1664-63-7

Usage

Uses

Used in Organic Synthesis:
2-Aminocinnamic acid is used as a building block in organic synthesis for the production of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and properties make it a valuable component in the development of new drugs and therapeutic agents.
Used in Pharmaceutical Industry:
2-Aminocinnamic acid is used as a precursor in the synthesis of pharmaceuticals for its potential biological properties, including anti-inflammatory and anti-cancer activities. Its presence in the development of new drugs and therapeutic agents highlights its importance in the medical field.
Used in Agrochemical Industry:
2-Aminocinnamic acid is utilized as a key component in the creation of agrochemicals, where its unique structure contributes to the effectiveness of these compounds in agricultural applications.
Used in Functional Materials:
2-Aminocinnamic acid is employed in the development of functional materials, where its chemical properties can be harnessed to create materials with specific characteristics for various applications.

InChI:InChI=1/C9H9NO2/c10-8-4-2-1-3-7(8)5-6-9(11)12/h1-6H,10H2,(H,11,12)/b6-5+

Upstream product

• 61147-65-7 2-cyano-cinnamic acid 
• 58106-56-2 ethyl (E)-3-(2-aminophenyl)acrylate 
• 612-41-9 2-nitrocinnamic acid 
• 7664-41-7 ammonia 
• 14380-61-1 hypochlorite 
• 70321-33-4 2,3-dibromo-3-(2-nitrophenyl)propanoic acid 
• 64-19-7 acetic acid 
• 615-43-0 2-iodophenylamine 
• 79-10-7 acrylic acid 
• 2437-05-0 ethyl 3-(2-nitrophenyl)acrylate 

Downstream Products

• 614-60-8 o-Coumaric acid 
• 3752-25-8 o-chlorocinnamic acid 
• 451-69-4 2-fluorocinnamic acid 
• 140-10-3 (E)-3-phenylacrylic acid 
• 7345-79-1 2-bromocinnamic acid 
• 61147-65-7 2-cyano-cinnamic acid 
• 59-31-4 2-quinolone 
• 90276-19-0 (E)-3-(2-Iodophenyl)propenoic acid 
• 81536-29-0 2-mercaptocinnamic acid 
• 116557-35-8 2-amino-4-nitro-cinnamic acid 
• 126263-76-1 (E)-3-[2-(4,5-Dimethyl-3-oxy-imidazol-1-yl)-phenyl]-acrylic acid 
• 29848-08-6 (E)-3-[2-(3,4-Dichloro-benzoylamino)-phenyl]-acrylic acid 

Relevant academic research and scientific papers

Rapid and efficient synthesis of 2-amino-4H-benzothiazines

(matrix presented) The benzothiazine nucleus is a relatively unexplored class of compounds, from the standpoint of both synthetic chemistry and biological activity. We have developed a rapid, high-yielding synthesis of benzothiazines in which a precursor

Recyclable glucose-derived palladium(0) nanoparticles as in situ-formed catalysts for cross-coupling reactions in aqueous media

In situ-generated, glucose-derived palladium(0) nanoparticles were shown to be convenient and effective catalysts for aqueous Mizoroki-Heck, Sonogashira and Suzuki-Miyaura cross-coupling reactions. The addition of only 4-10 mol% glucose to the reaction mixture lead to a significant increase in yield of the desired products in comparison to processes that omitted the renewable sugar. Interestingly, the Mizoroki-Heck reaction was observed to proceed in good yield even as the reaction reached acidic pH levels. Extensive analysis of the size and morphology of the in situ-formed palladium nanoparticles using advanced analytical techniques showed that the zero valent metal was surrounded by hydrophilic hydroxyl groups. The increased aqueous phase affinity afforded by these groups allowed for facile recycling of the catalyst.

RuCl2(PPh3)3/HCOOH/Et3N AS A NEW HYDROGEN SOURCE. SELECTIVE REDUCTION OF AROMATIC NITRO COMPOUNDS CATALYSED BY Pd ON CARBON

Pd on carbon increases the reactivity of the system RuCl2(PPh3)3/HCOOH/Et3N and induces selective reduction of nitroaromatic compounds which is faster than that of olefins or haloaromatic derivatives.Other potentially reducible groups do not react.