groups into target molecules with precision. Its distinctive tert-butyl group enhances the stability of the molecule, allowing for controlled reactions and efficient manipulations in synthetic pathways.Additionally, S-tert-Butyl thioacetate is commonly employed as a protecting group for thiol functionalities. By selectively blocking reactive thiol groups with this reagent, chemists can protect specific sites on complex molecules during multi-step syntheses. This protective function ensures the desired transformations occur only at predetermined positions, enabling the synthesis of intricate organic structures with high specificity.Furthermore, the use of S-tert-Butyl thioacetate in chemical synthesis enables chemists to access a wide range of sulfur-containing compounds that are valuable in medicinal chemistry, materials science, and other interdisciplinary fields. Its versatile applications make it a valuable tool for constructing diverse molecular architectures with tailored properties and functionalities, showcasing its significance in modern synthetic methodologies.
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