tert-Butyl (23-hydroxy-3,6,9,12,15,18,21-heptaoxatricosyl)carbamate
95%
- Product Code: 61602
CAS:
1345337-22-5
| Molecular Weight: | 469.57 g./mol | Molecular Formula: | C₂₁H₄₃NO₁₀ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28976659 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of drug development and medicinal chemistry. It serves as a protective group for amines during multi-step synthetic processes, ensuring selective reactions without unwanted side interactions. Its structure, featuring a long polyether chain, enhances solubility in various solvents, making it suitable for reactions in both organic and aqueous environments. Additionally, it is employed in the preparation of peptide-based therapeutics, where its stability under mild conditions allows for efficient deprotection without disrupting the peptide backbone. Its applications also extend to the development of advanced materials, such as polymers and dendrimers, where its functional groups enable precise modifications and controlled assembly.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿6,570.00 |
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| 1.000 | 10-20 days | ฿16,416.00 |
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| 5.000 | 10-20 days | ฿57,447.00 |
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tert-Butyl (23-hydroxy-3,6,9,12,15,18,21-heptaoxatricosyl)carbamate
This chemical is primarily utilized in the synthesis of complex organic molecules, particularly in the field of drug development and medicinal chemistry. It serves as a protective group for amines during multi-step synthetic processes, ensuring selective reactions without unwanted side interactions. Its structure, featuring a long polyether chain, enhances solubility in various solvents, making it suitable for reactions in both organic and aqueous environments. Additionally, it is employed in the preparation of peptide-based therapeutics, where its stability under mild conditions allows for efficient deprotection without disrupting the peptide backbone. Its applications also extend to the development of advanced materials, such as polymers and dendrimers, where its functional groups enable precise modifications and controlled assembly.
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