158476-38-1 Usage
Class
Thiazolidine carboxylic acids
It belongs to a group of organic compounds containing a thiazolidine ring and a carboxylic acid group.
Molecular weight
235.29 g/mol
The mass of one mole of 2-(3-methoxy-phenyl)-thiazolidine-4-carboxylic acid is 235.29 grams.
Thiazolidine ring
A five-membered heterocyclic ring
The compound contains a thiazolidine ring, which is a five-membered ring with three carbon atoms and two heteroatoms (one sulfur and one nitrogen).
Carboxylic acid group
-COOH
The compound has a carboxylic acid group, which is a functional group consisting of a carbonyl group (C=O) and a hydroxyl group (-OH) bonded to the same carbon atom.
3-Methoxy-phenyl substituent
-OCH3 attached to a phenyl ring
The compound has a 3-methoxy-phenyl group, which is a phenyl ring with a methoxy group (-OCH3) attached to the third carbon atom.
Pharmaceutical research and drug development
Potential biological activities
2-(3-Methoxy-phenyl)-thiazolidine-4-carboxylic acid can be used in pharmaceutical research and drug development due to its potential biological activities.
Medicinal chemistry and pharmacology
Interesting for further studies
The presence of the 3-methoxy-phenyl substituent may impart specific properties and activities to the compound, making it interesting for further studies in medicinal chemistry and pharmacology.
Check Digit Verification of cas no
The CAS Registry Mumber 158476-38-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,4,7 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 158476-38:
(8*1)+(7*5)+(6*8)+(5*4)+(4*7)+(3*6)+(2*3)+(1*8)=171
171 % 10 = 1
So 158476-38-1 is a valid CAS Registry Number.
158476-38-1Relevant articles and documents
Synthesis, in vitro structure-activity relationship, and in vivo studies of 2-arylthiazolidine-4-carboxylic acid amides as anticancer agents
Lu, Yan,Wang, Zhao,Li, Chien-Ming,Chen, Jianjun,Dalton, James T.,Li, Wei,Miller, Duane D.
experimental part, p. 477 - 495 (2010/04/29)
A series of (2RS,4R)-2-arylthiazolidine-4-carboxylic acid amide (ATCAA) was synthesized. Antiproliferative activity against melanoma and prostate cancer cells compared with control cells (fibroblast and RH7777, respectively) was evaluated. Compound 3id sh
Heterocyclic Compounds from Sugars, XV: On the Configuration of Chiral C-2 Substituted 1,3-Thiazolidine-4-carboxylic Acids. Chirality Transfer to C-3 of 3,4-Dihydro-1H-pyrrolothiazoles
Gyoergydeak, Z.,Szilagyi, L.,Kajtar, J.,Argay, G.,Kalman, A.
, p. 189 - 208 (2007/10/02)
5-Substituted 3,4-dihydro-pyrrolothiazole-6,7-dicarboxylic acid esters 3 are obtained from 2-substituted-3-acyl-1,3-thiazolidine-4-carboxylic acids, 1 in -cycloaddition reactions via mesoionic oxazolone ("muenchnone") intermediates.The chirali
