2-{[(3aR,4S,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol (2R,3R)-2,3-dihydroxysuccinate CAS: 376608-65-0
Catalog Number | XD93935 |
Product Name | 2-{[(3aR,4S,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol (2R,3R)-2,3-dihydroxysuccinate |
CAS | 376608-65-0 |
Molecular Formula | C14H25NO10 |
Molecular Weight | 367.35 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
2-{[(3aR,4S,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol (2R,3R)-2,3-dihydroxysuccinate is a compound with a complex chemical structure consisting of a cyclopenta[d][1,3]dioxol ring, an amino group, and an ethanol moiety, among others. This compound has various potential applications in the field of pharmaceuticals and chemical synthesis due to its unique properties.One potential use of 2-{[(3aR,4S,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol (2R,3R)-2,3-dihydroxysuccinate is as a pharmaceutical intermediate. It can serve as a building block for the synthesis of complex molecules with potential therapeutic benefits. The cyclopenta[d][1,3]dioxol ring in the structure acts as a core scaffold for the attachment of various functional groups, allowing for the creation of diverse compounds.The presence of the amino group in the structure of this compound makes it particularly interesting for medicinal chemistry. It can potentially be modified or derivatized to introduce specific properties or enhance the bioactivity of drug candidates. The compounds derived from 2-{[(3aR,4S,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol (2R,3R)-2,3-dihydroxysuccinate may exhibit enhanced pharmacological properties, such as increased efficacy or reduced toxicity, compared to their parent compounds.Furthermore, the presence of the 2,3-dihydroxy succinate moiety offers potential applications in the field of chemical synthesis. This compound can act as a chiral building block, providing a source of chirality in the synthesis of other molecules. Chirality, or the existence of mirror-image isomers, plays a fundamental role in many biological processes and pharmaceutical interactions. The chiral properties of the 2,3-dihydroxy succinate group allow for the creation of enantiomerically pure compounds, which can have significant implications in drug development and manufacturing.It is worth noting that the specific applications of 2-{[(3aR,4S,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol (2R,3R)-2,3-dihydroxysuccinate may vary, depending on the desired properties and requirements of the final product. Additionally, further research and development are necessary to explore the full potential of this compound in various fields.As with any chemical compound, proper handling, storage, and safety protocols should be followed when working with 2-{[(3aR,4S,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol (2R,3R)-2,3-dihydroxysuccinate to ensure personal safety and prevent any environmental hazards.In conclusion, 2-{[(3aR,4S,6R,6aS)-6-Amino-2,2-dimethyltetrahydro-3aH-cyclopenta[d][1,3]dioxol-4-yl]oxy}ethanol (2R,3R)-2,3-dihydroxysuccinate has potential applications as a pharmaceutical intermediate and chiral building block. Its structural features, including the cyclopenta[d][1,3]dioxol ring, amino group, and 2,3-dihydroxy succinate moiety, offer opportunities for the creation of diverse compounds with enhanced bioactivity and chirality. Further research and development are required to explore its full potential in various fields.