4792-57-8

Usage

Uses

Used in Pharmaceutical Industry:
Ethyl (E)-2-(2-(4-methoxyphenyl)hydrazono)propanoate is used as a pharmaceutical candidate for the development of new drugs due to its antioxidant and anti-inflammatory properties. It has shown potential in research related to the prevention and treatment of various diseases, making it a valuable asset in drug discovery and formulation.
Used in Cosmetic Industry:
In the cosmetic industry, ethyl (E)-2-(2-(4-methoxyphenyl)hydrazono)propanoate is used as an active ingredient in skincare products. Its antioxidant and anti-inflammatory properties contribute to the development of formulations that promote skin health and address various skin concerns, such as inflammation and oxidative stress.
Used in Research:
Ethyl (E)-2-(2-(4-methoxyphenyl)hydrazono)propanoate is also utilized in research settings to explore its potential role in preventing and treating various diseases. Its antioxidant and anti-inflammatory properties make it a promising candidate for further investigation and development in the field of medicine.

Upstream product

• 609-14-3 2-acetylpropanoic acid ethyl ester 
• 459-64-3 4-methoxybenzenediazonium tetrafluoroborate 
• 617-35-6 2-oxo-propionic acid ethyl ester 
• 19501-58-7 4-methoxyphenylhydrazine hydrochloride 
• 89693-83-4 N-Nitroso-p-methoxyanilin 
• 4792-56-7 ethyl 2-(4-methoxyphenylazo)-2-methyl-3-oxobutanoate 
• 4346-59-2 para-methoxyphenyldiazonium chloride 
• 104-94-9 4-methoxy-aniline 
• 17333-79-8 p-methoxybenzenediazonium 

Downstream Products

• 4792-58-9 ethyl 5-methoxy-1H-indole-2-carboxylate 
• 1159692-52-0 4-formyl-1-(4-methoxyphenyl)-1H-pyrazole-3-carboxylic acid 
• 1159691-45-8 ethyl 4-formyl-1-(4-methoxyphenyl)-1H-pyrazole-3-carboxylate 
• 4382-54-1 5-methoxy-1H-indole-2-carboxylic acid 

Relevant academic research and scientific papers

Rh(II)-catalyzed intramolecular annulation of N-sulfonyl 1,2,3-triazoles with indole derivatives: A new method for synthesis pyranoindoles

A direct and highly stereoselective approach for the synthesis of Z-alkenyl-pyranoindoles had been developed by utilizing Rh(II)-catalyzed intramolecular cyclization of N-sulfonyl-1,2,3-triazoles with indole derivatives. A variety of pyranoindoles were obtained in 44-93% yields. Moreover, a more convenient synthesis of pyranoindoles starting from terminal alkyne was realized via a Cu-Rh sequentially catalyzed one-pot cascade reaction.

A simple and efficient synthesis of ethyl 1-Aryl-4-formyl-1H-pyrazole-3- carboxylates

A new simple and convenient method of synthesis of ethyl 1-aryl-4-formyl-1H-pyrazole-3-carboxylates from aromatic amines via diazonium salts has been developed. Hydrolysis and hydrazinolyization of these compounds has been investigated.

Process development of 5-methoxy-1H-indole-2-carboxylic acid from ethyl 2-methylmalonate

Development is described of a new process for the preparation from malonates of 5-methoxy-1H-indole-2-carboxylic acid esters, useful intermediates in the synthesis of pharmaceutical compounds. The process uses readily available starting materials, produces little waste, can be operated safely on at least 1 molar scale, and gives high yields. The main areas of optimization included the azo coupling of a diazonium salt with malonate derivatives, the Japp-Klingemann rearrangement, and the Fischer indole synthesis.