352535-69-4 Usage
Description
(R)-(+)-N-CARBOMETHOXY-ALPHA, ALPHA-DIPHENYL-2-PYRROLIDINEMETHANOL, 98% is a high purity chemical compound, specifically an enantiomer of N-Carbomethoxy-Alpha, Alpha-Diphenyl-2-Pyrrolidinemethanol. It is widely utilized as a chiral auxiliary in organic synthesis and holds significant importance in the pharmaceutical industry and organic chemistry.
Uses
Used in Pharmaceutical Industry:
(R)-(+)-N-CARBOMETHOXY-ALPHA, ALPHA-DIPHENYL-2-PYRROLIDINEMETHANOL, 98% is used as a chiral auxiliary for the production of various drugs. Its high purity level ensures that it is suitable for creating high-quality pharmaceutical products.
Used in Organic Chemistry:
In the field of organic chemistry, (R)-(+)-N-CARBOMETHOXY-ALPHA, ALPHA-DIPHENYL-2-PYRROLIDINEMETHANOL, 98% is used for the synthesis of complex organic molecules. Its unique properties make it a valuable compound for creating intricate molecular structures.
Used in Research and Development:
(R)-(+)-N-CARBOMETHOXY-ALPHA, ALPHA-DIPHENYL-2-PYRROLIDINEMETHANOL, 98% is also employed in research, particularly in the development of new drugs and the study of chiral chemistry. Its high purity and enantiomeric nature make it an essential tool for advancing scientific understanding and creating innovative pharmaceutical solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 352535-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 352535-69:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*5)+(2*6)+(1*9)=144
144 % 10 = 4
So 352535-69-4 is a valid CAS Registry Number.
352535-69-4Relevant articles and documents
Lanthanide Lewis acid-mediated enantioselective conjugate radical additions
Sibi, Mukund P.,Manyem, Shankar
, p. 2929 - 2932 (2007/10/03)
(figure presented) Lanthanide triflates along with proline-derived ligands have been found to be efficient catalysts for enantioselective conjugate addition of nucleophilic radicals to enoates. N-Acyl oxazolidinones, when used as achiral additives, gave meaningful enhancements in the ees for the product.
