(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane CAS#: 98737-29-2

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

Basic information Safety Supplier Related

(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

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(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
solubility: soluble in Chloroform, Dichloromethane, Ethyl Acetate, Methanol
form: powder to crystal
pka: 12.19±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.
InChIKey: NVPOUMXZERMIJK-QWHCGFSZSA-N
CAS DataBase Reference: 98737-29-2(CAS DataBase Reference)

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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

Language:English Provider:SigmaAldrich

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

Chemical Properties

Off-White Solid

Uses

Atazanavir intermediate. Enantiomer S

Uses

It 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.

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