tert-Butyl (4-(methoxy(methyl)amino)-4-oxobutyl)carbamate
95%
- Product Code: 83834
CAS:
227751-84-0
| Molecular Weight: | 246.30 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23702195 | |
| Melting Point: | 42-43 °C | Boiling Point: | |
| Density: | 1.056±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both a carbamate and an amide group, makes it suitable for constructing complex molecules, particularly in pharmaceutical research. The tert-butyl group provides steric protection, allowing selective reactions at other functional sites. It is often employed in peptide synthesis, where it serves as a protecting group for amines, ensuring controlled deprotection and minimizing side reactions. Additionally, its methoxy(methyl)amino moiety can act as a precursor for introducing specific functional groups into target molecules, enhancing their biological activity or stability. Its role in medicinal chemistry includes the development of drug candidates, particularly in the synthesis of protease inhibitors and other biologically active compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,646.00 |
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| 0.250 | 10-20 days | ฿4,428.00 |
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| 1.000 | 10-20 days | ฿8,856.00 |
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tert-Butyl (4-(methoxy(methyl)amino)-4-oxobutyl)carbamate
This compound is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both a carbamate and an amide group, makes it suitable for constructing complex molecules, particularly in pharmaceutical research. The tert-butyl group provides steric protection, allowing selective reactions at other functional sites. It is often employed in peptide synthesis, where it serves as a protecting group for amines, ensuring controlled deprotection and minimizing side reactions. Additionally, its methoxy(methyl)amino moiety can act as a precursor for introducing specific functional groups into target molecules, enhancing their biological activity or stability. Its role in medicinal chemistry includes the development of drug candidates, particularly in the synthesis of protease inhibitors and other biologically active compounds.
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