118721-55-4 Usage
General Description
2-(3-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid is a chemical compound with a thiazolidine ring and a carboxylic acid group. It is also known as CBZ-thiazolidine-4-carboxylic acid and is commonly used in the synthesis of pharmaceuticals and agrochemicals. 2-(3-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid has been shown to exhibit anti-inflammatory and antibacterial properties, making it a potential candidate for drug development. Its thiazolidine ring structure is of interest due to its ability to form stable complexes with metal ions, which could be useful in various industrial applications. Overall, this chemical has diverse potential uses and has generated interest in the fields of medicinal chemistry and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 118721-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,7,2 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118721-55:
(8*1)+(7*1)+(6*8)+(5*7)+(4*2)+(3*1)+(2*5)+(1*5)=124
124 % 10 = 4
So 118721-55-4 is a valid CAS Registry Number.
118721-55-4Relevant articles and documents
An Experimental Toolbox for Structure-Based Hit Discovery for P. aeruginosa FabF, a Promising Target for Antibiotics
Espeland, Ludvik Olai,Georgiou, Charis,Klein, Raphael,Bhukya, Hemalatha,Haug, Bengt Erik,Underhaug, Jarl,Mainkar, Prathama S.,Brenk, Ruth
, p. 2715 - 2726 (2021)
FabF (3-oxoacyl-[acyl-carrier-protein] synthase 2), which catalyses the rate limiting condensation reaction in the fatty acid synthesis II pathway, is an attractive target for new antibiotics. Here, we focus on FabF from P. aeruginosa (PaFabF) as antibiot
Synthesis, characterization and antibacterial activities of N-tert-butoxycarbonyl-thiazolidine carboxylic acid
Song, Zhong-Cheng,Ma, Gao-Yuan,Zhu, Hai-Liang
, p. 24824 - 24833 (2015/03/30)
A possible mechanism of dynamic kinetic resolution by the formation of N-tert-butoxycarbonyl-thiazolidine carboxylic acid was proposed and validated by a quantitative density functional theoretical calculation according to Curtin-Hammett principle. Such a
