17570-30-8

Basic information

• Product Name: 4-Aminocinnamic acid
• Synonyms: 4-Amino-trans-cinnamic acid;(E)-3-(4-aminophenyl)acrylic acid;(E)-4-Aminocinnamic Acid
• CAS NO: 17570-30-8
• Molecular Formula: C₉H₉NO₂
• Molecular Weight: 163.17
• Mol File: 17570-30-8.mol
• Article Data: 10

Chemical Properties

• Melting Point: 170 °C
• Boiling Point: 378.4±25.0 °C(Predicted)
• Appearance: /
• Density: 1.281±0.06 g/cm3(Predicted)
• PKA: 5.37±0.10(Predicted)
• CAS DataBase Reference: 4-Aminocinnamic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Aminocinnamic acid(17570-30-8)
• EPA Substance Registry System: 4-Aminocinnamic acid(17570-30-8)

Safety Data

• RTECS: UD3000000
• Hazardous Substances Data: 17570-30-8(Hazardous Substances Data)

Usage

General Description

4-Aminocinnamic acid is a chemical compound that belongs to the family of cinnamic acids, and it is characterized by the presence of an amino group (NH2) on the 4-position of the cinnamic acid molecule. 4-Aminocinnamic acid is widely utilized in the field of organic synthesis and pharmaceutical research due to its potential pharmacological activities, including anti-inflammatory, antimicrobial, and antioxidant properties. It also has been studied for its potential role in the treatment of various diseases, such as cancer and diabetes. Additionally, 4-Aminocinnamic acid has been used as a building block in the synthesis of various biologically active compounds and as a precursor in the production of dyes and pigments.

Upstream product

• 882-06-4 4-nitro-trans-cinnamic acid 
• 64-17-5 ethanol 
• 133463-51-1 (E)-3-(4-azidophenyl)acrylic acid 
• 7647-01-0 hydrogenchloride 
• 2922-41-0 (p-aminophenyl)alanine 
• 64-19-7 acetic acid 
• 144072-30-0 4-((tert-butoxycarbonyl)amino)benzaldehyde 
• 77120-14-0 (E)-3-(4-aminophenyl)acrylonitrile 
• 67249-02-9 (E)-3-(4-acetylaminophenyl)acrylic acid 

Downstream Products

• 66417-26-3 methyl (2E)-3-(4-aminophenyl)acrylate 
• 197073-43-1 4-(tert-butyloxycarbonylamino)cinnamic acid 
• 119348-97-9 4-amino-cinnamic acid methyl ester; hydrochloride 
• 331734-29-3 (4-(4-(2-carboxy)ethenyl)anilino)-6,7-dimethoxyquinazoline 
• 283153-80-0 4-(trifluoroacetylamino)cinnamic acid 
• 1310877-48-5 (2E,2'E)-3,3'-(((6-(trifluoromethyl)quinoxaline-2,3-diyl)bis-(azanediyl))bis(4,1-phenylene))diacrylic acid 
• 174603-71-5 N-[4-(2-carboxy-(E)-ethenyl)phenyl]maleimide 

Relevant articles and documents

Activated carbon as an efficient support for gold nanoparticles that catalyze the hydrogenation of nitro compounds with molecular hydrogen

A catalyst based on activated carbon with deposited gold nanoparticles and impregnated with ethylenediamine for selective hydrogenation of nitroarenes has been suggested.

4-AMINO CINNAMIC ACID PRODUCTION METHOD USING ENZYME

This 4-amino cinnamic acid production method using the enzyme ammonia lyase can efficiently convert 4-amino phenylalanine into 4-amino cinnamic acid. This 4-amino cinnamic acid production method is characterized by converting 4-amino phenylalanine into 4-amino cinnamic acid by using phenylalanine ammonia-lyase, which comprises the amino acid sequence represented in sequence number 2 derived from the Rhodotorula glutinis yeast.

Stereoselective synthesis of phenyl-1,2,3-triazoles containing (E)-vinyl halide group via a one-pot, three-component reaction

Phenyl-1,2,3-triazoles containing (E)-vinyl halide were readily synthesized via a one-pot, three-component reaction of 3-(4- or 2-azidophenyl)acrylic acid, NXS(X=Cl, Br and I) and 1-alkynes in MeCN-H2O (9:1v/v) catalyzed by LiOAc/CuI-sodium ascorbate syst