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(2S,3S,5S)-2-(N,N-Dibenzylamino)-3-hydroxy-5-(tert-butyloxycarbonylamino)-1,6-diphenylhexane_Molecular_structure_CAS_162849-93-6)
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(2S,3S,5S)-2-(N,N-Dibenzylamino)-3-hydroxy-5-(tert-butyloxycarbonylamino)-1,6-diphenylhexane

Catalog No. D416954 Name Toronto Research Chemicals
CAS Number 162849-93-6 Website http://www.trc-canada.com
M. F. C37H44N2O3 Telephone +1 (416) 665-9696
M. W. 564.75686 Fax +1 (416) 665-4439
Purity Email info@trc-canada.com
Storage -20°C Freezer Chembase ID: 166863

SYNONYMS

IUPAC name
tert-butyl N-[(2S,4S,5S)-5-(dibenzylamino)-4-hydroxy-1,6-diphenylhexan-2-yl]carbamate
IUPAC Traditional name
tert-butyl N-[(2S,4S,5S)-5-(dibenzylamino)-4-hydroxy-1,6-diphenylhexan-2-yl]carbamate
Synonyms
[(1S,3S,4S)-4-[Bis(phenylmethyl)amino]-3-hydroxy-5-phenyl-1-(phenylmethyl)pentyl]carbamic Acid 1,1-Dimethylethyl Ester

DATABASE IDS

CAS Number 162849-93-6

PROPERTIES

Certificate of Analysis Download
Apperance Pale Yellow Solid
Melting Point 40-42°C
Solubility Chloroform
Solubility Dichloromethane
Solubility Methanol
MSDS Link Download
Storage Condition -20°C Freezer

DETAILS

Description (English)
(2S,3S,5S)-2-(N,N-Dibenzylamino)-3-hydroxy-5-(tert-butyloxycarbonylamino)-1,6-diphenylhexane is an intermediate in the synthesis of Lopinavir(L469480) and Ritonavir (R535000).

REFERENCES

  • Stoner, E., et al.: Org. Process Res. Develop., 4, 264 (2000)