7770-25-4

Usage

Molecular structure

The compound has a triaza-1-azoniatricyclo[3.3.1.1~3,7~]decane core with a 4-methoxyphenyl group attached to the carbon chain.

Classification

It is a quaternary ammonium compound.

Chemical and pharmaceutical applications

The compound is commonly used in various chemical and pharmaceutical applications.

Use as a reactant

It is often used as a reactant in organic synthesis.

Use as a catalyst

The compound can also be utilized as a catalyst for certain chemical reactions.

Unique molecular structure

The compound's unique molecular structure and functional groups make it valuable for a variety of research and industrial purposes.

Functional groups

The compound contains a 4-methoxyphenyl group and a 2-oxoethyl group.

Molecular weight

The molecular weight of the compound is approximately 296.41 g/mol.

Solubility

The compound is likely to be soluble in polar solvents such as water and methanol due to the presence of the 4-methoxyphenyl group and the triaza-1-azoniatricyclo[3.3.1.1~3,7~]decane core.

Upstream product

• 100-97-0 hexamethylenetetramine 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Downstream Products

• 3883-94-1 2-amino-4'-methoxyacetophenone hydrochloride 
• 151427-05-3 <2-(4'-methoxyphenyl)-2-oxoethyl>ammonium bromide 
• 151427-27-9 N-(4-methoxyphenacyl)-2,6-dimethylisonicotinamide 
• 932389-85-0 N-(2-(4-methoxyphenyl)-2-oxoethyl)isonicotinamide 
• 96753-33-2 2-(4-pyridyl)-5-(4-methoxyphenyl)-oxazole 
• 24294-82-4 2,5-bis(4-methoxyphenyl)pyrazine 
• 238073-94-4 N-{2′-(4′′-methoxyphenyl)-2′-oxoethyl}-1-tosylpyrrole-2-carboxamide 
• 238073-95-5 5-(4′′-methoxyphenyl)-2-(1′-tosylpyrrol-2′-yl)-1,3-oxazole 
• 238073-96-6 5-(4′′-methoxyphenyl)-2-(pyrrol-2′-yl)-1,3-oxazole 

Relevant academic research and scientific papers

Synthesis of a New Phorbazole and Its Derivatives

Phorbazoles are chlorinated marine alkaloids containing pyrrole, oxazole and phenol ring units, and differ in the number and positions of chlorine atoms. They are isolated from sea sponges and nudibranchs. In this work, a convenient synthetic method leading to a new phorbazole and its derivatives is developed. This synthesis of synthetic phorbazole G and its derivatives is achieved in seven steps in good overall yields of 26-52%. It involves formation of the pyrrole-oxazole skeleton followed by chlorination. The pyrrole-oxazole skeleton is synthesized from pyrrole and substituted acetophenones, and the key step involves cyclodehydration of amide intermediates to give protected oxazoles, followed by hydrolysis.

Synthesis, characterization, COX1/2 inhibition and molecular modeling studies on novel 2-thio-diarylimidazoles

Heterocyclic compounds with diaryl substituents have been a milestone approach for selective cyclooxygenase 2 (COX 2) inhibition by bioisosteric replacements and modifications. It is also known that thiazole derivatives have different pharmacological acti

Investigations into the parallel synthesis of novel pyrrole-oxazole analogues of the insecticide pirate

Investigations into the parallel synthesis of selected analogues of a structurally unique pyrrole-oxazole analogue of the pyrrole insecticide pirate, are reported. Acylaminoketone salts were obtained from ketobromides in moderate to high yields and excell

1-[[[5-(Substituted phenyl)-2-oxazolyl]methylene]amino]-2,4-imidazolidinediones

A series of 1-[[[5-(substituted phenyl-2-oxazolyl]methylene]amino]-2,4-imidazolidinediones are useful as muscle relaxants.