22727-22-6

Usage

Uses

Used in Pharmaceutical Research and Drug Development:
2-Methylfuran-3-carboxyamide serves as a valuable compound in pharmaceutical research and drug development due to its potential biological activity and therapeutic properties. It is utilized for its capacity to be a key component in the creation of new medications.
Used in Medical Treatments:
In the medical field, 2-Methylfuran-3-carboxyamide is explored for its potential use in treating various conditions, such as cancer and neurological disorders. Its therapeutic properties make it a promising candidate for further research and development in these areas.
Used as a Building Block in Organic Synthesis:
Furthermore, 2-Methylfuran-3-carboxyamide is recognized for its potential as a building block in the synthesis of other organic compounds. This quality positions it as a valuable tool in medicinal chemistry and drug discovery, contributing to the advancement of new chemical entities and therapeutic agents.

Upstream product

• 5555-00-0 2-methylfuran-3-carbonyl chloride 
• 6141-58-8 methyl 2-methyl-3-furancarboxylate 

Downstream Products

• 35801-15-1 (2-methylfuran-3-yl)methanamine 

Relevant academic research and scientific papers

Novel flavors, flavor modifiers, tastants, taste enhancers, umami or sweet tastants, and/or enhancers and use thereof

The present invention relates to the discovery that certain non-naturally occurring, non-peptide amide compounds and amide derivatives, such as oxalamides, ureas, and acrylamides, are useful flavor or taste modifiers, such as a flavoring or flavoring agents and flavor or taste enhancer, more particularly, savory (the “umami” taste of monosodium glutamate) or sweet taste modifiers,—savory or sweet flavoring agents and savory or sweet flavor enhancers, for food, beverages, and other comestible or orally administered medicinal products or compositions.

Anti-Helicobacter pylori agents. 3. 2-[(Arylalkyl)guanidino]-4- furylthiazoles

A series of 2-[(arylalkyl)guanidino]-4-[(5-acetamidomethyl)furan-2- yl]thiazoles and some 4-acetamidomethyl positional isomers were synthesized and evaluated for antimicrobial activity against Helicobacter pylori. Among the compounds that had potent antim

A MILD EFFICIENT PROCEDURE FOR THE CONVERSION OF CARBOXYLIC ACID ESTERS TO PRIMARY AMIDES USING FORMAMIDE/METHANOLIC SODIUM METHOXIDE

An improved method for the preparation of primary carboxylic acid amides from the corresponding esters is described.This reaction was easily followed by GLC and was usually complete in less than one hour.