(2R,3R)-3-(tert-Butyl)-4-(2,6-dimethoxyphenyl)-2-isopropyl-2,3-dihydrobenzo[d][1,3]oxaphosphole
97%
- Product Code: 36472
CAS:
1477517-19-3
Molecular Weight: | 372.4300 g./mol | Molecular Formula: | C₂₂H₂₉O₃P |
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EC Number: | MDL Number: | MFCD32206570 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. The presence of the tert-butyl and isopropyl groups enhances steric control, improving selectivity in producing chiral molecules. This compound is valuable in pharmaceutical research for synthesizing enantiomerically pure drugs, where chirality plays a critical role in biological activity. Additionally, it may find use in material science for developing chiral polymers or advanced catalytic systems.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿4,122.00 |
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(2R,3R)-3-(tert-Butyl)-4-(2,6-dimethoxyphenyl)-2-isopropyl-2,3-dihydrobenzo[d][1,3]oxaphosphole
This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a dihydrobenzo[d][1,3]oxaphosphole core, makes it effective in facilitating enantioselective transformations, such as hydrogenation or carbon-carbon bond-forming reactions. The presence of the tert-butyl and isopropyl groups enhances steric control, improving selectivity in producing chiral molecules. This compound is valuable in pharmaceutical research for synthesizing enantiomerically pure drugs, where chirality plays a critical role in biological activity. Additionally, it may find use in material science for developing chiral polymers or advanced catalytic systems.
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