55620-18-3

Usage

Uses

Used in Pharmaceutical Industry:
2-ACETOXYCINNAMIC ACID is used as an intermediate in the synthesis of various pharmaceuticals for its potential anti-inflammatory and antioxidant properties. It contributes to the development of medications that can address a range of health conditions by reducing inflammation and oxidative stress.
Used in Agrochemical Industry:
In the agrochemical sector, 2-ACETOXYCINNAMIC ACID is utilized as a precursor in the production of agrochemicals, potentially enhancing crop protection and yield through its incorporation into various formulations.
Used in Cosmetic Products:
2-ACETOXYCINNAMIC ACID is used as an active ingredient in cosmetic products for its potential anti-aging effects. Its ability to combat oxidative stress and inflammation makes it a promising component in skincare and beauty formulations aimed at promoting healthier and younger-looking skin.
Used in Cancer Treatment Research:
2-ACETOXYCINNAMIC ACID is studied for its potential role in cancer treatment. Its anti-inflammatory and antioxidant properties are being investigated for their possible contribution to the mitigation of cancer progression and the enhancement of therapeutic strategies.
Used in Organic Chemistry Research:
As a valuable tool in organic chemistry, 2-ACETOXYCINNAMIC ACID is used in various research applications to explore its chemical properties and potential reactions, paving the way for the discovery of new compounds and applications.

InChI:InChI=1/C11H10O4/c1-8(12)15-10-5-3-2-4-9(10)6-7-11(13)14/h2-7H,1H3,(H,13,14)/b7-6+

Upstream product

• 5663-67-2 2-acetoxybenzaldehyde 
• 90-02-8 salicylaldehyde 
• 69232-65-1 tert-butyl 2-hydroxycinnamate 
• 463-51-4 Ketene 
• 127-09-3 sodium acetate 
• 67-64-1 acetone 

Downstream Products

• 75746-62-2 o-Acetoxyzimtsaeuremethylester 
• 33538-94-2 3-(2'-O-acetylphenyl)-2-propenal 
• 1451377-34-6 C₁₃H₁₃NO₃ 
• 20996-40-1 2-Acetoxy-cinnamoylchlorid 
• 1219038-82-0 methyl Nα-[3-(2-acetoxyphenyl)acryloyl]-L-tryptophanate 

Relevant academic research and scientific papers

Effective synthesis of cyclic peptide yunnanin C and analogues via Ser/Thr ligation (STL)-mediated peptide cyclization

Cyclic peptide yunnanin C isolated from the root of Stellaria yunnanensis was efficiently synthesized in which the linear peptide was prepared by Boc-SPPS and the cyclization was realized by serine/threonine ligation (STL)-mediated cyclization. In addition, nine yunnanin C analogues, including mutations of Tyr7Gly, Tyr7Val, Tyr7Pro, Tyr7Phe, Ser1Thr, Pro2Val, Gly5Pro, Phe6Ala and Ile4Ala, were prepared in the same fashion. Here, we demonstrated that STL-mediated peptide cyclization could be an effective approach to construct cyclic peptides. Except that proline at the C-terminus could retard the cyclization process, cyclization of yunnanin C analogues with various C-terminal amino acids proceeded with fast cyclization rate (a working concentration of 5 mM.

Synthesis of constrained head-to-tail cyclic tetrapeptides by an imine-induced ring-closing/contraction strategy

Making heads or tails of it: A strategy involving a head-to-tail imine-captured ring closure followed by ring contraction was used to synthesize otherwise difficult cyclic tetrapeptides. Compared with the direct lactamization process, the estimated activa

Effective synthesis of kynurenine-containing peptides via on-resin ozonolysis of tryptophan residues: Synthesis of cyclomontanin B

The preparation of Kyn-containing peptides is difficult, owing to the low reactivity of Kyn in the coupling reaction. In this report, Kyn-containing peptides were efficiently obtained via on-resin ozonolysis of the corresponding Trp-containing peptide. In