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Imidazo[1,2-a]pyridine-2-carboxamide (9CI) is a tricyclic chemical compound with a unique fused structure, widely recognized in the pharmaceutical industry as a key building block for the synthesis of biologically active molecules. Characterized by its antiviral, antifungal, antibacterial, and anticancer properties, Imidazo[1,2-a]pyridine-2-carboxamide (9CI) also exhibits the capacity to inhibit specific enzymes and receptors, positioning it as a promising candidate for drug development. Its diverse pharmacological activities and structural attributes render Imidazo[1,2-a]pyridine-2-carboxamide (9CI) a significant entity in medicinal chemistry and drug discovery endeavors.

39031-44-2

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39031-44-2 Usage

Uses

Used in Pharmaceutical Industry:
Imidazo[1,2-a]pyridine-2-carboxamide (9CI) serves as a crucial building block for the synthesis of biologically active compounds, leveraging its diverse pharmacological properties to contribute to the development of new drugs.
Used in Antiviral Applications:
Within the realm of antiviral drug development, Imidazo[1,2-a]pyridine-2-carboxamide (9CI) is utilized for its ability to combat viral infections, potentially leading to the creation of novel antiviral medications.
Used in Antifungal Applications:
In the context of antifungal treatments, Imidazo[1,2-a]pyridine-2-carboxamide (9CI) is applied to develop compounds that target and inhibit fungal growth, offering a new avenue for treating fungal infections.
Used in Antibacterial Applications:
Imidazo[1,2-a]pyridine-2-carboxamide (9CI) is employed in the development of antibacterial agents, capitalizing on its capacity to inhibit bacterial activity and contributing to the fight against antibiotic-resistant strains.
Used in Anticancer Applications:
Imidazo[1,2-a]pyridine-2-carboxamide (9CI) is harnessed in oncology research and drug development, where its anticancer properties are explored for potential use in treating various types of cancer.
Used in Enzyme and Receptor Inhibition:
Imidazo[1,2-a]pyridine-2-carboxamide (9CI) is utilized in the modulation of enzyme and receptor activities, providing a means to interfere with disease-causing biological processes and offering therapeutic benefits in multiple medical conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 39031-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,3 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39031-44:
(7*3)+(6*9)+(5*0)+(4*3)+(3*1)+(2*4)+(1*4)=102
102 % 10 = 2
So 39031-44-2 is a valid CAS Registry Number.

39031-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name imidazo[1,2-a]pyridine-2-carboxamide

1.2 Other means of identification

Product number -
Other names 2-Carbamoylimidazo<1,2-a>pyridin

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:39031-44-2 SDS

39031-44-2Relevant academic research and scientific papers

Bioinspired imidazo[1,2-a:4,5-c’]dipyridines with dual antiproliferative and anti-migrative properties in human cancer cells: The SAR investigation

Alzain, Abdulrahim A.,Brisson, Lucie,Delaye, Pierre-Olivier,Pénichon, Mélanie,Chadet, Stéphanie,Besson, Pierre,Chevalier, Stéphan,Allouchi, Hassan,Mohamed, Magdi A.,Roger, Sébastien,Enguehard-Gueiffier, Cécile

, (2021/04/09)

Herein, we report the design, synthesis and evaluation of novel bioinspired imidazo[1,2-a:4,5c’]dipyridines. The structural optimization identified four anti-proliferative compounds. Compounds 11, 18, 19 and 20 exhibited excellent anticancer activities in

Grignard reagent-promoted 6-endo-dig cyclization: Instantaneous synthesis of original dipyrido[1,2-a:3′,4′-d]imidazole

Oudot, Romain,Costes, Philippe,Allouchi, Hassan,Pouvreau, Mélanie,Abarbri, Mohamed,Gueiffier, Alain,Enguehard-Gueiffier, Cécile

scheme or table, p. 9576 - 9581 (2011/12/14)

Dipyrido[1,2-a:3′,4′-d]imidazole derivatives can be readily synthetized from various 3-alkyne-2-cyanoimidazo[1,2-a]pyridines via an efficient Grignard reagent-promoted 6-endo-dig cyclization of nitrile to alkynes. A previous optimization of the Sonogashir

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