N-[(11bR)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-oxido-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,1,1-trifluoromethanesulfonamide
≥98%,≥99% e.e.
- Product Code: 57501
CAS:
1010800-02-8
| Molecular Weight: | 903.6 g./mol | Molecular Formula: | C₃₇H₁₇F₁₅NO₅PS |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 740.7±70.0 °C | |
| Density: | 1.70±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in advanced organic synthesis, particularly in asymmetric catalysis. Its structure, featuring trifluoromethyl groups and a phosphine oxide moiety, makes it highly effective as a chiral ligand or catalyst in enantioselective reactions. It is often employed in the synthesis of complex pharmaceutical intermediates, where high stereochemical control is required. Additionally, its electron-withdrawing groups enhance its stability and reactivity in challenging chemical environments, making it suitable for use in the development of fine chemicals and specialty materials. Its application extends to the field of agrochemicals, where it aids in the creation of optically active compounds with improved efficacy.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Solid |
| PURITY | 98-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,810.00 |
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| 0.250 | 10-20 days | ฿10,650.00 |
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N-[(11bR)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-oxido-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,1,1-trifluoromethanesulfonamide
This chemical is primarily utilized in advanced organic synthesis, particularly in asymmetric catalysis. Its structure, featuring trifluoromethyl groups and a phosphine oxide moiety, makes it highly effective as a chiral ligand or catalyst in enantioselective reactions. It is often employed in the synthesis of complex pharmaceutical intermediates, where high stereochemical control is required. Additionally, its electron-withdrawing groups enhance its stability and reactivity in challenging chemical environments, making it suitable for use in the development of fine chemicals and specialty materials. Its application extends to the field of agrochemicals, where it aids in the creation of optically active compounds with improved efficacy.
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