2,2'-Dibromo-1,1'-binaphthyl
≥96%
- Product Code: 115025
CAS:
74866-28-7
| Molecular Weight: | 412.12 g./mol | Molecular Formula: | C₂₀H₁₂Br₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00188005 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in the formation of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions. Its rigid binaphthyl structure provides a stable framework for inducing chirality in the resulting products, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it finds applications in material science, where its chiral properties are exploited in the development of advanced optical materials and liquid crystals.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White - Very Pale Yellow - Pale Reddish Yellow Or Pale Green Crystal - Powder |
| Purity (%) | 95.5-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿550.00 |
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| 0.200 | 10-20 days | ฿1,080.00 |
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| 1.000 | 10-20 days | ฿4,680.00 |
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2,2'-Dibromo-1,1'-binaphthyl
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in the formation of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and oxidation reactions. Its rigid binaphthyl structure provides a stable framework for inducing chirality in the resulting products, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it finds applications in material science, where its chiral properties are exploited in the development of advanced optical materials and liquid crystals.
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