tert-Butyl (3-aminopropyl)(3-((tert-butoxycarbonyl)amino)propyl)carbamate
95%
- Product Code: 152294
CAS:
122248-82-2
| Molecular Weight: | 331.45 g./mol | Molecular Formula: | C₁₆H₃₃N₃O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12408086 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used primarily as a protected diamine building block in organic synthesis, especially in peptide and pharmaceutical manufacturing. Its main application lies in stepwise construction of complex amine-containing molecules where selective protection is critical. The Boc (tert-butoxycarbonyl) groups allow for controlled deprotection under mild acidic conditions, enabling the sequential addition of amino acids or other functional groups without side reactions. Commonly employed in solid-phase and solution-phase synthesis of bioactive compounds, including drug intermediates and heterocycles. Its symmetrical spacer structure with two protected amine ends makes it valuable for designing linkers, dendrimers, and bifunctional molecules in medicinal chemistry.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,500.00 |
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| 0.250 | 10-20 days | ฿4,950.00 |
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tert-Butyl (3-aminopropyl)(3-((tert-butoxycarbonyl)amino)propyl)carbamate
Used primarily as a protected diamine building block in organic synthesis, especially in peptide and pharmaceutical manufacturing. Its main application lies in stepwise construction of complex amine-containing molecules where selective protection is critical. The Boc (tert-butoxycarbonyl) groups allow for controlled deprotection under mild acidic conditions, enabling the sequential addition of amino acids or other functional groups without side reactions. Commonly employed in solid-phase and solution-phase synthesis of bioactive compounds, including drug intermediates and heterocycles. Its symmetrical spacer structure with two protected amine ends makes it valuable for designing linkers, dendrimers, and bifunctional molecules in medicinal chemistry.
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