22469-15-4

Basic information

• Product Name: (E)-3-(2-aminophenyl)-2-propenoic acid
• Synonyms: (E)-3-(2-aminophenyl)-2-propenoic acid
• CAS NO: 22469-15-4
• Molecular Weight: 163.176
• Mol File: 22469-15-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (E)-3-(2-aminophenyl)-2-propenoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(2-aminophenyl)-2-propenoic acid(22469-15-4)
• EPA Substance Registry System: (E)-3-(2-aminophenyl)-2-propenoic acid(22469-15-4)

Safety Data

• Hazardous Substances Data: 22469-15-4(Hazardous Substances Data)

Upstream product

• 615-43-0 2-iodophenylamine 
• 79-10-7 acrylic acid 
• 88939-75-7 methyl (2E)-3-(2-aminophenyl)propenoate 
• 39228-29-0 (E)-methyl 2-nitrocinnamate 
• 1758-83-4 2-aminophenyl-L-alanine 
• 552-89-6 2-nitro-benzaldehyde 
• 40515-78-4 (E)-3-(2-azidophenyl)acrylic acid 
• 127-09-3 sodium acetate 
• 64-19-7 acetic acid 
• 612-41-9 2-nitrocinnamic acid 
• 7647-01-0 hydrogenchloride 
• 64-17-5 ethanol 
• 144402-63-1 trans-2-carbamoylcinnamic acid 
• 615-36-1 2-bromoaniline 

Downstream Products

• 342-19-8 (2RS:3SR)-2,3-dibromo-3-(2-fluoro-phenyl)-propionic acid 
• 621-82-9 Cinnamic acid 
• 59-31-4 2-quinolone 
• 92855-96-4 2-benzoylamino-cinnamic acid 
• 10168-37-3 N-(2-quinolyl)-2-quinolone 
• 103989-08-8 alpha-acetaminocinnamic acid 
• 40515-78-4 (E)-3-(2-azidophenyl)acrylic acid 
• 18944-77-9 2-fluorocinnamic acid 

Relevant articles and documents

Oxime-derived palladacycle Immobilized in an Ionic Liquid Brush as an Efficient and Reusable Catalyst for Mozoroki-Heck Reaction in Neat Water

An efficient and reusable heterogeneous catalyst with oxime-derived palladacycle immobilized in an ionic liquid brush has been synthesized and an environmentally-friendly procedure have been developed for coupling aryl iodides and bromides with acrylic acid. These reactions were conducted in neat water under aerobic conditions with water-insoluble or even solid aryl halides and they proceeded smoothly and cleanly without any organic co-solvent or other additives. The ionic liquid brush could be easily recovered and reused at least five times without significant loss of activity. The protocol has the advantages of excellent yields, environmental friendliness, and catalyst recyclability.

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

Indium-mediated reductive cyclizations in aqueous ethanol: Highly efficient synthesis of heterocyclic compounds of biological interests

Indium/ammonium chloride in the presence of aqueous ethanol was found to be very effective in reductive cyclization reactions leading to the development of several heterocyclic compounds of biological significance.