132089-44-2 Usage
Uses
Used in Pharmaceutical Research:
2-(3-Methoxy-phenyl)-oxazole-4-carboxylic acid ethyl ester is used as a building block for the synthesis of pharmaceutical compounds due to its versatile chemical structure and potential to exhibit biological activities. It aids in the development of new drugs by providing a foundation for the creation of molecules with therapeutic properties.
Used in Organic Synthesis:
In the field of organic synthesis, 2-(3-Methoxy-phenyl)-oxazole-4-carboxylic acid ethyl ester is used as a key intermediate for the preparation of complex organic molecules. Its unique structure allows for various chemical reactions, facilitating the synthesis of a wide range of organic compounds for different applications.
Used in Medicinal Chemistry Research:
2-(3-Methoxy-phenyl)-oxazole-4-carboxylic acid ethyl ester is employed as a valuable tool in medicinal chemistry research. Its potential to exhibit various biological activities makes it suitable for the exploration of new therapeutic agents and the study of molecular interactions within biological systems.
Used in Bioactive Compounds Synthesis:
2-(3-METHOXY-PHENYL)-OXAZOLE-4-CARBOXYLIC ACID ETHYL ESTER is utilized in the synthesis of bioactive compounds, which are molecules that have an effect on biological systems. The ethyl ester derivative's structure allows for the development of compounds with potential applications in medicine, agriculture, and other industries where bioactive substances are required.
Check Digit Verification of cas no
The CAS Registry Mumber 132089-44-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,8 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132089-44:
(8*1)+(7*3)+(6*2)+(5*0)+(4*8)+(3*9)+(2*4)+(1*4)=112
112 % 10 = 2
So 132089-44-2 is a valid CAS Registry Number.
132089-44-2Relevant academic research and scientific papers
Design, synthesis and biological evaluation of 2,4-disubstituted oxazole derivatives as potential PDE4 inhibitors
Li, Ya-Sheng,Hu, De-Kun,Zhao, Dong-Sheng,Liu, Xing-Yu,Jin, Hong-Wei,Song, Gao-Peng,Cui, Zi-Ning,Zhang, Lian-Hui
, p. 1852 - 1859 (2017/03/08)
In this study, a series of pyrazole derivatives containing 4-phenyl-2-oxazole moiety were designed and synthesized in a concise way, some of which exhibited considerable inhibitory activity against PDE4B and blockade of LPS-induced TNF-α release. Compound
A silver-mediated one-step synthesis of oxazoles
Ritson, Dougal J.,Spiteri, Christian,Moses, John E.
supporting information; experimental part, p. 3519 - 3522 (2011/06/24)
A silver-mediated one-step procedure to 2,4-disubstituted and 2,4,5-trisubstituted oxazoles has been developed. The method is complementary to existing technologies, yet provides advantages with regard to simplicity, efficiency, and performance. The silver product can be readily recycled, thus minimizing waste.
Palladium-catalyzed direct arylations, alkenylations, and benzylations through C-H bond cleavages with sulfamates or phosphates as electrophiles
Ackermann, Lutz,Barfuesser, Sebastian,Pospech, Jola
supporting information; experimental part, p. 724 - 726 (2010/04/02)
(Figure Presented) catalytic system comprised of Pd(OAc)2 and bldentate ligand dppe enabled first direct arylatlons with moisture-stable aryl sulfamates as electrophlles, and proved applicable to unprecedented C-H bond functlonallzations with e
