S-3,3'-bis[4-(2-naphthalenyl)phenyl]-1,1'-Binaphthalene]-2,2'-diol, also known as BNBP, is a chiral diol compound with a complex molecular structure. It belongs to the family of binaphthalene derivatives and is often used as a chiral ligand in asymmetric synthesis and catalysis. BNBP has been employed in various organic reactions and has shown to be effective in promoting enantioselective processes. Its unique structure and stereochemistry make it an important tool in the field of organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, its ability to form stable complexes with metal ions makes it valuable in the development of new catalytic systems. Used in Pharmaceutical Industry: S-3,3'-bis[4-(2-naphthalenyl)phenyl]-1,1'-Binaphthalene]-2,2'-diol is used as a chiral ligand for asymmetric synthesis and catalysis in the production of pharmaceuticals. Its unique structure and stereochemistry enable the production of enantiomerically pure compounds, which are essential for the development of effective and safe drugs. Used in Agrochemical Industry: S-3,3'-bis[4-(2-naphthalenyl)phenyl]-1,1'-Binaphthalene]-2,2'-diol is used as a chiral ligand for asymmetric synthesis and catalysis in the production of agrochemicals. Its ability to promote enantioselective processes helps in the development of more effective and environmentally friendly pesticides and other agricultural products. Used in Fine Chemicals Industry: S-3,3'-bis[4-(2-naphthalenyl)phenyl]-1,1'-Binaphthalene]-2,2'-diol is used as a chiral ligand for asymmetric synthesis and catalysis in the production of fine chemicals. Its unique structure and stereochemistry make it an important tool for the synthesis of high-quality and enantiomerically pure compounds used in various applications, such as fragrances, dyes, and specialty chemicals. Used in Catalysis Research: S-3,3'-bis[4-(2-naphthalenyl)phenyl]-1,1'-Binaphthalene]-2,2'-diol is used as a chiral ligand in the development of new catalytic systems. Its ability to form stable complexes with metal ions makes it valuable for the design and synthesis of novel catalysts that can improve the efficiency and selectivity of various chemical reactions.
The CAS Registry Mumber 309934-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,9,9,3 and 4 respectively; the second part has 2 digits, 8 and 7 respectively. Calculate Digit Verification of CAS Registry Number 309934-87: (8*3)+(7*0)+(6*9)+(5*9)+(4*3)+(3*4)+(2*8)+(1*7)=170 170 % 10 = 0 So 309934-87-0 is a valid CAS Registry Number.
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