Di-tert-butyl 4-amino-4-(3-(tert-butoxy)-3-oxopropyl)heptanedioate
95%
- Product Code: 46981
CAS:
136586-99-7
| Molecular Weight: | 415.5641 g./mol | Molecular Formula: | C₂₂H₄₁NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07357283 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and fine chemicals. Its structure, featuring multiple tert-butyl groups, makes it a valuable intermediate in protecting reactive functional groups during multi-step chemical reactions. It is often employed in the preparation of peptide-based drugs and other bioactive compounds, where selective protection and deprotection of functional groups are crucial. Additionally, it serves as a building block in the creation of specialized polymers and materials with tailored properties, such as controlled release systems or high-performance coatings. Its stability and compatibility with various reaction conditions make it a versatile tool in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,566.00 |
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Di-tert-butyl 4-amino-4-(3-(tert-butoxy)-3-oxopropyl)heptanedioate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and fine chemicals. Its structure, featuring multiple tert-butyl groups, makes it a valuable intermediate in protecting reactive functional groups during multi-step chemical reactions. It is often employed in the preparation of peptide-based drugs and other bioactive compounds, where selective protection and deprotection of functional groups are crucial. Additionally, it serves as a building block in the creation of specialized polymers and materials with tailored properties, such as controlled release systems or high-performance coatings. Its stability and compatibility with various reaction conditions make it a versatile tool in organic synthesis.
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