14347-75-2 Usage
Uses
Used in Pharmaceutical Industry:
(2RS,4R)-2-isopropylthiazolidine-4-carboxylic acid is utilized as a pharmaceutical agent for the treatment of diabetes and metabolic disorders. Its insulin-sensitizing and anti-inflammatory properties make it a promising candidate for developing new drugs to manage these conditions more effectively.
Used in Neuroprotective Applications:
In the field of neuroprotection, (2RS,4R)-2-isopropylthiazolidine-4-carboxylic acid serves as a neuroprotective agent due to its antioxidant properties. This makes it a potential therapeutic option for conditions where oxidative stress plays a significant role in neuronal damage.
Used in Antioxidant Formulations:
(2RS,4R)-2-isopropylthiazolidine-4-carboxylic acid is used as an antioxidant in various formulations, capitalizing on its ability to combat oxidative stress. This application is relevant across multiple industries, including pharmaceuticals, cosmetics, and food and beverage, where antioxidants are crucial for maintaining product integrity and health benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 14347-75-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,4 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14347-75:
(7*1)+(6*4)+(5*3)+(4*4)+(3*7)+(2*7)+(1*5)=102
102 % 10 = 2
So 14347-75-2 is a valid CAS Registry Number.
14347-75-2Relevant academic research and scientific papers
Asymmetric synthesis of 2-alkyl-3-thiazoline carboxylates: Stereochemistry of the MnO2-mediated oxidation of cis- and trans-2-alkyl-thiazolidine-(4R)-carboxylates
Fernandez, Xavier,Duach, Elisabet
, p. 1279 - 1286 (2007/10/03)
The asymmetric synthesis of a series of 3-thiazoline carboxylates, 2, was effected by MnO2 oxidation of the corresponding cis/trans thiazolidines, 1. The stereochemistry of the oxidation reaction was studied using NMR and chiral GC analyses. Compounds 2 were obtained with enantiomeric excesses (e.e.s) in the range of 40-100%.
