(-)-Benzotetramisole
98.0%
- Product Code: 70783
Alias:
(2S)-2,3-Dihydro-2-phenylimidazo[2,1-b]benzothiazole
CAS:
950194-37-3
| Molecular Weight: | 252.34 g./mol | Molecular Formula: | C₁₅H₁₂N₂S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized as a chiral catalyst in asymmetric organic synthesis, particularly in the enantioselective reactions of carbonyl compounds. It is highly effective in promoting the kinetic resolution of secondary alcohols and the desymmetrization of meso-anhydrides, making it valuable in the production of optically active intermediates for pharmaceuticals and fine chemicals. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, where high enantiomeric purity is essential. Its robust catalytic activity and selectivity make it a preferred choice in academic research and industrial applications for developing chiral compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Very pale yellow Crystal - Powder |
| PURITY | 98-100 |
| MELTING POINT | 93-97 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,800.00 |
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| 1.000 | 10-20 days | ฿6,300.00 |
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| 5.000 | 10-20 days | ฿21,680.00 |
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(-)-Benzotetramisole
This compound is primarily utilized as a chiral catalyst in asymmetric organic synthesis, particularly in the enantioselective reactions of carbonyl compounds. It is highly effective in promoting the kinetic resolution of secondary alcohols and the desymmetrization of meso-anhydrides, making it valuable in the production of optically active intermediates for pharmaceuticals and fine chemicals. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, where high enantiomeric purity is essential. Its robust catalytic activity and selectivity make it a preferred choice in academic research and industrial applications for developing chiral compounds.
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