| Chemical Name: | 2lambda6-thia-5-azabicyclo[2.2.1]heptane-2,2-dione hydrochloride |
| CAS Number: | 1909336-43-1 |
| Product Number: | AG01C3A6(AG01C3A6) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C5H10ClNO2S |
| Molecular Weight: | 183.6564 |
2lambda6-thia-5-azabicyclo[2.2.1]heptane-2,2-dione hydrochloride, commonly referred to as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound exhibits unique reactivity and structural properties that make it highly valuable in various synthetic processes. In chemical synthesis, $name$ is utilized as a key intermediate for the preparation of complex organic molecules, enabling the construction of diverse molecular frameworks.$name$ is particularly favored in the synthesis of heterocyclic compounds, where its distinct bicyclic structure serves as a foundation for the introduction of different functional groups. Its cyclic nature and sulfur-containing ring provide a valuable scaffold for the creation of novel chemical entities with potential pharmaceutical or material applications. Additionally, the presence of the dione moiety in $name$ offers opportunities for further derivatization through selective functional group transformations.Moreover, the hydrochloride salt form of $name$ provides improved stability and solubility properties, facilitating its handling and utilization in various synthetic protocols. Through strategic incorporation into synthetic routes, 2lambda6-thia-5-azabicyclo[2.2.1]heptane-2,2-dione hydrochloride enables chemists to access a wide range of structurally diverse compounds, making it an indispensable tool in modern chemical synthesis.
![O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]](https://img.angenechemical.com/storage/3a59/3a5932eec850ab245f6f4d4a7f9497f9.png)
(Cl)Cl)c1c(C)cc(cc1C)C](https://img.angenechemical.com/storage/6693/66939a3f08a27d2b6717c3194e00970b.png)
