![(1S,2R,3S,5R)-3-(phenylmethoxy)-2-[(phenylmethoxy)methyl]-6-oxabicyclo[3.1.0]hexane](https://www.chemshuttle.com/media/catalog/product/cache/31dbf0bffbfa69a5826a72cec9a446de/1/0/109915_2.jpg)
2-(((3ar,4s,6r,6as)-6-aminotetrahydro-2,2-dimethyl-4h-cyclopenta-1,3-dioxol-4-yl)oxy)ethanol ethanedioate
$300.00
CAS No.: 1215268-15-7
Catalog No.: 109927
Purity: 95%
MF: C12H21NO8
MW: 307.299
Storage: 2-8 degree Celsius
SMILES: OC(=O)C(O)=O.[H][C@@]12OC(C)(C)O[C@]1([H])[C@H](C[C@H]2N)OCCO
Catalog No.: 109927
Purity: 95%
MF: C12H21NO8
MW: 307.299
Storage: 2-8 degree Celsius
SMILES: OC(=O)C(O)=O.[H][C@@]12OC(C)(C)O[C@]1([H])[C@H](C[C@H]2N)OCCO
2-(((3ar,4s,6r,6as)-6-aminotetrahydro-2,2-dimethyl-4h-cyclopenta-1,3-dioxol-4-yl)oxy)ethanol ethanedioate; CAS No.: 1215268-15-7; ChemShuttle provides cycle compounds like this aminocyclopentanediol oxalate salt, a carbocyclic nucleoside precursor. The (3aR,4S,6R,6aS)-configuration ensures proper sugar mimicry for viral polymerase inhibition. Our synthetic methodology features RCM (ring-closing metathesis) for cyclopentene formation and diastereoselective dihydroxylation. The oxalate counterion optimizes crystallinity for X-ray structural analysis in antiviral mechanism studies.
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