22280-95-1

Usage

InChI:InChI=1/C11H12O3/c1-3-6-14-10-5-4-9(8-12)7-11(10)13-2/h3-5,7-8H,1,6H2,2H3

Upstream product

• 121-33-5 vanillin 
• 1044844-34-9 1-(allyloxy)-4-(azidomethyl)-2-methoxybenzene 
• 86534-11-4 3-methoxy-4-(2-propenyloxy) benzenemethanol 
• 139-85-5 3,4-dihydroxybenzaldehyde 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 79822-65-4 3-hydroxy-4-(2-propenyloxy)benzaldehyde 
• 74-88-4 methyl iodide 
• 106-95-6 allyl bromide 

Downstream Products

• 20240-58-8 3-allyl-4-hydroxy-5-methoxybenzaldehyde 
• 99661-58-2 (E)-3-(4-Allyloxy-3-methoxy-phenyl)-thioacrylamide 
• 263138-68-7 4-allyloxy-3-methoxyoxyphenol 
• 121-33-5 vanillin 
• 86534-11-4 3-methoxy-4-(2-propenyloxy) benzenemethanol 
• 1447973-47-8 C₁₁H₁₂O₄ 
• 1609627-88-4 (2E)-3-[4-hydroxy-3-methoxy-5-(prop-2-en-1-yl)phenyl]-1-(4-hydroxyphenyl)prop-2-en-1-one 
• 1609627-89-5 (2E)-1-(4-chlorophenyl)-3-[4-hydroxy-3-methoxy-5-(prop-2-en-1-yl)phenyl]prop-2-en-1-one 
• 1609627-91-9 (2E)-1-(4-chlorophenyl)-3-[3,4-dimethoxy-5-(prop-2-en-1-yl)phenyl]prop-2-en-1-one 
• 1609627-93-1 (2E)-3-[3,4-dimethoxy-5-(prop-2-en-1-yl)phenyl]-1-(4-methoxyphenyl)prop-2-en-1-one 

Relevant academic research and scientific papers

A concise synthesis of (±)-methoxyfumimycin ethyl ester

The protecting-group-free synthesis of (±)-methoxyfumimycin ethyl ester, a potential bacterial peptide deformylase (PDF) inhibitor, is reported. The synthetic approach features a tandem Friedel-Crafts alkylation/lactonisation access as a key reaction to g

Synthesis and structural characterization of novel O-substituted phenolic and chalcone derivatives with antioxidant activity

A series of novel 4-O-alkyltriazolylphenolic derivatives is first synthesized with good to excellent yields via the click reaction of 3-methoxy-4-O-propargylbenzaldehyde or 3-allyl-4-O-propargylacetophenone and aromatic azide derivatives. Next, the chalco

Design, synthesis, characterization, and anticancer activity of a novel series of O-substituted chalcone derivatives

A new series of O-substituted chalcone derivatives bearing an/a allyl-, prenyl- or propargyl-substituent at different positions of rings A and B and their derivatives as drug leads, was designed, synthesized, and characterized. The chalcone derivatives we

Concise and Convergent Enantioselective Total Syntheses of (+)-and (-)-Fumimycin

The concise and convergent total syntheses of (+)-and (-)-Fumimycin have been achieved by taking advantage of strategies for the asymmetric aza-Friedel-Crafts reaction of a highly substituted hydroquinone and N-fumaryl ketimine generated from the correspo

Introducing the Tishchenko reaction into sustainable polymer chemistry

Taking advantage of the structural characteristics of lignin-derived phenolic compounds, a combination of the Williamson and Tishchenko reactions produced a series of new α,ω-diene functionalized carboxylic ester monomers from both petrochemical and renewable resources, which were applicable in subsequent thiol-ene click and acyclic diene metathesis (ADMET) polymerizations, providing a series of poly(thioether esters) and unsaturated aromatic-aliphatic polyesters with high molecular weights.

Synthesis of a Novel calix[4]resorcinarene-Chitosan hybrid

Synthesis of a novel calix[4]resorcinarene-chitosan hybrid using vanillin as raw material has been conducted. The synthesis was carried out in four steps i.e. (1) allylation of vanillin, (2) HCl-catalyzed condensation allyl vanillin with resorcinol, (3) c

Synthesis of the intermediate for fumimycin: A natural peptide deformylase inhibitor

Synthetic efforts toward the potential bacterial peptide deformylase inhibitor fumimycin are reported. The synthetic approach features a tandem Friedel-Crafts alkylation/lactonization access as key reaction to the α, α-disubstituted amino acid unit, and r

Iodine-DMSO catalyzed chemoselective oxidative aromatization and deallylation, nondeallylation of aryl allyl ether of tetrahydro-β-carboline

We have developed a simple method for the chemoselective aromatization of tetrahydro-β-carboline with selective nondeallylation O-allyl groups in the presence of iodine (100 mol %) in dimethyl sulfoxide/H2O2. A convergent approach toward the oxidative aromatization with selective deallylation (deprotection) of O-allyl-tetrahydro-β-carboline using iodine in dimethyl sulfoxide/HCl has been described. The present protocol contains cheap catalyst, easy work up, normal reaction conditions, and high selectivity.

Chemoselective and ligand-free aerobic oxidation of benzylic alcohols to carbonyl compounds using alumina-supported mesoporous nickel nanoparticle as an efficient recyclable heterogeneous catalyst

An economically efficient and operationally simple ligand-free protocol for the chemoselective oxidation of benzylic alcohols to carbonyl compounds has been developed using alumina-supported nickel nanoparticles as a stable recyclable heterogeneous catalyst along with potassium tert-butoxide in the presence of aerial oxygen as an eco-friendly oxidant. The aliphatic alcohols remained unaffected under the present condition. Excellent chemoselectivity has also been demonstrated through intermolecular and intramolecular competition experiments. This protocol accommodates a diverse range of substituents with the tolerance of various sensitive moieties during the reaction. The catalyst could be recovered by filtration and reused consecutively without any significant loss in the catalytic activity. Moreover, the heterogeneity of the catalyst has also been established by the “hot filtration method (Sheldon's test)”.

Preparation, characterization, antioxidant evaluation of new curcumin derivatives and effects of forming HSA-bound nanoparticles on the stability and activity

Curcumin (CCM) is a well-known active component, which has been studied extensively in food and medicine field since it showed various activities. However, some serious issues limit its application, for example, the extremely low solubility, stability and