43129-93-7

Usage

Uses

Used in Polymer and Copolymer Production:
2-Vinylimidazole is used as a monomer for the production of polymers and copolymers, contributing to the development of materials with specific properties and applications.
Used as a Crosslinking Agent:
In industries such as adhesives, coatings, and textile treatments, 2-Vinylimidazole serves as a crosslinking agent. This role enhances the performance and durability of the final products by strengthening the bonds between polymer chains.
Used in Pharmaceutical Applications:
2-Vinylimidazole has potential uses in the pharmaceutical industry, capitalizing on its ability to form complexes with metal ions and its biological activity. This can lead to the development of new drugs or drug delivery systems.
Used in Cosmetics and Personal Care Products:
2-VINYLIMIDAZOLE also finds application in cosmetics and personal care products, where its metal-ion complexing properties and biological activity can be harnessed to improve product performance or provide specific benefits to users.
It is crucial to handle and use 2-Vinylimidazole with care, as it is considered a hazardous chemical. Precautions should be taken to protect against exposure to ensure the safety of individuals and the environment.

InChI:InChI=1/C5H6N2/c1-2-5-6-3-4-7-5/h2-4H,1H2,(H,6,7)

Upstream product

• 51036-79-4 2-(2-Hydroxyethyl)imidazole 
• 91937-77-8 2-(5-Norbornen-2-yl)imidazol 
• 1174192-08-5 1-trityl-2-vinyl-1H-imidazole 
• 2065-66-9 methyl-triphenylphosphonium iodide 
• 10111-08-7 2-imidazolecarbaldehyde 

Downstream Products

• 802296-13-5 2-(1H-imidazol-2-yl)-N,N-dimethylethanamine 

Relevant academic research and scientific papers

AMPHIPHOBIC POROUS MATERIALS

A variety of amphiphobic porous materials are provided. The materials can include a variety of porous frameworks that have an outer surface functionalized by a plurality of perfluoroalkyl moieties. By careful selection of appropriate perfluoralkyl moieties, hydrophobic properties can be imparted to the exterior surface of the porous materials without significantly impacting the wetting properties of the porous interior. This can be used to create a variety of highly amphiphobic porous materials. Methods of making and using the amphiphobic porous materials are also provided.

TRIAZINE COMPOUNDS AS KINASE INHIBITORS

The present invention relates to triazine compounds that are useful as kinase inhibitors. More particularly, the present invention relates to morpholino substituted triazines, methods for their preparation, pharmaceutical compositions containing these compounds and uses of these compounds in the treatment of proliferative disorders. These compounds may be useful as medicaments for the treatment of a number of proliferative disorders including tumours and cancers as well as other disorders or conditions related to or associated with mTOR kinases or PI3 kinases. The compounds are of the formula (I)

Color developing agent, processing composition and color image-forming method

A method for forming a color image comprises the step of developing an image-wise exposed silver halide color photographic photosensitive material at the presence of a 6-aminotetrahydroquinoline color developing agent which is the following compound or its analoge. According to this method, the rapid process can be attained and an image of a low fog density can be obtained. STR1

The Structure of +. and + Ions Formed from Vinylimidazoles, Studied by Collisionally Activated Dissociation Mass Spectrometry

Mass spectra of the three isomeric vinylimidazoles have been compared and the structures of the fragment ions +. and + have been investigated by collisionally activated dissociation mass spectrometry.The greater part of the non-decomposing ions m/z 68 from 2-vinylimidazole and from 2-imidazolecarboxylic acid methyl ester, and a minor part of this ion formed from the free acid, all have the same structure: the imidazole ring system, with hydrogens at both nitrogen atoms but none at C(2).An analogous structure, with an ethynyl group at C(2), is proposed for the m/z 93 ion from 2-vinylimidazole.

Preparation of 2-vinylimidazoles by dehydrogenation of 2-ethylimidazoles and 2-ethylimidazolines

A method for preparing 2-alkenylimidazoles from readily available 2-alkylimidazoles or 2-alkylimidazolines by dehydrogenating the 2-alkylimidazole or 2-alkylimidazoline in the presence of a suitable dehydrogenation catalyst. The preferred method provides 2-vinylimidazole by dehydrogenating 2-ethylimidazole or 2-ethylimidazoline. The reaction is advantageously carried out in a vapor phase in the presence of an inert carrier gas using as preferred dehydrogenation catalysts, copper chromites and catalysts comprising one or more of the metals molybdenum, iron, cobalt, zinc or chromium on non-reducible oxide supports such as alumina or silica.