96017-10-6 Usage
General Description
2-(1-Oxo-1,3-dihydro-2H-isoindol-2-yl)-3-phenylpropanoic acid is a complex organic compound that belongs to the class of chemicals known as isoindoles. Isoindoles are polycyclic compounds that contain an isoindole moiety, which is a bicyclic heterocycle made up of two benzene rings fused to a pyrrole ring. This specific chemical is characterized by a combination of isoindole structure and the presence of the phenylpropanoic acid group. The range of potential uses for compounds of this class is diverse, including pharmaceuticals, dyes, organic semiconductors, and photoinitiators for polymerization reactions. Characteristics of this compound, like stability, reactivity, and potential bioactivity, are highly dependent on its precise molecular structure, which needs to be considered in detail for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 96017-10-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,0,1 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 96017-10:
(7*9)+(6*6)+(5*0)+(4*1)+(3*7)+(2*1)+(1*0)=126
126 % 10 = 6
So 96017-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H15NO3/c19-16-14-9-5-4-8-13(14)11-18(16)15(17(20)21)10-12-6-2-1-3-7-12/h1-9,15H,10-11H2,(H,20,21)/p-1/t15-/m1/s1
96017-10-6Relevant articles and documents
Imides
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, (2008/06/13)
Cyclic imides are inhibitors of tumor necrosis factor α and can be used to combat cachexia, endotoxic shock, and retrovirus replication. A typical embodiment is 2-(2,6-dioxo-3-piperidinyl)-4-azaisoindoline-1,3-dione.
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
Synthesis of the 5H-Pyrroloisoindole Ring with 1,3-Dipolar Cycloaddition Reactions
New, J. S.,Yevich, J. P.
, p. 1355 - 1360 (2007/10/02)
The 1,3-dipolar cycloaddition reaction between mesoionic oxazolines, formed from either 1,3-dihydro-2-substituted-2H-isoindole-1-carboxylic acids or 1,3-dihydro-1-oxo-α-substituted-2H-isoindole-2-acetic acids, and dimethylacetylene dicarboxylate has led t
