tert-butyl [N'-(2-aminoethyl)-N-(tert-butoxycarbonyl)carbamimidoyl]carbamate (non-preferred name)
≥90% (HPLC)
- Product Code: 41350
CAS:
203258-44-0
| Molecular Weight: | 302.3699 g./mol | Molecular Formula: | C₁₃H₂₆N₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04974571 | |
| Melting Point: | 95-98℃ | Boiling Point: | |
| Density: | 1.137g/cm3 | Storage Condition: | -20℃, inert gas |
Product Description:
This compound is primarily used in organic synthesis as a protecting group for amines, particularly in peptide chemistry. It helps to prevent unwanted reactions at the amine site during complex synthetic processes. Its tert-butoxycarbonyl (Boc) groups are stable under various reaction conditions but can be selectively removed under acidic conditions, making it valuable for stepwise synthesis of peptides and other bioactive molecules. Additionally, it finds application in the preparation of intermediates for pharmaceuticals and agrochemicals due to its ability to protect functional groups while allowing other transformations to proceed.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,094.00 |
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| 1.000 | 10-20 days | ฿14,994.00 |
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tert-butyl [N'-(2-aminoethyl)-N-(tert-butoxycarbonyl)carbamimidoyl]carbamate (non-preferred name)
This compound is primarily used in organic synthesis as a protecting group for amines, particularly in peptide chemistry. It helps to prevent unwanted reactions at the amine site during complex synthetic processes. Its tert-butoxycarbonyl (Boc) groups are stable under various reaction conditions but can be selectively removed under acidic conditions, making it valuable for stepwise synthesis of peptides and other bioactive molecules. Additionally, it finds application in the preparation of intermediates for pharmaceuticals and agrochemicals due to its ability to protect functional groups while allowing other transformations to proceed.
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