(-)-10,2-Camphorsultam
98%
- Product Code: 62487
Alias:
(-)-10,2-camphorsultam
CAS:
94594-90-8
| Molecular Weight: | 215.31 g./mol | Molecular Formula: | C₁₀H₁₇NO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00066271 | |
| Melting Point: | 183-185 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
(-)-10,2-Camphorsultam is widely used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. It is highly effective in controlling stereochemistry during reactions such as alkylations, aldol additions, and Diels-Alder reactions, leading to products with high enantiomeric excess. Its rigid structure and ability to form stable complexes with metal catalysts make it valuable in enantioselective catalysis. Additionally, it is employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where precise chirality is critical for biological activity or desired properties. Its versatility and reliability in inducing asymmetry have established it as a key tool in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | WHITE TO LIGHT GREY POWDER |
| PURITYGC | 97.5 % 100 % |
| MELTING POINT | 182-185 |
| Infrared spectrum | Conforms to Structure |
| SOLUBILITY IN CHLOROFORM | ALMOST TRANSPARENCY |
| SPECIFIC ROTATION A20DC1CHCL3 | -30 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿310.00 |
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| 5.000 | 10-20 days | ฿630.00 |
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| 25.000 | 10-20 days | ฿2,410.00 |
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(-)-10,2-Camphorsultam
(-)-10,2-Camphorsultam is widely used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. It is highly effective in controlling stereochemistry during reactions such as alkylations, aldol additions, and Diels-Alder reactions, leading to products with high enantiomeric excess. Its rigid structure and ability to form stable complexes with metal catalysts make it valuable in enantioselective catalysis. Additionally, it is employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where precise chirality is critical for biological activity or desired properties. Its versatility and reliability in inducing asymmetry have established it as a key tool in organic synthesis.
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