153180-21-3 Usage
Uses
Used in Pharmaceutical Industry:
4-Oxazolecarboxylic acid, 2-(1-methylethyl)-(9CI) is used as a potential pharmaceutical compound for its possible antimicrobial, anticancer, and antiviral properties. Its unique structure and oxazole ring may contribute to its biological activities, making it a candidate for further research and development in drug discovery.
Used in Drug Discovery and Development:
In the Drug Discovery and Development industry, 4-Oxazolecarboxylic acid, 2-(1-methylethyl)-(9CI) is used as a starting material or intermediate in the synthesis of various pharmaceutical agents. Its unique chemical structure and potential biological activities make it a valuable compound for exploring new therapeutic agents and treatments.
Used in Research and Development:
4-Oxazolecarboxylic acid, 2-(1-methylethyl)-(9CI) is used as a research compound in academic and industrial laboratories. It serves as a valuable tool for studying the structure-activity relationships of oxazole derivatives and their potential applications in various fields, including medicinal chemistry, materials science, and environmental chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 153180-21-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,8 and 0 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 153180-21:
(8*1)+(7*5)+(6*3)+(5*1)+(4*8)+(3*0)+(2*2)+(1*1)=103
103 % 10 = 3
So 153180-21-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO3/c1-4(2)6-8-5(3-11-6)7(9)10/h4-5H,3H2,1-2H3,(H,9,10)
153180-21-3Relevant academic research and scientific papers
Widely Exploited, Yet Unreported: Regiocontrolled Synthesis and the Suzuki–Miyaura Reactions of Bromooxazole Building Blocks
Solomin, Vitalii V.,Radchenko, Dmytro S.,Slobodyanyuk, Evgeniy Y.,Geraschenko, Oleksandr V.,Vashchenko, Bohdan V.,Grygorenko, Oleksandr O.
, p. 2884 - 2898 (2019/03/07)
An approach to synthesis of 2-, 4-, and 5-bromooxazoles is described. The method was optimized, and its scope was extended to all three isomeric parents, as well as various alkyl- and aryl-substituted bromooxazoles. It was found that direct regiocontrolled lithiation followed by reaction with electrophilic bromine source was common for all substrates and led exclusively to the target substituted 2-, 4- and 5-bromooxazoles on multigram scale. The utility of the multipurpose building blocks obtained in this work was demonstrated in the Suzuki–Miyaura cross-coupling reaction under parallel synthesis conditions.
Dimethyl Aminomalonate: A Useful C-3 Unit in a Mild, Direct Synthesis of Oxazole-4-carboxylates
Shapiro, Rafael
, p. 5759 - 5764 (2007/10/02)
N-Acyl derivatives of the title compound undergo oxidative cyclization upon treatment with N-chlorosuccinimide in DMF to form dimethyl 4,5-dihydro-5-(phenylthio)oxazole-4,4-dicarboxylates 4 which then are decarbomethoxylated with concomitant loss of thiop
