959864-39-2 Usage
Description
Tetramethyl 6,6'-bis(diphenylphosphanyl)-1,1',3,3'-tetrahydro-2H,2'H-[5,5'-biindene]-2,2,2',2'-tetracarboxylate is a complex organic compound featuring a tetrahydro-biindene core with diphenylphosphanyl groups and tetramethyl carboxylate substituents. This molecule is characterized by its unique structure and potential applications in chemical reactions and catalysis.
Uses
Used in Chemical Synthesis:
Tetramethyl 6,6'-bis(diphenylphosphanyl)-1,1',3,3'-tetrahydro-2H,2'H-[5,5'-biindene]-2,2,2',2'-tetracarboxylate is used as a ligand in the platinum-catalyzed asymmetric carbonyl-ene reaction. This reaction is an important method for the synthesis of chiral compounds, which are crucial in the pharmaceutical and agrochemical industries. The ligand's unique structure allows for the selective formation of enantioenriched products, enhancing the efficiency and selectivity of the reaction.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, tetramethyl 6,6'-bis(diphenylphosphanyl)-1,1',3,3'-tetrahydro-2H,2'H-[5,5'-biindene]-2,2,2',2'-tetracarboxylate is used as a chiral ligand for the synthesis of enantiomerically pure compounds. The ability to produce chiral compounds with high selectivity is essential for the development of new drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, tetramethyl 6,6'-bis(diphenylphosphanyl)-1,1',3,3'-tetrahydro-2H,2'H-[5,5'-biindene]-2,2,2',2'-tetracarboxylate is employed as a chiral ligand for the synthesis of enantioselective agrochemicals. This allows for the development of more effective and environmentally friendly pesticides and herbicides.
Used in Research and Development:
Tetramethyl 6,6'-bis(diphenylphosphanyl)-1,1',3,3'-tetrahydro-2H,2'H-[5,5'-biindene]-2,2,2',2'-tetracarboxylate is also used in research and development for the study of asymmetric catalysis and the development of new synthetic methods. Its unique structure and reactivity make it a valuable tool for understanding the mechanisms of enantioselective reactions and for designing new catalysts and ligands.
Check Digit Verification of cas no
The CAS Registry Mumber 959864-39-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,9,8,6 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 959864-39:
(8*9)+(7*5)+(6*9)+(5*8)+(4*6)+(3*4)+(2*3)+(1*9)=252
252 % 10 = 2
So 959864-39-2 is a valid CAS Registry Number.