62397-61-9

Basic information

• Product Name: 2,5-Dimethoxybenzenepropanoic acid methyl ester
• Synonyms: 2,5-Dimethoxybenzenepropanoic acid methyl ester
• CAS NO: 62397-61-9
• Molecular Formula: C₁₂H₁₆O₄
• Molecular Weight: 224.253
• Mol File: 62397-61-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 311.5°Cat760mmHg
• Flash Point: 134.3°C
• Appearance: /
• Density: 1.084g/cm³
• Vapor Pressure: 0.000561mmHg at 25°C
• Refractive Index: 1.494
• CAS DataBase Reference: 2,5-Dimethoxybenzenepropanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Dimethoxybenzenepropanoic acid methyl ester(62397-61-9)
• EPA Substance Registry System: 2,5-Dimethoxybenzenepropanoic acid methyl ester(62397-61-9)

Safety Data

• Hazardous Substances Data: 62397-61-9(Hazardous Substances Data)

Usage

General Description

2,5-Dimethoxybenzenepropanoic acid methyl ester, also known as DMBP, is a chemical compound with the molecular formula C12H16O5. It is an ester derivative of 2,5-dimethoxybenzenepropanoic acid and is commonly used in organic synthesis and pharmaceutical research. DMBP is a colorless to pale yellow liquid with a sweet, floral odor and is soluble in organic solvents. It is often utilized as a precursor in the synthesis of various psychoactive compounds, such as designer drugs and hallucinogens. The compound is also used as a building block for the production of pharmaceuticals and agrochemicals due to its versatile reactivity and functional groups. Additionally, it is under regulatory scrutiny due to its potential for misuse and abuse.

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

Relevant articles and documents

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.

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