tert-Butyl 1-benzyl-2-(methoxy(methyl)amino)-2-oxoethylcarbamate
95%
- Product Code: 82813
CAS:
184711-70-4
| Molecular Weight: | 308.37 g./mol | Molecular Formula: | C₁₆H₂₄N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24390019 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a protected intermediate for the preparation of peptides and other biologically active compounds. Its structure, featuring a tert-butyl carbamate group, allows it to act as a protecting group for amines, ensuring selective reactions during complex synthetic processes. The methoxy(methyl)amino moiety enhances its stability and reactivity, making it suitable for use in multi-step synthesis, particularly in pharmaceutical research and development. It is often employed in the synthesis of complex molecules, including potential drug candidates, where precise control over functional groups is critical. Additionally, its benzyl group provides further versatility in chemical transformations, enabling its use in the construction of diverse molecular architectures.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,020.00 |
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| 0.250 | 10-20 days | ฿11,700.00 |
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| 1.000 | 10-20 days | ฿23,400.00 |
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tert-Butyl 1-benzyl-2-(methoxy(methyl)amino)-2-oxoethylcarbamate
This chemical is primarily utilized in organic synthesis as a protected intermediate for the preparation of peptides and other biologically active compounds. Its structure, featuring a tert-butyl carbamate group, allows it to act as a protecting group for amines, ensuring selective reactions during complex synthetic processes. The methoxy(methyl)amino moiety enhances its stability and reactivity, making it suitable for use in multi-step synthesis, particularly in pharmaceutical research and development. It is often employed in the synthesis of complex molecules, including potential drug candidates, where precise control over functional groups is critical. Additionally, its benzyl group provides further versatility in chemical transformations, enabling its use in the construction of diverse molecular architectures.
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