(S)-3,3'-Dibromo-2,2'-dimethoxy-1,1'-binaphthyl
98.0%
- Product Code: 66361
CAS:
75714-60-2
| Molecular Weight: | 472.18 g./mol | Molecular Formula: | C₂₂H₁₆Br₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04038415 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a significant role in the formation of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the development of drugs with specific chiral configurations. Its structure allows it to effectively coordinate with metal catalysts, enhancing the selectivity and efficiency of reactions such as hydrogenation, carbon-carbon bond formation, and oxidation processes. Additionally, it is employed in the synthesis of complex organic molecules, contributing to advancements in material science and fine chemical production. Its chiral properties make it a valuable tool in research and industrial applications where precise stereochemical control is required.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 180 185? |
| PurityGC | 98 100% |
| SPECIFIC ROTATION A20DC1 CHCL3 | -10 0 |
| INFRARED SPECTROMETRY | Conforms to Structure |
| SOLUBILITY IN CHLOROFORM | almost transparency |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,159.00 |
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| 1.000 | 10-20 days | ฿7,011.00 |
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(S)-3,3'-Dibromo-2,2'-dimethoxy-1,1'-binaphthyl
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a significant role in the formation of enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the development of drugs with specific chiral configurations. Its structure allows it to effectively coordinate with metal catalysts, enhancing the selectivity and efficiency of reactions such as hydrogenation, carbon-carbon bond formation, and oxidation processes. Additionally, it is employed in the synthesis of complex organic molecules, contributing to advancements in material science and fine chemical production. Its chiral properties make it a valuable tool in research and industrial applications where precise stereochemical control is required.
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| Stable in pH range | - |
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