41065-01-4

Usage

Derivative of imidazole

The compound is a derivative of imidazole, a five-membered heterocyclic ring containing three carbon atoms and two nitrogen atoms.

Versatile reactivity

1H-Imidazole-5-acetonitrile, 1-methyl-(9CI) is commonly used in organic synthesis and pharmaceutical research due to its ability to react in various ways.

Potential biological activities

The compound has potential biological activities, making it a valuable tool for studying the reactivity and biological effects of imidazole derivatives.

Building block in synthesis

The compound can be utilized as a building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials.

Upstream product

• 773837-37-9 sodium cyanide 
• 38993-84-9 (1-methyl-1H-imidazol-5-yl)methanol 
• 151-50-8 potassium cyanide 
• 90773-41-4 5-chloromethyl-1-methyl-1H-imidazole hydrochloride 
• 18502-05-1 4-cyanomethylimidazole 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 644-42-8 3-methylhistamine 

Relevant academic research and scientific papers

Synthesis of Conformationally Locked and C-Linked Analogues of Imidazole-Based Ketene Dithioacetal Fungicides

First examples with the unknown tricyclic 4,8 b -dihydro-3 aH -indeno[1,2- d ][1,3]dithiole ring system have been prepared. Also, imidazoles linked in ring position 5 to a ketene dithioacetal and 1,3-dithiane derivatives with an exocyclic cyano- and imidazole-substituted C-C double bond are completely new. All these compounds are either conformationally locked, C-linked or six-ring analogues of the antifungal agent luliconazole. Synthesis and fungicidal activity of these sterol biosynthesis inhibitors are reported.

Condensed thiazole derivative, production process thereof and pharmaceutical composition thereof

Condensed thiazole derivatives useful as 5-HT3 receptor agonists are provided and can be represented by the following formula (I) or a pharmaceutically acceptable salt thereof, a process for the production thereof and a pharmaceutical composition thereof: STR1 wherein R, A, L1, L2, L, and R1 -R6 are defined herein and Im represents a group of the formula: STR2