70156-40-0

Usage

Uses

Used in Pharmaceutical Industry:
Methyl 3-[(4-Hydroxyphenyl)aMino]propanoate is used as an intermediate in the synthesis of pharmaceutical drugs for treating neurological disorders and cardiovascular diseases. Its ability to act as both an electron donor and acceptor makes it a valuable component in the development of these drugs.
Used in Agricultural Industry:
Methyl 3-[(4-Hydroxyphenyl)aMino]propanoate is also used in the production of many agricultural chemicals, such as pesticides and fertilizers. Its role in these products contributes to the effectiveness and performance of these agricultural chemicals.
Safety Precautions:
It is important to handle Methyl 3-[(4-Hydroxyphenyl)aMino]propanoate with care as it can be harmful if ingested, inhaled, or comes into contact with the skin. Proper safety measures should be taken during its production, use, and disposal to minimize any potential risks to human health and the environment.

Upstream product

• 123-30-8 4-amino-phenol 
• 292638-85-8 acrylic acid methyl ester 

Downstream Products

• 83809-75-0 1-(4-hydroxyphenyl)dihydropyrimidine-2,4(1H,3H)-dione 
• 84440-08-4 1-(4-acetoxyphenyl)-2-thiodihydrouracil 
• 84440-05-1 1-(4-acetoxyphenyl)dihydrouracil 
• 84440-11-9 1-(4-allyloxyphenyl)dihydrouracil 
• 84440-14-2 1-(4-methoxyphenyl)-3-methyldihydrouracil 
• 84439-95-2 1-(4-hydroxyphenyl)-2-thio-5,6-dihydrouracil 
• 84440-01-7 N-(4-hydroxyphenyl)-N-thiocarbamido-β-alanine 
• 84439-98-5 N-(4-hydroxyphenyl)-N-carbamido-β-alanine 
• 32987-42-1 N-(4-hydroxyphenyl)-β-alanine 
• 84439-92-9 N-(4-hydroxyphenyl)-β-alanine hydrazide 

Relevant academic research and scientific papers

Bio-heterogeneous Cu(0)NC@PHA for n-aryl/alkylation at room temperature

A pure cellulose was derived from waste fibre and it was chemically modified to a hydroxamic acid ligand. The poly(hydroxamic acid) was treated with an aqueous copper solution to afford the greenish stable five-membered copper complex; namely Cu(II)@PHA. Further, the Cu(II)@PHA was treated with a reducing agent hydrazine hydride to give brown colour cellulose supported copper nanocomplex (Cu(0)NC@PHA). The Cu(0)NC@PHA was characterised by ATR-FTIR, FE-SEM & EDS, TEM, ICP-OES, TGA, XRD and XPS analyses. The cellulose-based Cu(0)NC@PHA was used for the n-aryl/alkylation (Michael addition) reaction with a variety of α,β-unsaturated Michael acceptors to produce the corresponding n-aryl/alkyl products with an excellent yield at room temperature. The Cu(0)NC@PHA showed extraordinary stability and it was easily filtered out from the reaction mixture and may potentially recycled up to five times without loss of its original catalytic ability.

"On-water" conjugate additions of anilines

The conjugate addition of anilines onto unsaturated ketones, esters and N-acylpyrroles was investigated. Based on a recently proposed explanation for the phenomenon of on-water catalysis, operationally simple and mild reaction conditions for effecting these addition reactions have been developed. The success of these additions provides further support for the acid-catalysed nature of on-water chemistry.

SYNTHESIS AND TRANSFORMATIONS OF 1-(4-HYDROXYPHENYL)DIHYDROURACILS

N-(4-hydroxyphenyl)-β-alanine and its methyl derivatives, as well as p-hydroxy-phenylamino-β,β'-dipropionic acid, were obtained by the reaction of p-aminophenol with methyl acrylate and acrylic, methacrylic, and crotonic acids.The β-alanines were converte