logo
Home  > Rac-2-(di-t-butylphosphino)-1,1'-binaphthyl

AB56269

255836-67-0 | Rac-2-(di-t-butylphosphino)-1,1'-binaphthyl

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $50.00 $35.00 -   +
1g 98% in stock $161.00 $113.00 -   +
10g 98% in stock $1,505.00 $1,054.00 -   +
25g 98% in stock $2,997.00 $2,098.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB56269
Chemical Name: Rac-2-(di-t-butylphosphino)-1,1'-binaphthyl
CAS Number: 255836-67-0
Molecular Formula: C28H31P
Molecular Weight: 398.51950099999993
MDL Number: MFCD03094576
SMILES: CC(P(C(C)(C)C)c1ccc2c(c1c1cccc3c1cccc3)cccc2)(C)C

 

Computed Properties
Complexity: 524  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 29  
Rotatable Bond Count: 4  
XLogP3: 7.6  

 

 

Upstream Synthesis Route
  • [1,1'-Binaphthalen]-2-yldi-tert-butylphosphine is a versatile and powerful reagent that finds extensive application in chemical synthesis. This compound is renowned for its ability to catalyze a wide range of organic reactions with high efficiency and selectivity. Due to its unique chiral framework, [1,1'-Binaphthalen]-2-yldi-tert-butylphosphine is particularly valuable in asymmetric synthesis, where the formation of molecules with specific stereochemistry is crucial.In organic synthesis, this compound has been successfully employed in various transformations, such as asymmetric hydrogenation, C-C bond formation, and conjugate additions. Its effectiveness in promoting these reactions can be attributed to its well-defined structure, which allows for precise control over the orientation of reacting molecules. Additionally, the tert-butyl substituents provide steric protection, enhancing the catalyst's stability and performance under harsh reaction conditions.Researchers and synthetic chemists rely on [1,1'-Binaphthalen]-2-yldi-tert-butylphosphine for the synthesis of complex molecules with high enantioselectivity. By harnessing the catalytic power of this compound, chemists can efficiently access a diverse array of chiral compounds for applications in pharmaceuticals, agrochemicals, and material science. The exceptional performance of [1,1'-Binaphthalen]-2-yldi-tert-butylphosphine underscores its indispensable role in modern chemical synthesis methodologies.
FEATURED PRODUCTS