logo
Home  > 2,2-Dibromo-1,1-binaphthyl

AB54423

74866-28-7 | 2,2-Dibromo-1,1-binaphthyl

Packsize Purity Availability Price Discounted Price    Quantity
1g >96.0%(GC) in stock $64.00 $45.00 -   +
5g >96.0%(GC) in stock $232.00 $162.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB54423
Chemical Name: 2,2-Dibromo-1,1-binaphthyl
CAS Number: 74866-28-7
Molecular Formula: C20H12Br2
Molecular Weight: 412.1173
MDL Number: MFCD00188005
SMILES: Brc1ccc2c(c1c1c(Br)ccc3c1cccc3)cccc2

 

Upstream Synthesis Route
  • 2,2'-Dibromo-1,1'-binaphthalene is a powerful chemical reagent that finds applications in various chemical synthesis processes. This compound is widely utilized as a chiral ligand in asymmetric catalysis reactions. Due to its unique structure and properties, 2,2'-Dibromo-1,1'-binaphthalene is particularly effective in promoting enantioselective transformations in organic synthesis.In metal-catalyzed reactions, 2,2'-Dibromo-1,1'-binaphthalene acts as a chiral ligand coordinating with metal centers to facilitate asymmetric transformations. These reactions lead to the formation of new chiral molecules with high optical purity. The ability of 2,2'-Dibromo-1,1'-binaphthalene to impart chirality to reaction intermediates makes it an invaluable tool in the production of pharmaceuticals, agrochemicals, and other fine chemicals.Furthermore, 2,2'-Dibromo-1,1'-binaphthalene has been employed in creating advanced materials with tailored properties. Its use in the synthesis of functionalized polymers and liquid crystals demonstrates its versatility in designing novel materials for various applications.Overall, 2,2'-Dibromo-1,1'-binaphthalene serves as a key component in the toolbox of synthetic chemists, enabling precise control over the stereochemical outcome of reactions and opening up new possibilities for the creation of complex organic molecules and advanced materials.
FEATURED PRODUCTS