122709-72-2 Usage
Uses
Used in Pharmaceutical Development:
1-Pyrrolidinecarboxamide,4-(dicyclohexylphosphino)-2-[(diphenylphosphino)methyl]-N-methyl-,(2R,4R)is used as a chiral ligand in the pharmaceutical industry for its ability to selectively produce specific enantiomers. This selective production is crucial for the development of drugs with desired therapeutic effects and reduced side effects.
Used in Agrochemical Production:
In the agrochemical industry, 1-Pyrrolidinecarboxamide,4-(dicyclohexylphosphino)-2-[(diphenylphosphino)methyl]-N-methyl-,(2R,4R)is employed as a chiral ligand for the synthesis of enantiomerically pure agrochemicals. This ensures the effectiveness and safety of these products, as only the desired enantiomer is produced.
Used in Fine Chemicals and Materials Production:
1-Pyrrolidinecarboxamide,4-(dicyclohexylphosphino)-2-[(diphenylphosphino)methyl]-N-methyl-,(2R,4R)is used as a chiral ligand in the production of fine chemicals and materials. Its unique structure and properties contribute to the development of high-quality and specialized products in various industries, such as fragrances, dyes, and advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 122709-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,7,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122709-72:
(8*1)+(7*2)+(6*2)+(5*7)+(4*0)+(3*9)+(2*7)+(1*2)=112
112 % 10 = 2
So 122709-72-2 is a valid CAS Registry Number.
122709-72-2Relevant academic research and scientific papers
Efficient asymmetric hydrogenation of α-amino ketone derivatives. A highly enantioselective synthesis of phenylephrine, levamisole, carnitine and propranolol
Sukuraba,Takahashi,Takeda,Achiwa
, p. 738 - 747 (2007/10/02)
The complexes of pyrrolidine bisphosphine ligands (CPMs) with rhodium (I) were found to be efficient catalysts for asymmetric hydrogenation of α-amino ketone hydrochloride derivatives. Utilizing this methodology, we have developed efficient asymmetric syntheses of the optically active β-amino alcohols, phenylephrine, levamisole, carnitine and propranolol.
