tert-Butyl 4-nitrobenzylcarbamate
≥95%
- Product Code: 121418
CAS:
94838-58-1
| Molecular Weight: | 252.27 g./mol | Molecular Formula: | C₁₂H₁₆N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09038178 | |
| Melting Point: | Boiling Point: | 408.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a protective group for amines. It is often employed in peptide synthesis to safeguard the amine functionality during reactions, ensuring selective modification of other functional groups. The nitrobenzyl group can be removed under mild conditions, making it suitable for sensitive applications. Additionally, it serves as an intermediate in the preparation of pharmaceuticals and agrochemicals, where controlled release or protection of amine groups is critical. Its stability and ease of deprotection make it a valuable tool in complex synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White To Yellow To Light Green Powder Or Crystals |
| 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 | ฿910.00 |
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| 1.000 | 10-20 days | ฿1,800.00 |
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| 5.000 | 10-20 days | ฿5,720.00 |
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tert-Butyl 4-nitrobenzylcarbamate
This chemical is primarily utilized in organic synthesis as a protective group for amines. It is often employed in peptide synthesis to safeguard the amine functionality during reactions, ensuring selective modification of other functional groups. The nitrobenzyl group can be removed under mild conditions, making it suitable for sensitive applications. Additionally, it serves as an intermediate in the preparation of pharmaceuticals and agrochemicals, where controlled release or protection of amine groups is critical. Its stability and ease of deprotection make it a valuable tool in complex synthetic pathways.
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