55040-86-3 Usage
Uses
Used in Medicinal Chemistry:
2-Morpholin-4-yl-4-phenyl-thiazole-5-carboxylic acid ethyl ester is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a versatile building block in the development of new drugs with potential therapeutic applications.
Used in Drug Development:
In the pharmaceutical industry, 2-Morpholin-4-yl-4-phenyl-thiazole-5-carboxylic acid ethyl ester is used as a lead compound for the discovery of novel therapeutic agents. Its pharmacological properties and potential biological activity make it a promising candidate for further research and development into new medications.
Used in Biological Research:
2-Morpholin-4-yl-4-phenyl-thiazole-5-carboxylic acid ethyl ester is utilized in biological research as a tool compound to study the interactions between molecules and biological targets. Its unique structure allows researchers to investigate its binding affinity, selectivity, and potential effects on various biological pathways.
Used in Chemical Synthesis:
2-Morpholin-4-yl-4-phenyl-thiazole-5-carboxylic acid ethyl ester is employed as a reagent in various chemical synthesis processes. Its functional groups, such as the ester and carboxylic acid, enable it to participate in a range of chemical reactions, making it a valuable component in the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 55040-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,0,4 and 0 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 55040-86:
(7*5)+(6*5)+(5*0)+(4*4)+(3*0)+(2*8)+(1*6)=103
103 % 10 = 3
So 55040-86-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H18N2O3S/c1-2-21-15(19)14-13(12-6-4-3-5-7-12)17-16(22-14)18-8-10-20-11-9-18/h3-7H,2,8-11H2,1H3
55040-86-3Relevant academic research and scientific papers
Synthesis and exploration of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives for their effects against carbonic anhydrase I, II, IX and XII isoforms as a non-sulfonamide class of inhibitors
Swain, Baijayantimala,Singh Digwal, Chander,Angeli, Andrea,Alvala, Mallika,Singh, Priti,Supuran, Claudiu T.,Arifuddin, Mohammed
, (2019/09/12)
Novel series of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives (8a–s) have been synthesized and explored as a non-sulfonamide class of carbonic anhydrase (CA, EC 4.2.1.1) inhibitors. The newly synthesized molecules were evaluated for their CA in
One-pot chemoenzymatic multicomponent synthesis of thiazole derivatives
Zheng, Hui,Mei, Yi-Jia,Du, Kui,Cao, Xian-Ting,Zhang, Peng-Fei
, p. 13425 - 13433 (2014/01/06)
A novel chemoenzymatic one-pot multicomponent synthesis of thiazole derivatives was developed. A series of thiazole derivatives were synthesized with high yields up to 94% under mild enzyme-catalyzed conditions. The blank and control experiments reveal that trypsin from porcine pancreas (PPT) displayed great catalytic activity to promote this reaction and showed a wide tolerance range towards different substrate amines. This trypsin-catalyzed multicomponent conversion method provides a novel strategy to synthesize thiazole derivatives and expands the application of enzymes in organic synthesis.
