N-[(11bR)-2,6-Di-9-anthracenyl-8,9,10,11,12,13,14,15-octahydro-8-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,1,1-trifluoromethanesulfonamide
≥98%,≥99% e.e.
- Product Code: 57513
CAS:
1227374-65-3
| Molecular Weight: | 839.9 g./mol | Molecular Formula: | C₄₉H₃₇F₃NO₅PS |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | 1.49±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis and catalysis. It serves as a highly effective chiral ligand in asymmetric catalytic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure and steric properties make it valuable for controlling the stereochemistry of complex organic transformations, such as hydrogenation, carbon-carbon bond formation, and other pivotal reactions in pharmaceutical and fine chemical production. Additionally, its trifluoromethanesulfonamide moiety enhances its stability and reactivity, making it suitable for use in demanding reaction conditions. Its application is particularly significant in the development of chiral drugs and intermediates, where precise stereocontrol is critical.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $741.69 |
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N-[(11bR)-2,6-Di-9-anthracenyl-8,9,10,11,12,13,14,15-octahydro-8-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,1,1-trifluoromethanesulfonamide
This compound is primarily utilized in the field of organic synthesis and catalysis. It serves as a highly effective chiral ligand in asymmetric catalytic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure and steric properties make it valuable for controlling the stereochemistry of complex organic transformations, such as hydrogenation, carbon-carbon bond formation, and other pivotal reactions in pharmaceutical and fine chemical production. Additionally, its trifluoromethanesulfonamide moiety enhances its stability and reactivity, making it suitable for use in demanding reaction conditions. Its application is particularly significant in the development of chiral drugs and intermediates, where precise stereocontrol is critical.
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