67266-14-2 Usage
General Description
2-(1-oxo-1,3-dihydro-2H-isoindol-2-yl)propanoic acid is a chemical compound that belongs to the class of isoindoline derivatives. It is a synthetic organic compound with molecular formula C13H13NO3. 2-(1-OXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)PROPANOIC ACID is used in the pharmaceutical industry as a starting material for the synthesis of various drugs and also has potential applications in the field of medicinal chemistry. Its structure contains a propionic acid moiety attached to an isoindoline ring, making it a valuable building block for the production of diverse bioactive compounds. Due to its structural characteristics, 2-(1-oxo-1,3-dihydro-2H-isoindol-2-yl)propanoic acid has garnered attention for its potential pharmacological activities and may be of interest for further research and development in drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 67266-14-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,2,6 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67266-14:
(7*6)+(6*7)+(5*2)+(4*6)+(3*6)+(2*1)+(1*4)=142
142 % 10 = 2
So 67266-14-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO3/c1-7(11(14)15)12-6-8-4-2-3-5-9(8)10(12)13/h2-5,7H,6H2,1H3,(H,14,15)/p-1/t7-/m1/s1
67266-14-2Relevant articles and documents
A Simple One-step Synthesis of N-Substituted Isoindolin-1-ones. Diastereofacially Selective Protonation of an Intermediate Isoindolinol
Grigg, Ronald,Gunaratne, H. Q. Nimal,Sridharan, Visuvanathar
, p. 1183 - 1184 (2007/10/02)
α-Amino acids and their methyl esters, arylamines, heterocyclic amines and, less efficiently, aryl substituted aliphatic amines, react with o-phthaldialdehyde in the presence of acetic acid to give N-substituted isoindolin-1-ones in excellent yield; deute
New acylated derivatives of 2(4 aminophenyl)propionic acid as potential antiinflammatory agents
Rufer,Bahlmann,Kapp
, p. 193 - 198 (2007/10/06)
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