4-nitrobenzyl (2S,4S)-4-acetylthio-2-[[N-sulfamoyl-N-(tert-butoxycarbonyl)amino]methyl]pyrrolidine-1-carboxylate

4-nitrobenzyl (2S,4S)-4-acetylthio-2-[[N-sulfamoyl-N-(tert-butoxycarbonyl)amino]methyl]pyrrolidine-1-carboxylate

2a,3a-Epoxy-16b-(1-pyrrolidinyl)-5a-androstan-17b-ol

2a,3a-Epoxy-16b-(1-pyrrolidinyl)-5a-androstan-17b-ol

(2R,5S)-5-(4-amino-5-fluoro-2-oxo-1(2H)-pyrimidinyl)-1,3-oxathiolane-2-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester

$300.00
CAS No.: 764659-72-5
Catalog No.: 109997
Purity: 95%
MF: C18H26FN3O4S
MW: 399.488
Storage: 2-8 degree Celsius
SMILES: CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(=O)[C@@H]1O[C@@H](CS1)N1C=C(F)C(N)=NC1=O
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(2R,5S)-5-(4-amino-5-fluoro-2-oxo-1(2H)-pyrimidinyl)-1,3-oxathiolane-2-carboxylic acid (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexyl ester; CAS No.: 764659-72-5; This oxathiolane carboxylate exemplifies ChemShuttle s heterocycles expertise for antiviral nucleoside analogs. The (2R,5S) configuration mimics natural ribose stereochemistry. Our enzymatic desymmetrization achieves >99% ee in oxathiolane formation. The menthyl ester enhances crystallinity for purification, supporting development of hepatitis B virus reverse transcriptase inhibitors.

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