2-((3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyclopentad1,3dioxol-4-yloxy)ethanol L-tataric acid
CAS 376608-65-0
CAS · 376608-65-0
Product Overview
2-((3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyclopentad1,3dioxol-4-yloxy)ethanol L-tataric acid is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.
Product Specifications
| Appearance | White or off-white powder or (and) particle |
|---|---|
| Identification (IR) | The infrared absorption spectrum of sample corresponds to that of reference substance |
| Identification (GC) | Under the Related substances item, the retention time of the main peak of the test solution should be consistent with that of the control solution |
| Related substances (152-7) | 0.10% max |
| Max unknown single impurity | 0.10% max |
| Total impurities | 1.0% max |
| Isomers (152-311Y) | 0.15% max |
| Water | 0.5% max |
| Loss on drying | 2.0% max |
| Residue on ignition | 0.5% max |
| Tartaric acid (as anhydrous substance) | 40.0% ~ 42.0% |
| Assay (On dried basis) | 98.0% ~ 102.0% |
Applications
2-((3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyclopentad1,3-dioxol-4-yloxy)ethanol L-tartaric acid is primarily used as a chiral building block and resolving agent in organic synthesis and pharmaceutical research. It is employed in the synthesis of enantiomerically pure compounds, including amino alcohol derivatives, pharmaceuticals, and fine chemicals. The compound's stereochemically defined structure makes it valuable for asymmetric synthesis, enabling the preparation of chiral intermediates for drug discovery and development. It is also applied in research for the production of ligands, catalysts, and functionalized molecules that require precise stereochemistry.
Benefits
The benefits of this compound include its well-defined chiral centers, which provide excellent stereochemical control in synthetic transformations. Its amino and hydroxyl functionalities allow for versatile derivatization and incorporation into complex molecules. The L-tartaric acid moiety enhances solubility and stability, facilitating handling and reproducibility in multi-step synthesis. By enabling efficient preparation of enantiomerically pure compounds, the compound supports high-yield, selective, and reliable synthesis of pharmaceuticals, catalysts, and bioactive molecules.
Conclusion
2-((3aR,4S,6R,6aS)-6-amino-2,2-dimethyltetrahydro-3aH-cyclopentad1,3-dioxol-4-yloxy)ethanol L-tartaric acid is a valuable chiral intermediate for asymmetric synthesis and enantiomerically pure compound preparation. Its stereochemical precision, functional versatility, and stability make it essential in pharmaceutical research, fine chemical synthesis, and catalyst development. By enabling controlled and efficient synthesis, it continues to play a critical role in advanced chemical and medicinal applications.
Previous
Next