tert-Butyl (4-(oxazol-5-yl)benzyl)carbamate
97%
- Product Code: 36846
CAS:
1360616-36-9
| Molecular Weight: | 274.32 g./mol | Molecular Formula: | C₁₅H₁₈N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28965257 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in organic synthesis as a protective group for amines, particularly in peptide chemistry. The tert-butyloxycarbonyl (Boc) group safeguards the amine functionality during reactions, allowing selective transformations elsewhere in the molecule. It is also employed in the development of pharmaceuticals, where it helps in the synthesis of complex molecules by preventing unwanted side reactions. Additionally, its oxazole moiety can be utilized in the creation of heterocyclic compounds, which are often explored for their biological activity in drug discovery. The compound’s stability and ease of removal under mild acidic conditions make it a valuable tool in medicinal chemistry and biochemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,911.00 |
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| 0.250 | 10-20 days | ฿15,822.00 |
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tert-Butyl (4-(oxazol-5-yl)benzyl)carbamate
This compound is primarily used in organic synthesis as a protective group for amines, particularly in peptide chemistry. The tert-butyloxycarbonyl (Boc) group safeguards the amine functionality during reactions, allowing selective transformations elsewhere in the molecule. It is also employed in the development of pharmaceuticals, where it helps in the synthesis of complex molecules by preventing unwanted side reactions. Additionally, its oxazole moiety can be utilized in the creation of heterocyclic compounds, which are often explored for their biological activity in drug discovery. The compound’s stability and ease of removal under mild acidic conditions make it a valuable tool in medicinal chemistry and biochemical research.
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