(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane

(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane
  • CAS No.:98737-29-2
Other grades of this product :
(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane Basic information
Product Name:(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane
Synonyms:tert-Butyl [(S)-1-[(S)-Oxiran-2-yl]-2-phenylethyl]carbamate (2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane;(2R,3S)-1,2-Epoxy-3-(Boc-aMino)-4-phenylbutane, 95+%;(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane 99%;(2S,3S)-3-Boc-amino-1,2-epoxy-4-phenylbutane, >=99%;3S-(T-BOC)AMINO-1,2-(S)-EPOXY-4-PHENYLBUTANE;[(1S)-1-((2S)-Oxiranyl)-2-phenylethyl]carbaMic Acid tert-Butyl;TERT-BUTYL [S-(R,R)]-(-)-(1-OXIRANYL-2-PHENYLETHYL)CARBAMATE;T-BUTYL [S-(R*,R*)]-(-)-(1-OXIRANYL-2-PHENYLETHYL)CARBAMATE
CAS:98737-29-2
MF:C15H21NO3
MW:263.33
EINECS:425-420-5
Product Categories:API intermediates;Aromatics Compounds;chiral;Aromatics;Chiral Reagents;Heterocycles
Mol File:98737-29-2.mol
(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane Chemical Properties
Melting point 125-127 °C(lit.)
alpha -7°(23℃, c=0.6, CH3OH)
Boiling point 398.8±25.0 °C(Predicted)
density 1.118±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
form powder to crystal
pka12.19±0.46(Predicted)
color White to Almost white
optical activity[α]23/D 7°, c = 0.6 in methanol
Water Solubility Insoluble in water. Soluble in Chloroform, Dichloromethane and Ethyl Acetate.
InChIKeyNVPOUMXZERMIJK-QWHCGFSZSA-N
CAS DataBase Reference98737-29-2(CAS DataBase Reference)
Safety Information
Hazard Codes F,Xi,N
Risk Statements 10-36/37/38-50/53
Safety Statements 7/9-16-26-36/37/39-61-60
RIDADR UN 3077 9 / PGIII
WGK Germany 3
HazardClass 9
PackingGroup III
HS Code 29242990
MSDS Information
ProviderLanguage
SigmaAldrich English
(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane Usage And Synthesis
Chemical PropertiesOff-White Solid
UsesAtazanavir intermediate. Enantiomer S
UsesIt function as a building block employed in the synthesis of HIV-1 protease inhibitors and is also employed in synthesizing (hydroxyethyl)urea peptidomimetrics and arylsulfonamides possessing anti-HIV activity. It is a Enantiomer S. Atazanavir intermediate.
(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane Preparation Products And Raw materials

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