16141-44-9 Usage
Uses
Used in Pharmaceutical Industry:
4-(3-Methoxyanilino)-4-oxobutanoic acid is used as a pharmaceutical compound for its potential therapeutic effects. Its unique chemical structure allows it to interact with biological targets, making it a promising candidate for the development of new drugs.
Used in Research Applications:
4-(3-Methoxyanilino)-4-oxobutanoic acid is used as a research tool to study its structural and functional properties. Its unique chemical structure provides opportunities for further investigation into its potential applications in drug development and medical research.
Check Digit Verification of cas no
The CAS Registry Mumber 16141-44-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,4 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16141-44:
(7*1)+(6*6)+(5*1)+(4*4)+(3*1)+(2*4)+(1*4)=79
79 % 10 = 9
So 16141-44-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H13NO4/c1-16-9-4-2-3-8(7-9)12-10(13)5-6-11(14)15/h2-4,7H,5-6H2,1H3,(H,12,13)(H,14,15)
16141-44-9Relevant academic research and scientific papers
Synthesis of 3-(5-amino-1: H -1,2,4-triazol-3-yl)propanamides and their tautomerism
Lim, Felicia Phei Lin,Tan, Lin Yuing,Tiekink, Edward R. T.,Dolzhenko, Anton V.
, p. 22351 - 22360 (2018/07/03)
Two complementary pathways for the preparation of N-substituted 3-(5-amino-1H-1,2,4-triazol-3-yl)propanamides (5) were proposed and successfully realized in the synthesis of 20 representative examples. These methods use the same types of starting material
Substituent chemical shifts of N-arylsuccinanilic acids, N-arylsuccinimides, N-arylmaleanilic acids, and N-arylmaleimides
Lee, Hye Sun,Yu, Ji Sook,Lee, Chang Kiu
scheme or table, p. 711 - 715 (2010/07/05)
NMR spectra of a series of N-arylsuccinanilic acids, N-arylsuccinimides, N-arylmaleanilic acids, and N-arylmaleimides were examined to estimate the electronic effect of the amide and imide groups on the chemical shifts of the hydrogen and carbon nuclei of the benzene ring.
