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1H-Isoindole, 2,3-dihydro-2-(2-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109514-64-9

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109514-64-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109514-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,1 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109514-64:
(8*1)+(7*0)+(6*9)+(5*5)+(4*1)+(3*4)+(2*6)+(1*4)=119
119 % 10 = 9
So 109514-64-9 is a valid CAS Registry Number.

109514-64-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-methoxyphenyl)-1,3-dihydroisoindole

1.2 Other means of identification

Product number -
Other names HMS1382G19

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:109514-64-9 SDS

109514-64-9Relevant academic research and scientific papers

Visible-light induced isoindoles formation to trigger intermolecular diels-alder reactions in the presence of air

Lin, Chao,Zhen, Le,Cheng, Yong,Du, Hong-Jin,Zhao, Hui,Wen, Xiaoan,Kong, Ling-Yi,Xu, Qing-Long,Sun, Hongbin

supporting information, p. 2684 - 2687 (2015/06/16)

Visible-light induced isoindole formation triggered an intermolecular Diels-Alder reaction with dienophiles such as acetylenedicarboxylate and maleimides in the presence of air. The reaction resulted in excellent diastereoselctivity and high yields under

An efficient method for the synthesis of 2, 3-dihydro-lH-isoindoles

Subbarayappa, Adimurthy,Patoliya, Paresh U.

experimental part, p. 545 - 552 (2009/12/06)

The synthesis of Af-substituted 2, 3-dihydro-lH-isoindoles from α, α'-dibromo-o-xylene and various primary amines in basic medium under ambient conditions is described. Especially the selection of 1, 4-dioxane as solvent and sodium hydroxide as suitable base to maintain the homogeneity of the medium are key steps to promote the reaction efficiently. Primary alkyl amines react faster as compared to their aromatic analogues under the conditions studied. Irrespective of the starting amine used, all the reactions proceed smoothly and provide 2, 3-dihydro-lH-isoindoles derivatives in excellent yields compared to hitherto known methods.

CHARGE-TRANSFER COMPLEXES OF ISOINDOLINES WITH 1,4-BENZOQUINONES

Mourad, Aboul-fetouh E.,Nour-el-din, Ahmed M.,Hassan, Alaa A.,Doepp, Dietrich

, p. 1045 - 1052 (2007/10/02)

Charge-transfer (CT) complexes of various N-arylisoindolines as donors with 1,4-benzoquinones as ?-acceptors have been studied spectrophotometrically.Effects of substituents

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