141096-35-7 Usage
Uses
Used in Pharmaceutical Industry:
(R)-2-(Diphenylphosphino)-1-phenylethylamine, min. 97% is used as a chiral ligand for [application reason] the synthesis of enantiomerically pure pharmaceutical compounds. Its ability to induce selectivity in catalytic reactions is crucial for producing single-enantiomer drugs, which can have significant impacts on the efficacy and safety of medications.
Used in Agrochemical Industry:
In the agrochemical industry, (R)-2-(Diphenylphosphino)-1-phenylethylamine, min. 97% is used as a ligand for [application reason] the development of chiral pesticides and other agrochemicals. (R)-2-(Diphenylphosphino)-1-phenylethylamine, min. 97%'s role in asymmetric catalysis helps in creating enantiomerically pure products, which can be more effective and have fewer side effects on non-target organisms.
Used in Fine Chemicals Production:
(R)-2-(Diphenylphosphino)-1-phenylethylamine, min. 97% is utilized as a key reagent in the synthesis of chiral fine chemicals for [application reason] various applications, including fragrances, flavors, and specialty chemicals. Its high purity ensures the quality and consistency of the final products.
Used in Chemical Research:
In the field of chemical research, (R)-2-(Diphenylphosphino)-1-phenylethylamine, min. 97% is employed as a research compound for [application reason] studying asymmetric catalysis and the development of new catalytic systems. Its specific stereochemistry makes it an ideal candidate for investigating the mechanisms of enantioselective reactions and for designing novel chiral catalysts.
Check Digit Verification of cas no
The CAS Registry Mumber 141096-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141096-35:
(8*1)+(7*4)+(6*1)+(5*0)+(4*9)+(3*6)+(2*3)+(1*5)=107
107 % 10 = 7
So 141096-35-7 is a valid CAS Registry Number.
141096-35-7Relevant academic research and scientific papers
Asymmetric Synthesis of Functionalised Pyrrolidines. Highly Diastereoselective Cyclisations Mediated by Sulfide and Sulfoxide Ligands
Davies, Ian W.,Gallagher, Timothy,Lamont, R. Brian,Scopes, David I.C.
, p. 335 - 337 (2007/10/02)
Silver(I)-catalysed cyclisation of sulfide 1b and sulfoxides 4 and 5 to give the corresponding 2-vinylpyrrolidines 2b, 6a and 7a, respectively proceeds with a high ( up to 99 percent diastereoisomeric excess) level of diastereoselectivity; in all of these
