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1971-50-2

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1971-50-2 Usage

Structure

A derivative of isoindole with a lactone (cyclic ester) group, an acetyl group, and a hydroxy group

Type

A chemical compound

Usage

Commonly used in organic synthesis

Applications

Potential applications in pharmaceuticals and as an intermediate in the synthesis of other organic compounds

Importance

Valuable for research and development in various industries due to its biological and chemical properties

Check Digit Verification of cas no

The CAS Registry Mumber 1971-50-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,7 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1971-50:
(6*1)+(5*9)+(4*7)+(3*1)+(2*5)+(1*0)=92
92 % 10 = 2
So 1971-50-2 is a valid CAS Registry Number.

1971-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetyl-3-hydroxy-3H-isoindol-1-one

1.2 Other means of identification

Product number -
Other names 2-Acetyl-3-hydroxy-dihydro-isoindol-1-on

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:1971-50-2 SDS

1971-50-2Downstream Products

1971-50-2Relevant articles and documents

Cu/Fe Catalyzed Intermolecular Oxidative Amination of Benzylic C-H Bonds

Liu, Cong,Zhang, Qi,Li, Hongbo,Guo, Shuangxi,Xiao, Bin,Deng, Wei,Liu, Lei,He, Wei

, p. 6208 - 6212 (2016)

We report a Cu/Fe co-catalyzed Ritter-type C-H activation/amination reaction that allows efficient and selective intermolecular functionalization of benzylic C-H bonds. This new reaction is featured by simple reaction conditions, readily available reagents and general substrate scope, allowing facile synthesis of biologically interesting nitrogen containing heterocycles. The Cu and Fe salts were found to play distinct roles in this cooperative catalysis. With a little help: A Ritter-type intermolecular amination of benzylic C-H bonds with acetonitrile, co-catalyzed by CuII/FeIII is reported. A wide array of biologically interesting nitrogen containing heterocycles was prepared from 2-alkyl benzoic acids and heteroaromatic carboxylic acids under operationally simple conditions. The Cu and Fe salts were found to play distinct roles in this cooperative catalysis.

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