1-(tert-butyl)-3,4-dimethylcis-pyrrolidine-1,3,4-tricarboxylate
98%
- Product Code: 64499
| Molecular Weight: | 287.31 g./mol | Molecular Formula: | C₁₃H₂₁NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of complex molecules. Its structure, featuring multiple carboxylate groups and a tert-butyl moiety, makes it suitable for constructing pharmacologically active compounds, particularly in the synthesis of chiral pyrrolidine derivatives. These derivatives are often key components in the production of drugs targeting neurological and cardiovascular disorders. Additionally, the steric hindrance provided by the tert-butyl group enhances selectivity in chemical reactions, making it valuable in asymmetric synthesis. It is also employed in the preparation of ligands for catalytic systems, contributing to advancements in stereoselective transformations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,920.00 |
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| 1.000 | 10-20 days | ฿12,800.00 |
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| 5.000 | 10-20 days | ฿38,000.00 |
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| 10.000 | 10-20 days | ฿64,000.00 |
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1-(tert-butyl)-3,4-dimethylcis-pyrrolidine-1,3,4-tricarboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate for the development of complex molecules. Its structure, featuring multiple carboxylate groups and a tert-butyl moiety, makes it suitable for constructing pharmacologically active compounds, particularly in the synthesis of chiral pyrrolidine derivatives. These derivatives are often key components in the production of drugs targeting neurological and cardiovascular disorders. Additionally, the steric hindrance provided by the tert-butyl group enhances selectivity in chemical reactions, making it valuable in asymmetric synthesis. It is also employed in the preparation of ligands for catalytic systems, contributing to advancements in stereoselective transformations.
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