ethyl 3-(2-(((4-cyanophenyl)amino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate

ethyl 3-(2-(((4-cyanophenyl)amino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate

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

[(1S,3S)-3-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S,4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]carbamic acid tert-butyl ester

$250.00
CAS No.: 866030-35-5
Catalog No.: 110006
Purity: 95%
MF: C30H49NO7
MW: 535.722
Storage: 2-8 degree Celsius
SMILES: COCCCOC1=CC(C[C@@H](C[C@H](NC(=O)OC(C)(C)C)[C@@H]2C[C@@H](C(C)C)C(=O)O2)C(C)C)=CC=C1OC
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[(1S,3S)-3-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S,4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]carbamic acid tert-butyl ester; CAS No.: 866030-35-5; As a custom chemical synthesis company, we deliver complex pentyl carbamates for HCV NS5A inhibitor development. The (1S,3S)-configured diarylmethyl group and tetrahydrofuranyl moiety enable viral replication complex disruption. Our synthetic route combines enzymatic desymmetrization with Ullmann coupling for efficient assembly. The tert-butyloxycarbonyl (Boc) protection allows sequential deblocking in multi-step antiviral drug synthesis.

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