7005-20-1 Usage
Uses
Used in Pharmaceutical Industry:
(2R)-pyrrolidine-2-carboxylic acid is used as a building block for the synthesis of various pharmaceutical compounds due to its unique cyclic structure and ability to form specific bonds with other amino acids.
Used in Nutritional Supplements:
(2R)-pyrrolidine-2-carboxylic acid is used as a dietary supplement to support collagen production, immune response, wound healing, and overall health and well-being.
Used in Cosmetics Industry:
(2R)-pyrrolidine-2-carboxylic acid is used as an ingredient in cosmetic products to promote skin health and collagen production, contributing to the maintenance of skin elasticity and firmness.
Used in Food and Beverage Industry:
(2R)-pyrrolidine-2-carboxylic acid is used as a flavor enhancer and a building block for the synthesis of other flavor compounds in the food and beverage industry.
Used in Research and Development:
(2R)-pyrrolidine-2-carboxylic acid is used as a research tool in the development of new drugs, therapies, and applications due to its unique properties and potential health benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 7005-20-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,0 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7005-20:
(6*7)+(5*0)+(4*0)+(3*5)+(2*2)+(1*0)=61
61 % 10 = 1
So 7005-20-1 is a valid CAS Registry Number.
7005-20-1Relevant academic research and scientific papers
Asymmetric Transformations of Proline and 2-Piperidinecarboxylic Acid via Formation of Salts with Optically Active Tartaric Acid
Shiraiwa, Tadashi,Shinjo, Kazuyuki,Kurokawa, Hidemoto
, p. 3251 - 3255 (2007/10/02)
The rates of racemization of optically active proline and 2-piperidinecarboxylic acid by using aldehydes as a catalyst tended to increase with a decrease in the acidity of the carboxylic acid used as solvent.Based on these results, the asymmetric transformations of DL-Pro and (RS)-Pia were carried out via formation of salts with (2R,3R)-tartaric acid to give optically pure L-Pro in over 80percent yield and (R)-Pia in 70percent yield.The asymmetric transformation of L-Pro was more successfully achieved by using (2S,3S)-tartaric acid to give optically pure D-Pro in 85percent yield based on the starting L-Pro.
