20839-78-5 Usage
Uses
Used in Pharmaceutical Industry:
(4-METHOXY-BENZYLAMINO)-ACETIC ACID is used as a pharmaceutical intermediate for its ability to modify the pharmacokinetic properties of drugs. This modification can enhance drug absorption, distribution, metabolism, and excretion, thereby potentially improving the efficacy and safety of medications.
Used in Organic Synthesis:
In the field of organic chemistry, (4-METHOXY-BENZYLAMINO)-ACETIC ACID is used as a building block for the synthesis of various organic compounds. Its unique structure, which includes a benzene ring and a methoxy group, allows it to participate in a range of chemical reactions, facilitating the creation of new molecules with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 20839-78-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,3 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20839-78:
(7*2)+(6*0)+(5*8)+(4*3)+(3*9)+(2*7)+(1*8)=115
115 % 10 = 5
So 20839-78-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3/c1-14-9-4-2-8(3-5-9)6-11-7-10(12)13/h2-5,11H,6-7H2,1H3,(H,12,13)
20839-78-5Relevant academic research and scientific papers
Vibrational Spectroscopic Characterization and DFT Study of Palladium(II) Complexes with N-Benzyliminodiacetic Acid Derivatives
Smre?ki, Neven,Ron?evi?, Igor,Popovi?, Zora
, p. 1285 - 1291 (2016/11/25)
The reactions of N-benzyliminodiacetic acid (BnidaH2) and its para-substituted derivatives, namely N-(p-chlorobenzyl)iminodiacetic acid (p-ClBnidaH2), N-(p-nitrobenzyl)iminodiacetic acid (p-NO2BnidaH2), and N-(p
An intramolecular azomethine ylide-alkene cycloaddition approach to pyrrolo[3,2-c]quinolines-synthesis of a C2-truncated martinelline model
Mahmud, Hossen,Lovely, Carl J,Rasika Dias
, p. 4095 - 4105 (2007/10/03)
The hexahydropyrrolo[3,2-c]quinoline core found in the Martinella alkaloids was constructed through an intramolecular [3+2] azomethine ylide-alkene cycloaddition. Some chemical manipulations of the tricycle are reported.
