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[(1S,2R)-1-Benzyl-2-hydroxy-3-[isobutyl-d9-[(4-nitrophenyl)sulfonyl]amino]propyl]carbamic Acid tert-Butyl Ester_Molecular_structure_CAS_)
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[(1S,2R)-1-Benzyl-2-hydroxy-3-[isobutyl-d9-[(4-nitrophenyl)sulfonyl]amino]propyl]carbamic Acid tert-Butyl Ester

Catalog No. B279072 Name Toronto Research Chemicals
CAS Number Website http://www.trc-canada.com
M. F. C25H35N3O7S Telephone +1 (416) 665-9696
M. W. 521.6263 Fax +1 (416) 665-4439
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Storage Chembase ID: 161570

SYNONYMS

IUPAC name
tert-butyl N-[(2S,3R)-3-hydroxy-4-{N-[2-(2H3)methyl(2H6)propyl]4-nitrobenzenesulfonamido}-1-phenylbutan-2-yl]carbamate
IUPAC Traditional name
tert-butyl N-[(2S,3R)-3-hydroxy-4-{N-[2-(2H3)methyl(2H6)propyl]4-nitrobenzenesulfonamido}-1-phenylbutan-2-yl]carbamate
Synonyms
N-[(1S,2R)-2-Hydroxy-3-[(2-methylpropyl-d9)[(4-nitrophenyl)sulfonyl]amino]-1-(phenylmethyl)propyl]carbamic Acid 1,1-Dimethylethyl Ester

DATABASE IDS

PROPERTIES

Certificate of Analysis Download
Apperance Off-White Solid
Solubility Chloroform
Solubility Dichloromethane
Solubility Ethyl Acetate
MSDS Link Download

DETAILS

Description (English)
An intermediate in the synthesis of labelled Amprenavir, a selective HIV protease inhibitor.

REFERENCES

  • Dorsey, B., et al.: J. Med. Chem., 37, 3443 (1994)
  • Gong, Y., et al.: Antimicrob. Agents Chemother., 44, 2319 (1994)
  • Maeda, K., et al.: J. Biol. Chem., 276, 35194 (1994)