(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane
95%
Reagent
Code: #58039
Alias
tert-butyl[(S)-1-[(S)-epoxypropyl-2-yl]-2-phenylethyl]carbamate; (2S,3S)-1,2-epoxy- 3-(tert-butyl-amino)-4-phenylbutane;[S-(R*,R*)]-(-)-(1-oxiranyl-2-phenylethyl)carbamate Butyl ester
CAS Number
98737-29-2
blur_circular Chemical Specifications
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Molecular Information
Weight
263.34 g/mol
Formula
C₁₅H₂₁NO₃
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Registry Numbers
EC Number
425-420-5
MDL Number
MFCD02258997
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Physical Properties
Melting Point
125-127 °C(lit.)
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Storage & Handling
Storage
room temperature, dry
description Product Description
This compound is primarily used in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. It serves as a key intermediate in the synthesis of peptides and peptidomimetics, where the Boc (tert-butoxycarbonyl) group acts as a protective group for amines. The epoxide ring in the structure allows for ring-opening reactions, enabling the formation of new carbon-nitrogen or carbon-oxygen bonds, which is crucial in constructing complex molecular frameworks. Its application is significant in drug discovery and development, especially in creating compounds with potential therapeutic effects.
format_list_bulleted Product Specification
| Test Parameter | Specification |
|---|---|
| Appearance | White to off-white solid |
| Purity | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
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