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2-(furan-2-yl)-1H-isoindole-1,3(2H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30739-23-2

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30739-23-2 Usage

Heterocyclic compound

furan ring and isoindole-dione ring
2-(furan-2-yl)-1H-isoindole-1,3(2H)-dione is a heterocyclic compound, meaning it contains a ring structure with both carbon and hetero atoms (such as oxygen or nitrogen). In this case, it has a furan ring (a five-membered ring with one oxygen atom) and an isoindole-dione ring (a six-membered ring with a nitrogen atom and two carbonyl groups).

Building block for synthesis

complex organic molecules
2-(furan-2-yl)-1H-isoindole-1,3(2H)-dione is often used in chemical research as a building block for the synthesis of more complex organic molecules. This means that it can be used as a starting material to create a variety of other organic compounds with different properties and applications.

Potential anti-inflammatory agent

pharmaceutical applications
The compound has shown potential as an anti-inflammatory agent, which means it may be useful in the development of medications to reduce inflammation in the body. This could lead to new pharmaceutical applications for the treatment of various inflammatory conditions.

Production of dyes and pigments

characteristic color and structure
Due to its unique chemical structure and characteristic color, 2-(furan-2-yl)-1H-isoindole-1,3(2H)-dione has been used in the production of dyes and pigments. This makes it a valuable compound for industries that rely on coloring materials, such as textiles, paints, and plastics.

Organic electronics and optoelectronics

potential applications
The compound has also been investigated for its potential use in organic electronics and optoelectronic devices. This means that it may have properties that make it suitable for use in devices that convert light into electricity or modulate the flow of light, such as organic light-emitting diodes (OLEDs) or organic solar cells.

Check Digit Verification of cas no

The CAS Registry Mumber 30739-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,3 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30739-23:
(7*3)+(6*0)+(5*7)+(4*3)+(3*9)+(2*2)+(1*3)=102
102 % 10 = 2
So 30739-23-2 is a valid CAS Registry Number.

30739-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(furan-2-yl)isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names N-furan-2-yl-phthalimide

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:30739-23-2 SDS

30739-23-2Downstream Products

30739-23-2Relevant academic research and scientific papers

N -aminopyridinium salts as precursors for N-centered radicals - Direct amidation of arenes and heteroarenes

Greulich, Tobias W.,Daniliuc, Constantin G.,Studer, Armido

supporting information, p. 254 - 257 (2015/03/05)

Readily prepared N-aminopyridinium salts are valuable precursors for the generation of N-centered radicals. Reduction of these salts by single electron transfer allows for clean generation of amidyl radicals. It is shown that direct radical C-H amination of heteroarenes and arenes can be achieved with N-aminopyridinium salts under mild conditions by using photoredox catalysis.

N-acyloxyphthalimides as nitrogen radical precursors in the visible light photocatalyzed room temperature C-H amination of arenes and heteroarenes

Allen, Laura J.,Cabrera, Pablo J.,Lee, Melissa,Sanford, Melanie S.

supporting information, p. 5607 - 5610 (2014/05/06)

This paper reports a room temperature visible light photocatalyzed method for the C-H amination of arenes and heteroarenes. A key enabling advance in this work is the design of N-acyloxyphthalimides as precursors to nitrogen-based radical intermediates for these transformations. A broad substrate scope is presented, including the selective meta-amination of pyridine derivatives. A radical aromatic substitution mechanism is proposed.

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