(S)-6,6'-Dibromo-2,2'-dimethoxy-1,1'-binaphthalene
95%
- Product Code: 37991
CAS:
117745-41-2
| Molecular Weight: | 472.1700 g./mol | Molecular Formula: | C₂₂H₁₆Br₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06654379 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a binaphthalene core with methoxy and bromo substituents, makes it effective in inducing chirality in catalytic reactions. It is often employed in enantioselective transformations, such as hydrogenation, oxidation, and carbon-carbon bond-forming reactions, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, it serves as a building block for constructing more complex chiral frameworks used in advanced material science and organic electronics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $70.08 |
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(S)-6,6'-Dibromo-2,2'-dimethoxy-1,1'-binaphthalene
This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a binaphthalene core with methoxy and bromo substituents, makes it effective in inducing chirality in catalytic reactions. It is often employed in enantioselective transformations, such as hydrogenation, oxidation, and carbon-carbon bond-forming reactions, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, it serves as a building block for constructing more complex chiral frameworks used in advanced material science and organic electronics.
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