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R-3,3'-di-9-phenanthrenyl-1,1'-Binaphthalene]-2,2'-diol, commonly referred to as BINOL, is a chiral compound characterized by two naphthyl rings connected by a central carbon bridge. It is renowned for its role as a chiral ligand in asymmetric synthesis reactions and catalysis, especially in metal-catalyzed asymmetric transformations. BINOL's capacity to confer high enantioselectivity to a range of chemical reactions has established it as an indispensable tool in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, highlighting its versatility and significance in organic chemistry.

1058734-56-7

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1058734-56-7 Usage

Uses

Used in Pharmaceutical Industry:
R-3,3'-di-9-phenanthrenyl-1,1'-Binaphthalene]-2,2'-diol is used as a chiral ligand for enhancing the enantioselectivity of chemical reactions in the production of pharmaceuticals. Its ability to induce high selectivity is crucial for the synthesis of enantiomerically pure compounds, which are essential for the development of effective and safe drugs.
Used in Agrochemical Industry:
In the agrochemical sector, R-3,3'-di-9-phenanthrenyl-1,1'-Binaphthalene]-2,2'-diol serves as a chiral catalyst, facilitating asymmetric reactions to produce enantiomerically pure agrochemicals. This ensures the creation of active ingredients with targeted effects on pests, reducing the environmental impact and increasing the efficacy of these products.
Used in Fine Chemicals Industry:
R-3,3'-di-9-phenanthrenyl-1,1'-Binaphthalene]-2,2'-diol is utilized as a chiral building block in the synthesis of fine chemicals. Its unique structure allows for the creation of complex molecules with specific stereochemistry, which is vital for the development of high-quality fragrances, flavors, and other specialty chemicals.
Used in Asymmetric Synthesis Research:
In the field of organic chemistry research, R-3,3'-di-9-phenanthrenyl-1,1'-Binaphthalene]-2,2'-diol is employed as a model compound for studying asymmetric synthesis and catalysis. Its well-defined structure and reactivity provide insights into the mechanisms of enantioselective reactions and contribute to the advancement of synthetic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 1058734-56-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,8,7,3 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1058734-56:
(9*1)+(8*0)+(7*5)+(6*8)+(5*7)+(4*3)+(3*4)+(2*5)+(1*6)=167
167 % 10 = 7
So 1058734-56-7 is a valid CAS Registry Number.

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