(11bS)-2,6-Bis[bis[3,5-bis(trifluoromethyl)phenyl]hydroxymethyl]-3,5-dihydrospiro[4H-dinaphth[2,1-c:1',2'-e]azepine-4,4'-morpholinium] Bromide
97%
- Product Code: 73111
CAS:
1197922-04-5
| Molecular Weight: | 1354.82 g./mol | Molecular Formula: | C₆₀H₃₆BrF₂₄NO₃ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and catalysis, particularly in asymmetric reactions. Its unique structure, featuring multiple trifluoromethyl groups and a spirocyclic framework, makes it highly effective as a chiral catalyst or ligand. It is often employed in enantioselective transformations, such as hydrogenation, cyclization, or cross-coupling reactions, where high stereocontrol is required. The presence of electron-withdrawing trifluoromethyl groups enhances its reactivity and selectivity in complex organic reactions. Additionally, its stability and solubility in various organic solvents make it suitable for use in industrial-scale chemical processes, particularly in the pharmaceutical industry for the synthesis of chiral drug intermediates.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿9,360.00 |
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| 0.050 | 10-20 days | ฿29,800.00 |
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(11bS)-2,6-Bis[bis[3,5-bis(trifluoromethyl)phenyl]hydroxymethyl]-3,5-dihydrospiro[4H-dinaphth[2,1-c:1',2'-e]azepine-4,4'-morpholinium] Bromide
This chemical is primarily utilized in the field of organic synthesis and catalysis, particularly in asymmetric reactions. Its unique structure, featuring multiple trifluoromethyl groups and a spirocyclic framework, makes it highly effective as a chiral catalyst or ligand. It is often employed in enantioselective transformations, such as hydrogenation, cyclization, or cross-coupling reactions, where high stereocontrol is required. The presence of electron-withdrawing trifluoromethyl groups enhances its reactivity and selectivity in complex organic reactions. Additionally, its stability and solubility in various organic solvents make it suitable for use in industrial-scale chemical processes, particularly in the pharmaceutical industry for the synthesis of chiral drug intermediates.
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