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2-(1-OXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)PROPANOIC ACID, a synthetic organic compound with the molecular formula C13H13NO3, is a member of the isoindoline derivatives class. 2-(1-OXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)PROPANOIC ACID features a propionic acid group attached to an isoindoline ring, which endows it with unique structural characteristics. Its potential pharmacological activities and applications in medicinal chemistry have attracted significant interest, making it a promising candidate for further research and development in drug discovery.

67266-14-2

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67266-14-2 Usage

Uses

Used in Pharmaceutical Industry:
2-(1-OXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)PROPANOIC ACID serves as a starting material for the synthesis of various drugs, leveraging its structural properties to contribute to the development of new therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(1-OXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)PROPANOIC ACID is utilized as a valuable building block for the production of diverse bioactive compounds. Its unique structure allows for the creation of a wide range of molecules with potential therapeutic applications.
Due to the lack of specific application reasons in the provided materials, the uses listed above are based on the general potential of the compound in the pharmaceutical and medicinal chemistry fields. Further research and development would be necessary to identify specific applications and reasons for the use of 2-(1-OXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)PROPANOIC ACID in various industries.

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

67266-14-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-oxo-1H-isoindol-2-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 2-(1-Oxo-1,3-dihydro-2H-isoindol-2-yl)propanoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67266-14-2 SDS

67266-14-2Downstream Products

67266-14-2Relevant academic research and scientific papers

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

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