202282-59-5

Usage

Uses

Used in Chemical and Pharmaceutical Industries:
1H-Imidazolium,2-[[bis(dimethylamino)methylene]amino]-4,5-dihydro-1,3-dimethyl-,chloride is used as a catalyst in organic synthesis reactions for its ability to facilitate certain chemical transformations, enhancing the efficiency and selectivity of these processes.
Used in Antimicrobial and Antifungal Applications:
Due to its potential antimicrobial and antifungal properties, 1H-Imidazolium,2-[[bis(dimethylamino)methylene]amino]-4,5-dihydro-1,3-dimethyl-,chloride can be utilized in various applications where control of microbial growth is necessary, such as in the development of new antimicrobial agents or in the preservation of materials.
It is important to handle 1H-Imidazolium,2-[[bis(dimethylamino)methylene]amino]-4,5-dihydro-1,3-dimethyl-,chloride with caution, as it may pose certain risks to human health and the environment.

Upstream product

• 80-73-9 1,3-dimethyl-2-imidazolidinone 
• 80-70-6 N,N,N',N'-tetramethylguanidine 
• 343927-22-0 2,2-dichloro-1,3-dimethylimidazolidine 
• 37091-73-9 2-chloro-1,3-dimethylimidazolinium chloride 

Relevant academic research and scientific papers

ACID-RESISTANT BASE AND/OR RADICAL GENERATOR, AND CURABLE RESIN COMPOSITION CONTAINING SAID BASE AND/OR RADICAL GENERATOR

The present invention relates to a compound represented by the general formula (A), a base- and/or radical-generating agent comprising the compound, and so on. In the formula, four pieces of R1 each independently represents a hydrogen atom or a

BORATE-BASED BASE GENERATOR, AND BASE-REACTIVE COMPOSITION COMPRISING SUCH BASE GENERATOR

An object of the present invention is to provide a compound which is capable of attaining a composition having high storage stability without reacting with a base-reactive compound, even in the case of storage for a long period of time in a mixed state wi

Process for preparing ring-fluorinated aromatics

The present invention relates to an improved process for preparing ring-fluorinated aromatics of the general formula (I) by a halogen exchange reaction (halex reaction) of a plurality of halogen substituents in one stage in the presence of a catalyst.

Halex reactions of aromatic compounds catalysed by 2-azaallenium, carbophosphazenium, aminophosphonium and diphosphazenium salts: A comparative study

An increasing number of biologically active compounds in the pharma and agro-chemical sector contain carbon fluorine bonds. One of the most common methods to introduce fluorine into intermediates is the well-investigated halogen-exchange reaction, in which chloro- and bromoaromatics activated towards nucleophilic substitution, react with a fluoride source to yield the corresponding fluoroarenes. In general, the reaction is supported by phase-transfer catalysts. The use of a new class of very active phase-transfer catalysts gives the possibility of substituting even halogens with weak activation giving a convenient access to interesting compounds that are not available so far and opening up new synthetic routes in Halex chemistry. Our new classes of catalysts, CNC+ (1a), PNC+ (2a) and several different approaches presented by other groups are described and experimental results discussed.