(R)-2,2'-Dimethyl-1,1'-binaphthyl
≥98%
- Product Code: 70289
CAS:
19634-89-0
| Molecular Weight: | 282.39 g./mol | Molecular Formula: | C₂₂H₁₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00048075 | |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions, to produce chiral molecules with high enantiomeric purity. Its rigid binaphthyl structure provides excellent steric and electronic control, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a key component in chiral catalysts and reagents, enabling the production of optically active compounds in industrial and academic research settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | £162.44 |
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(R)-2,2'-Dimethyl-1,1'-binaphthyl
This compound is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions, to produce chiral molecules with high enantiomeric purity. Its rigid binaphthyl structure provides excellent steric and electronic control, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a key component in chiral catalysts and reagents, enabling the production of optically active compounds in industrial and academic research settings.
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