tert-butyl [N'-(2-aminoethyl)-N-(tert-butoxycarbonyl)carbamimidoyl]carbamate (non-preferred name)
≥95%
- Product Code: 41351
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°C, inert gas |
Product Description:
This compound is primarily used in organic synthesis as a protecting group for amines, particularly in peptide synthesis. It helps to prevent unwanted reactions at the amine site during complex chemical processes. The tert-butoxycarbonyl (Boc) groups in the molecule provide stability under various reaction conditions, making it suitable for multi-step synthesis. It is also employed in the preparation of intermediates for pharmaceuticals and bioactive molecules, where selective protection and deprotection of functional groups are crucial. Additionally, its structure allows for controlled release of the protected amine under mild acidic conditions, ensuring precision in synthetic applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White To Yellow powder |
| 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 | Ft70,031.70 |
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-
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| 1.000 | 10-20 days | Ft189,085.60 |
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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 synthesis. It helps to prevent unwanted reactions at the amine site during complex chemical processes. The tert-butoxycarbonyl (Boc) groups in the molecule provide stability under various reaction conditions, making it suitable for multi-step synthesis. It is also employed in the preparation of intermediates for pharmaceuticals and bioactive molecules, where selective protection and deprotection of functional groups are crucial. Additionally, its structure allows for controlled release of the protected amine under mild acidic conditions, ensuring precision in synthetic applications.
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