59256-45-0 Usage
Uses
Used in Pharmaceutical Synthesis:
4-(4-Ethoxyanilino)-4-oxobutanoic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of drugs with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Chemical Research:
As a reagent in chemical research, 4-(4-Ethoxyanilino)-4-oxobutanoic acid aids in the investigation of chemical reactions and processes. Its properties make it a useful tool for understanding the behavior of organic compounds and their interactions with other molecules.
Used in Drug Development:
4-(4-ETHOXYANILINO)-4-OXOBUTANOIC ACID's chemical structure and properties make it suitable for the development of new drugs and bioactive compounds. Its potential applications in medicine highlight its importance in the discovery and creation of novel therapeutic agents.
Used in Laboratory Settings:
Due to its potential health hazards, 4-(4-Ethoxyanilino)-4-oxobutanoic acid should only be handled by trained professionals in appropriate laboratory settings. Its use in these controlled environments ensures the safety of researchers and the integrity of experimental outcomes.
Check Digit Verification of cas no
The CAS Registry Mumber 59256-45-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,5 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59256-45:
(7*5)+(6*9)+(5*2)+(4*5)+(3*6)+(2*4)+(1*5)=150
150 % 10 = 0
So 59256-45-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO4/c1-2-17-10-5-3-9(4-6-10)13-11(14)7-8-12(15)16/h3-6H,2,7-8H2,1H3,(H,13,14)(H,15,16)
59256-45-0Relevant academic research and scientific papers
Solid-phase synthesis of N-aryl succinimides
Rad-Moghadam, Kurosh,Kheyrkhah, Leila
experimental part, p. 2108 - 2115 (2009/10/17)
A new method upon adopting a solid-phase strategy for synthesis of N-aryl succinimides is described here, using the silica-bound benzoyl chloride (SBBC) as dehydrating agent in reaction with N-arylsuccinamic acids. The main advantage of this method is the
