(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane
95%
- Product 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:
98737-29-2
| Molecular Weight: | 263.34 g./mol | Molecular Formula: | C₁₅H₂₁NO₃ |
|---|---|---|---|
| EC Number: | 425-420-5 | MDL Number: | MFCD02258997 |
| Melting Point: | 125-127 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
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.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off white solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿300.00 |
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| 1.000 | 10-20 days | ฿620.00 |
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| 5.000 | 10-20 days | ฿1,810.00 |
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| 25.000 | 10-20 days | ฿5,180.00 |
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| 100.000 | 10-20 days | ฿15,520.00 |
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| 500.000 | 10-20 days | ฿46,580.00 |
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(2S,3S)-1,2-Epoxy-3-(Boc-amino)-4-phenylbutane
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.
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