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2-(2-phenyl-3,4-dihydro-2H-chromen-4-yl)-1H-isoindole-1,3(2H)-dione is a complex organic compound with a molecular formula of C21H13NO3. It is a derivative of isoindole, which is a heterocyclic compound consisting of a benzene ring fused to a pyrrolidine ring. The molecule features a 2-phenyl-3,4-dihydro-2H-chromen-4-yl group attached to the isoindole core, which adds a phenyl ring and a dihydro-chromene moiety to the structure. 2-(2-phenyl-3,4-dihydro-2H-chromen-4-yl)-1H-isoindole-1,3(2H)-dione is known for its potential applications in the field of pharmaceuticals and materials science, particularly in the development of new drugs and advanced materials. Its unique structure and properties make it an interesting target for further research and development.

7154-63-4

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7154-63-4 Usage

Chromenyl group

A heterocyclic aromatic compound with a benzene ring and an oxygen atom.

Isoindole-1,3(2H)-dione group

A bicyclic compound with a fused indole ring and a carbonyl group.

Phenyl bridge

A benzene ring connecting the two main chemical groups.

Anti-inflammatory

The compound may help reduce inflammation in the body.

Antioxidant

The compound may help protect cells from damage caused by free radicals and oxidative stress.

Drug development

The compound's structural features make it a potential candidate for the development of new drugs.

Treatment of inflammation-related diseases

The compound's anti-inflammatory properties may be useful in treating conditions such as arthritis, asthma, and inflammatory bowel disease.

Treatment of oxidative stress-related diseases

The compound's antioxidant properties may be beneficial in treating conditions such as neurodegenerative diseases, cardiovascular diseases, and cancer.

Biological effects

More studies are needed to understand the compound's effects on living organisms and its potential therapeutic applications.

Potential applications

Further research is required to determine the compound's efficacy and safety in treating various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 7154-63-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7154-63:
(6*7)+(5*1)+(4*5)+(3*4)+(2*6)+(1*3)=94
94 % 10 = 4
So 7154-63-4 is a valid CAS Registry Number.

7154-63-4SDS

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-(2-phenyl-3,4-dihydro-2H-chromen-4-yl)isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 4-Phthalimidoflavan

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:7154-63-4 SDS

7154-63-4Downstream Products

7154-63-4Relevant academic research and scientific papers

STEREOSELECTIVITY AT BENZYLIC CARBON. FLAVANOIDS-V. SYNTHESIS OF TRANS-4-ACETAMIDOFLAVANS

Hirwe, A.,Marathe, K. G.,Mohorkar, S. S.,Ramdas, K.,Singh, C. B.

, p. 1539 - 1546 (2007/10/02)

Some reactions of 4-substituted flavans have been studied. 4-Chloro/bromo derivatives react under neutral conditions with phthalimide and acetonitrile leading to displacement of axial halogen by nitrogen with inversion.In contrast, irrespective of the ste

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