(S)-()-(2-Methylacryloyl)-2,10-camphorsultam
99%
- Product Code: 62506
CAS:
128441-99-6
| Molecular Weight: | 283.39 g./mol | Molecular Formula: | C₁₄H₂₁NO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30530176 | |
| Melting Point: | Boiling Point: | 397.5±25.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Widely used in asymmetric synthesis, particularly in the preparation of chiral compounds. It serves as a key chiral auxiliary in organic reactions, enabling the formation of enantiomerically pure products. Commonly employed in the synthesis of pharmaceuticals, where precise stereochemistry is crucial for drug efficacy and safety. Its application extends to the production of fine chemicals and specialty materials that require high enantiomeric purity. Additionally, it is utilized in academic research for developing new methodologies in asymmetric catalysis and stereoselective transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿864.00 |
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| 1.000 | 10-20 days | ฿2,106.00 |
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| 5.000 | 10-20 days | ฿6,156.00 |
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(S)-()-(2-Methylacryloyl)-2,10-camphorsultam
Widely used in asymmetric synthesis, particularly in the preparation of chiral compounds. It serves as a key chiral auxiliary in organic reactions, enabling the formation of enantiomerically pure products. Commonly employed in the synthesis of pharmaceuticals, where precise stereochemistry is crucial for drug efficacy and safety. Its application extends to the production of fine chemicals and specialty materials that require high enantiomeric purity. Additionally, it is utilized in academic research for developing new methodologies in asymmetric catalysis and stereoselective transformations.
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