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1-(2,4-DIMETHYL-PHENYL)-PYRROLE-2,5-DIONE is a pyrrole-2,5-dione derivative with a molecular formula of C12H11NO2. It features a 2,4-dimethylphenyl substituent, which contributes to its unique chemical and biological properties. 1-(2,4-DIMETHYL-PHENYL)-PYRROLE-2,5-DIONE is of interest in the fields of organic synthesis and pharmaceutical research due to its potential biological activities and pharmacological properties.

1080-52-0

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1080-52-0 Usage

Uses

Used in Pharmaceutical Research:
1-(2,4-DIMETHYL-PHENYL)-PYRROLE-2,5-DIONE is used as a research compound for its potential anti-cancer properties. It has been studied for its ability to target and inhibit specific cancer-related pathways, making it a promising candidate for the development of new cancer therapies.
1-(2,4-DIMETHYL-PHENYL)-PYRROLE-2,5-DIONE is also used as an anti-inflammatory agent. Its potential to modulate inflammatory responses could lead to the development of new treatments for various inflammatory conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2,4-DIMETHYL-PHENYL)-PYRROLE-2,5-DIONE serves as a key intermediate or building block for the synthesis of more complex organic molecules. Its unique structure allows for further functionalization and modification, enabling the creation of novel compounds with diverse applications.
Used in Protein-Protein Interaction Inhibition:
1-(2,4-DIMETHYL-PHENYL)-PYRROLE-2,5-DIONE is used as a potential inhibitor of protein-protein interactions. Its ability to disrupt specific protein interactions could have implications in the development of targeted therapies for various diseases, including cancer and inflammatory disorders.
Overall, 1-(2,4-DIMETHYL-PHENYL)-PYRROLE-2,5-DIONE is a versatile chemical compound with a wide range of potential applications in pharmaceutical research, organic synthesis, and the development of novel therapeutic agents. Its unique structure and promising biological activities make it an interesting target for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 1080-52-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1080-52:
(6*1)+(5*0)+(4*8)+(3*0)+(2*5)+(1*2)=50
50 % 10 = 0
So 1080-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO2/c1-8-3-4-10(9(2)7-8)13-11(14)5-6-12(13)15/h3-7H,1-2H3

1080-52-0SDS

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 1-(2,4-dimethylphenyl)pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names 2,4-Dimethylphenylmaleimide

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 -
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More Details:1080-52-0 SDS

1080-52-0Relevant academic research and scientific papers

Aerobic Oxidative EDA Catalysis: Synthesis of Tetrahydroquinolines Using an Organocatalytic EDA Active Acceptor

Runemark, August,Sundén, Henrik

, p. 1457 - 1469 (2022/02/07)

A catalytic electron donor-acceptor (EDA) complex for the visible-light-driven annulation reaction between activated alkenes and N,N-substituted dialkyl anilines is reported. The key photoactive complex is formed in situ between dialkylated anilines as do

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