637032-01-0 Usage
Description
(R)-2-(2,5-Dimethoxyphenyl)thiazolidine-4-carboxylic acid is a chemical compound characterized by a thiazolidine ring and a carboxylic acid group. It is a derivative of thiazolidine-4-carboxylic acid, featuring a phenyl group with two methoxy substituents. (R)-2-(2,5-Dimethoxyphenyl)thiazolidine-4-carboxylic acid has garnered attention for its potential pharmacological properties, which include anti-inflammatory and anti-tumor effects. Its unique structure and promising biological activities make it a subject of interest for researchers in the pharmaceutical and medicinal chemistry fields.
Uses
Used in Pharmaceutical Industry:
(R)-2-(2,5-Dimethoxyphenyl)thiazolidine-4-carboxylic acid is used as a potential therapeutic agent for various medical conditions due to its anti-inflammatory and anti-tumor effects. Its ability to modulate key biological pathways involved in inflammation and tumorigenesis positions it as a candidate for the development of new drugs to treat a range of diseases, including cancer and inflammatory disorders.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (R)-2-(2,5-Dimethoxyphenyl)thiazolidine-4-carboxylic acid serves as a valuable compound for further investigation and optimization. Researchers can explore its structure-activity relationships, synthesize analogs, and evaluate their potential as more effective and selective drug candidates. (R)-2-(2,5-Dimethoxyphenyl)thiazolidine-4-carboxylic acid's unique features may lead to the discovery of novel therapeutic agents with improved pharmacological profiles and reduced side effects.
Used in Drug Development:
(R)-2-(2,5-Dimethoxyphenyl)thiazolidine-4-carboxylic acid is utilized in the development of new drugs targeting specific medical conditions. Its pharmacological properties, such as anti-inflammatory and anti-tumor effects, make it a promising starting point for designing and synthesizing novel drug candidates. By optimizing its structure and functional groups, researchers can enhance its potency, selectivity, and pharmacokinetic properties, ultimately leading to more effective treatments for patients.
Check Digit Verification of cas no
The CAS Registry Mumber 637032-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,7,0,3 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 637032-01:
(8*6)+(7*3)+(6*7)+(5*0)+(4*3)+(3*2)+(2*0)+(1*1)=130
130 % 10 = 0
So 637032-01-0 is a valid CAS Registry Number.
637032-01-0Relevant articles and documents
Conformational analysis, spectral and catalytic properties of 1,3-thiazolidines, ligands for acetophenone hydrosilylation with diphenylsilane
Skvortsov,Uvarov,De Vekki,Studentsov,Skvortsov
scheme or table, p. 2007 - 2021 (2011/02/18)
2-Aryl- and 2-furyl-4-carboxy-1,3-thiazolidines were synthesized. Their spectral properties were studied, and conformational analysis was performed. It was shown that they exist in solution as an equilibrium of neutral and zwitter-ion forms. The influence
