tert-Butyl 4-aminophenethylcarbamate
98%
- Product Code: 72288
CAS:
94838-59-2
| Molecular Weight: | 236.31 g./mol | Molecular Formula: | C₁₃H₂₀N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring both an amino group and a carbamate moiety, makes it particularly valuable for constructing complex molecules, especially those targeting neurological and cardiovascular disorders. It is often employed in the synthesis of dopamine receptor agonists and other bioactive compounds that interact with the central nervous system. Additionally, its tert-butyl group provides steric protection, enabling selective reactions in multi-step synthetic pathways. This chemical is also explored in the development of prodrugs, where its carbamate functionality can be cleaved enzymatically to release active drug molecules in targeted therapeutic applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿880.00 |
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| 1.000 | 10-20 days | ฿2,300.00 |
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| 5.000 | 10-20 days | ฿6,980.00 |
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tert-Butyl 4-aminophenethylcarbamate
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals. Its structure, featuring both an amino group and a carbamate moiety, makes it particularly valuable for constructing complex molecules, especially those targeting neurological and cardiovascular disorders. It is often employed in the synthesis of dopamine receptor agonists and other bioactive compounds that interact with the central nervous system. Additionally, its tert-butyl group provides steric protection, enabling selective reactions in multi-step synthetic pathways. This chemical is also explored in the development of prodrugs, where its carbamate functionality can be cleaved enzymatically to release active drug molecules in targeted therapeutic applications.
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