(R)-3,3'-Dimethyl-[1,1'-binaphthalene]-2,2'-diol
≥98%,99%e.e.
- Product Code: 70304
CAS:
55515-98-5
| Molecular Weight: | 310.4 g./mol | Molecular Formula: | C₂₂H₁₈O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 201-202°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
(R)-3,3'-Dimethyl-[1,1'-binaphthalene]-2,2'-diol is widely used as a chiral ligand in asymmetric synthesis. It plays a crucial role in catalyzing enantioselective reactions, such as hydrogenation, oxidation, and carbon-carbon bond formation, enabling the production of optically active compounds. This chemical is particularly valuable in the pharmaceutical industry for synthesizing chiral drugs, where the correct enantiomer is essential for efficacy and safety. Additionally, it is employed in the development of advanced materials and organic electronics due to its ability to induce chirality in polymers and other complex molecules. Its robust and versatile nature makes it a key component in research and industrial applications requiring precise stereochemical control.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Off-white to light yellow Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $156.15 |
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| 0.250 | 10-20 days | $197.26 |
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| 1.000 | 10-20 days | $475.09 |
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(R)-3,3'-Dimethyl-[1,1'-binaphthalene]-2,2'-diol
(R)-3,3'-Dimethyl-[1,1'-binaphthalene]-2,2'-diol is widely used as a chiral ligand in asymmetric synthesis. It plays a crucial role in catalyzing enantioselective reactions, such as hydrogenation, oxidation, and carbon-carbon bond formation, enabling the production of optically active compounds. This chemical is particularly valuable in the pharmaceutical industry for synthesizing chiral drugs, where the correct enantiomer is essential for efficacy and safety. Additionally, it is employed in the development of advanced materials and organic electronics due to its ability to induce chirality in polymers and other complex molecules. Its robust and versatile nature makes it a key component in research and industrial applications requiring precise stereochemical control.
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