62397-61-9

Usage

Uses

Used in Organic Synthesis:
2,5-Dimethoxybenzenepropanoic acid methyl ester is used as a reagent in organic synthesis for its versatile reactivity and functional groups, enabling the creation of a wide range of chemical compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, 2,5-Dimethoxybenzenepropanoic acid methyl ester is used as a precursor for the synthesis of various psychoactive compounds, including designer drugs and hallucinogens, due to its unique chemical structure and properties.
Used in the Production of Pharmaceuticals:
2,5-Dimethoxybenzenepropanoic acid methyl ester is used as a building block in the production of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in the Production of Agrochemicals:
2,5-Dimethoxybenzenepropanoic acid methyl ester is also utilized in the production of agrochemicals, where its reactivity and functional groups are leveraged to create effective agricultural products.
Used in Regulatory Scrutiny:
Due to its potential for misuse and abuse, 2,5-Dimethoxybenzenepropanoic acid methyl ester is under regulatory scrutiny to ensure its use is controlled and monitored within the chemical and pharmaceutical industries.

InChI:InChI=1/C12H16O4/c1-14-10-5-6-11(15-2)9(8-10)4-7-12(13)16-3/h5-6,8H,4,7H2,1-3H3

Upstream product

• 292638-85-8 acrylic acid methyl ester 
• 150-78-7 1,4-dimethoxybezene 
• 116406-20-3 Methyl (E)-3-(2,5-Dimethoxyphenyl)propenoate 
• 28689-10-3 methyl 2,5-dimethoxycinnamate 

Downstream Products

• 251447-03-7 R_S-4-(2,5-dimethoxyphenyl)-1-p-tolylsulfinyl-2-butanone 
• 436155-33-8 3-(2,5-dimethoxyphenyl)propanoylhydrazine 
• 1116612-26-0 methyl 3-(3,6-dioxocyclohexa-1,4-dienyl)propanoate 
• 1000895-56-6 5-[2-(2,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine 
• 251447-07-1 (1S,2R,1'R),(1S,2R,1'S)-1,2,3,4-tetrahydro-2-(1-hydroxyethyl)-5,8-dimethoxy-O-trimethylsilyl-1-(p-tolylthio)-2-naphthol 
• 251447-08-2 (1S,2R)-(+)-1,2,3,4-tetrahydro-2-hydroxymethyl-5,8-dimethoxy-O-trimethylsilyl-1-p-tolylthio-2-naphthol 
• 251447-10-6 Toluene-4-sulfonic acid (R)-2-hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydro-naphthalen-2-ylmethyl ester 
• 251447-04-8 (2S,R_S)-2-cyano-4-(2,5-dimethoxyphenyl)-1-(p-tolylsulfinyl)-2-butanol 
• 41098-96-8 (R)-2-acetyl-2-hydroxy-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene 
• 436155-74-7 phenyl (6-hydroxy-7-methoxy-2-oxo-1,2,3,4-tetrahydroquinolin-1-yl)carbamate 
• 436155-46-3 phenyl 2-[3-(2,5-dimethoxyphenyl)propanoyl]hydrazinecarboxylate 
• 1225546-12-2 C₁₃H₁₅NO₃ 

Relevant academic research and scientific papers

Chemoselective reduction of α,β-unsaturated carbonyl compounds in the presence of CuPd alloy nanoparticles decorated on mesoporous graphitic carbon nitride as highly efficient catalyst

Herein, we reported reductions of acid, amide, ester and ketone groups with selectivity (>99%) by the catalytic transfer hydrogenation of with CuPd alloy nanoparticles (NPs) decorated on mesoporous graphitic carbon nitride (Cu50Pd50/mpg-C3N4) catalyst under mild conditions in a water/methanol mixture. CuPd alloy NPs were synthesized by the co-reduction of palladium (II) acetylacetonate and copper(II) acetylacetonate in oleylamine (OAm) solution by the reduction of morpholine-borane solution and then assembled on mpg-C3N4 via liquid phase self‐assembly method. The α, β-unsaturated carbonyl compounds were obtained from the condensation reaction of the benzaldehyde derivatives with acetone derivatives. Cu50Pd50/mpg-C3N4 nanocatalyst was characterized by TEM, XRD, XPS, BET and ICP‐MS. Cu50Pd50/mpg-C3N4 nanocatalyst is highly active catalyst for the reduction of various organic groups and converted to high yield and 99% selectivity. The superior Cu50Pd50/mpg-C3N4 nanocatalyst is highly efficient and reusable catalyst which is reuse after 5 cycle with 98% conversion.

Solid-supported green synthesis of substituted hydrocinnamic esters by focused microwave irradiation

An efficient chemoselective hydrogenation protocol for substituted cinnamic esters is developed for the synthesis in quantitative yield of corresponding bioactive dihydrocinnamic esters with solid-supported palladium chloride/ammonium formate (cat.) in HCOOH/H2O 1:2 as a hydrogenating agent under focused-microwave irradiation for 10 min.

A new stereocontrolled entry into the anthracyclinone families. Part 1: Synthesis of bicyclic precursors of 4-demethoxy-7-deoxy-derivatives

A new and versatile strategy to obtain enantiomerically pure bicyclic precursors of compounds belonging to different anthracyclinone families is reported. Completely stereoselective hydrocyanation of (R)-4-(2,5-dimethoxyphenyl)-1-p-tolysulfinyl-2-butanone