(R)-3-tert-butyl 4-methyl 2,2-dimethyloxazolidine-3,4-dicarboxylate
97%
- Product Code: 229952
CAS:
95715-86-9
| Molecular Weight: | 259.30 g./mol | Molecular Formula: | C₁₂H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00674041 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a chiral auxiliary in asymmetric synthesis, this compound enables the stereoselective formation of complex organic molecules. Its rigid oxazolidine ring and defined stereochemistry help control the spatial arrangement during key bond-forming reactions, particularly in the synthesis of pharmaceuticals and bioactive compounds. It is often employed in aldol reactions, alkylations, and Diels-Alder cycloadditions where high enantioselectivity is required. After serving its directing role, the auxiliary can be cleaved under mild conditions, leaving the desired chiral product intact. Its tert-butyl and methyl ester groups enhance stability and solubility in common organic solvents, making it practical for multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿330.00 |
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| 5.000 | 10-20 days | ฿1,240.00 |
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| 25.000 | 10-20 days | ฿3,800.00 |
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| 100.000 | 10-20 days | ฿14,580.00 |
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(R)-3-tert-butyl 4-methyl 2,2-dimethyloxazolidine-3,4-dicarboxylate
Used as a chiral auxiliary in asymmetric synthesis, this compound enables the stereoselective formation of complex organic molecules. Its rigid oxazolidine ring and defined stereochemistry help control the spatial arrangement during key bond-forming reactions, particularly in the synthesis of pharmaceuticals and bioactive compounds. It is often employed in aldol reactions, alkylations, and Diels-Alder cycloadditions where high enantioselectivity is required. After serving its directing role, the auxiliary can be cleaved under mild conditions, leaving the desired chiral product intact. Its tert-butyl and methyl ester groups enhance stability and solubility in common organic solvents, making it practical for multi-step synthetic routes.
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