(R)-3,3'-Dibromo-bis(methoxymethoxyl)-1,1'-binaphtyl
≥98%,99%e.e.
- Product Code: 70303
CAS:
211734-49-5
| Molecular Weight: | 532.2 g./mol | Molecular Formula: | C₂₄H₂₀Br₂O₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 123-124°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in catalytic reactions. It plays a significant role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic reactions where high stereochemical control is required. Its application is crucial in the pharmaceutical industry for the production of chiral drugs, ensuring the desired enantiomer is obtained with high purity. Additionally, it is employed in academic research to develop and optimize new catalytic methodologies, contributing to advancements in synthetic organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $46.49 |
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| 1.000 | 10-20 days | $182.17 |
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(R)-3,3'-Dibromo-bis(methoxymethoxyl)-1,1'-binaphtyl
This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in catalytic reactions. It plays a significant role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic reactions where high stereochemical control is required. Its application is crucial in the pharmaceutical industry for the production of chiral drugs, ensuring the desired enantiomer is obtained with high purity. Additionally, it is employed in academic research to develop and optimize new catalytic methodologies, contributing to advancements in synthetic organic chemistry.
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