(2S,5S)-2-tert-Butyl-3-methyl-5-(phenylmethyl)-4-imidazolidinone
≥95%,≥99%e.e.
- Product Code: 59686
CAS:
346440-54-8
| Molecular Weight: | 246.3 g./mol | Molecular Formula: | C₁₅H₂₂N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 93-100°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or catalyst. Its structure is particularly effective in facilitating enantioselective reactions, making it valuable in the production of pharmaceuticals and fine chemicals. The compound’s ability to induce high stereocontrol in reactions such as alkylations, aldol additions, and cyclizations is highly regarded. Additionally, it is employed in the development of novel drug candidates, where precise chiral induction is critical for achieving desired biological activity. Its use extends to academic research, where it aids in the study of stereochemistry and reaction mechanisms.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Light yellow powder to crystal |
| PURITY | 95-100 |
| MELTING POINT | 98.0-102.0 |
| Infrared spectrum | Conforms to Structure |
| Specific rotation a20DC1 MeOH | -58.0 -63.0 |
| e.e | 99 100% |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,320.00 |
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| 0.500 | 10-20 days | ฿13,200.00 |
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| 1.000 | 10-20 days | ฿19,800.00 |
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(2S,5S)-2-tert-Butyl-3-methyl-5-(phenylmethyl)-4-imidazolidinone
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or catalyst. Its structure is particularly effective in facilitating enantioselective reactions, making it valuable in the production of pharmaceuticals and fine chemicals. The compound’s ability to induce high stereocontrol in reactions such as alkylations, aldol additions, and cyclizations is highly regarded. Additionally, it is employed in the development of novel drug candidates, where precise chiral induction is critical for achieving desired biological activity. Its use extends to academic research, where it aids in the study of stereochemistry and reaction mechanisms.
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