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191226-98-9 molecular structure
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tert-butyl N-[(2S,3R)-3-hydroxy-4-[N-(2-methylpropyl)4-nitrobenzenesulfonamido]-1-phenylbutan-2-yl]carbamate

ChemBase ID: 161569
Molecular Formular: C25H35N3O7S
Molecular Mass: 521.6263
Monoisotopic Mass: 521.21957148
SMILES and InChIs

SMILES:
c1c(ccc(c1)S(=O)(=O)N(C[C@H]([C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)O)CC(C)C)[N+](=O)[O-]
Canonical SMILES:
CC(CN(S(=O)(=O)c1ccc(cc1)[N+](=O)[O-])C[C@H]([C@H](Cc1ccccc1)NC(=O)OC(C)(C)C)O)C
InChI:
InChI=1S/C25H35N3O7S/c1-18(2)16-27(36(33,34)21-13-11-20(12-14-21)28(31)32)17-23(29)22(15-19-9-7-6-8-10-19)26-24(30)35-25(3,4)5/h6-14,18,22-23,29H,15-17H2,1-5H3,(H,26,30)/t22-,23+/m0/s1
InChIKey:
CQGKCZKCWMWXQP-XZOQPEGZSA-N

Cite this record

CBID:161569 http://www.chembase.cn/molecule-161569.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
tert-butyl N-[(2S,3R)-3-hydroxy-4-[N-(2-methylpropyl)4-nitrobenzenesulfonamido]-1-phenylbutan-2-yl]carbamate
IUPAC Traditional name
tert-butyl N-[(2S,3R)-3-hydroxy-4-[N-(2-methylpropyl)4-nitrobenzenesulfonamido]-1-phenylbutan-2-yl]carbamate
Synonyms
N-[(1S,2R)-2-Hydroxy-3-[(2-methylpropyl)[(4-nitrophenyl)sulfonyl]amino]-1-(phenylmethyl)propyl]-carbamic Acid 1,1-Dimethylethyl Ester
[(1S,2R)-1-Benzyl-2-hydroxy-3-[isobutyl[(4-nitro-phenyl)sulfonyl)]amino]propyl]-carbamic Acid tert-Butyl Ester
CAS Number
191226-98-9
PubChem SID
162255704
PubChem CID
10279676

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
TRC B279070 external link Add to cart
PubChem 10279676 external link
Data Source Data ID Price
TRC
B279070 external link Add to cart Please log in.
Data Source Data ID
PubChem 10279676 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 13.46877  H Acceptors
H Donor LogD (pH = 5.5) 4.348596 
LogD (pH = 7.4) 4.3485956  Log P 4.348596 
Molar Refractivity 136.9013 cm3 Polarizability 53.576202 Å3
Polar Surface Area 141.76 Å2 Rotatable Bonds 12 
Lipinski's Rule of Five false 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
Acetone expand Show data source
Chloroform expand Show data source
Dichloromethane expand Show data source
Ethyl Acetate expand Show data source
Apperance
White Solid expand Show data source
Storage Condition
Refrigerator expand Show data source
MSDS Link
Download expand Show data source
Certificate of Analysis
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DETAILS

DETAILS

TRC TRC
Toronto Research Chemicals - B279070 external link
A intermediate in the synthesis of Amprenavir, a selective HIV protease inhibitor.

REFERENCES

REFERENCES

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  • • 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)
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PATENTS

PATENTS

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INTERNET

INTERNET

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