tert-Butyl (2-(2-(2-(2-bromoethoxy)ethoxy)ethoxy)ethyl)carbamate
97%
- Product Code: 113062
CAS:
1076199-21-7
| Molecular Weight: | 356.25 g./mol | Molecular Formula: | C₁₃H₂₆BrNO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09840081 | |
| Melting Point: | Boiling Point: | 422.1±35.0°C at 3 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the creation of complex molecules. It serves as a versatile intermediate in the development of pharmaceuticals, where its structure allows for the introduction of functional groups or the formation of specific bonds. The presence of the bromoethoxy chain makes it valuable in constructing polyethylene glycol (PEG)-like linkers, which are often used in drug delivery systems to enhance solubility and bioavailability. Additionally, its carbamate group provides a protective moiety for amines during multi-step synthetic processes, ensuring selective reactivity in the synthesis of peptides or other bioactive compounds.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Colorless To Light Yellow Liquid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $105.47 |
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| 0.250 | 10-20 days | $168.76 |
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tert-Butyl (2-(2-(2-(2-bromoethoxy)ethoxy)ethoxy)ethyl)carbamate
This chemical is primarily utilized in organic synthesis, particularly in the creation of complex molecules. It serves as a versatile intermediate in the development of pharmaceuticals, where its structure allows for the introduction of functional groups or the formation of specific bonds. The presence of the bromoethoxy chain makes it valuable in constructing polyethylene glycol (PEG)-like linkers, which are often used in drug delivery systems to enhance solubility and bioavailability. Additionally, its carbamate group provides a protective moiety for amines during multi-step synthetic processes, ensuring selective reactivity in the synthesis of peptides or other bioactive compounds.
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