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1-(2,4-DIFLUORO-PHENYL)-1H-PYRROLE-2-CARBALDEHYDE is a chemical compound with the molecular formula C11H7F2NO. It is a pyrrole derivative that contains a 2,4-difluoro-phenyl and a carbaldehyde group. 1-(2,4-DIFLUORO-PHENYL)-1H-PYRROLE-2-CARBALDEHYDE is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as its biological activities such as antimicrobial and anticancer properties. Furthermore, it has been evaluated for its use as a fluorescent probe for detecting metal ions, showcasing its versatility and value in both chemical and biological research.

125126-74-1

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125126-74-1 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
1-(2,4-DIFLUORO-PHENYL)-1H-PYRROLE-2-CARBALDEHYDE is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and functional groups make it a valuable component in the development of new drugs and pesticides, contributing to the advancement of these industries.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 1-(2,4-DIFLUORO-PHENYL)-1H-PYRROLE-2-CARBALDEHYDE has been studied for its potential as an antimicrobial agent. Its ability to inhibit the growth of harmful microorganisms makes it a promising candidate for the development of new antimicrobial treatments and products.
Used in Anticancer Applications:
1-(2,4-DIFLUORO-PHENYL)-1H-PYRROLE-2-CARBALDEHYDE has also been investigated for its potential anticancer properties. Its ability to target and disrupt cancer cell processes could lead to the development of new therapeutic strategies for the treatment of various types of cancer.
Used in Chemical Research:
As a fluorescent probe for detecting metal ions, 1-(2,4-DIFLUORO-PHENYL)-1H-PYRROLE-2-CARBALDEHYDE is used in chemical research to study and analyze the interactions between metal ions and other molecules. This application can provide valuable insights into the mechanisms of various chemical reactions and processes.
Used in Biological Research:
In the field of biological research, 1-(2,4-DIFLUORO-PHENYL)-1H-PYRROLE-2-CARBALDEHYDE is utilized for its potential in studying biological activities and interactions. Its fluorescent properties allow for the tracking and visualization of cellular processes, contributing to a better understanding of biological systems and mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 125126-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,2 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 125126-74:
(8*1)+(7*2)+(6*5)+(5*1)+(4*2)+(3*6)+(2*7)+(1*4)=101
101 % 10 = 1
So 125126-74-1 is a valid CAS Registry Number.

125126-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,4-difluorophenyl)pyrrole-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names -

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:125126-74-1 SDS

125126-74-1Downstream Products

125126-74-1Relevant articles and documents

Polycondensed heterocycles. VII. A convenient synthesis of pyrrolo[1,2-a]quinoxaline derivatives by intramolecular aromatic nucleophilic displacement

Campiani,Nacci,Corelli,Anzini

, p. 1567 - 1576 (2007/10/02)

4-(4-Methyl-1-piperazinyl)-7- trifluoromethylpyrrolo[1,2-a]quinoxaline (CGS 12066B) and related analogs were prepared in good overall yield through a reaction sequence involving as a key step in the intramolecular substitution of aromatic fluoride or nitr

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