6178-45-6

Basic information

• Product Name: propyl 3,4,5-trimethoxybenzoate
• Synonyms: propyl 3,4,5-trimethoxybenzoate;3,4,5-Trimethoxybenzoic acid propyl ester;Einecs 228-225-1
• CAS NO: 6178-45-6
• Molecular Formula: C₁₃H₁₈O₅
• Molecular Weight: 254.27902
• EINECS: 228-225-1
• Mol File: 6178-45-6.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 308.9°C at 760 mmHg
• Flash Point: 131.1°C
• Appearance: /
• Density: 1.094g/cm³
• Vapor Pressure: 0.000663mmHg at 25°C
• Refractive Index: 1.491
• CAS DataBase Reference: propyl 3,4,5-trimethoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: propyl 3,4,5-trimethoxybenzoate(6178-45-6)
• EPA Substance Registry System: propyl 3,4,5-trimethoxybenzoate(6178-45-6)

Safety Data

• Hazardous Substances Data: 6178-45-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H18O5/c1-5-6-18-13(14)9-7-10(15-2)12(17-4)11(8-9)16-3/h7-8H,5-6H2,1-4H3

Upstream product

• 71-23-8 propan-1-ol 
• 118-41-2 Eudesmic acid 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 121-79-9 Propyl gallate 
• 74-88-4 methyl iodide 

Downstream Products

• 3840-31-1 (3,4,5-trimethoxyphenyl)methanol 

Relevant articles and documents

N-Heterocyclic Carbene-Mediated Oxidative Electrosynthesis of Esters in a Microflow Cell

An efficient N-heterocyclic carbene (NHC)-mediated oxidative esterification of aldehydes has been achieved in an undivided microfluidic electrolysis cell at ambient temperature. Productivities of up to 4.3 g h-1 in a single pass are demonstrated, with excellent yields and conversions for 19 examples presented. Notably, the oxidative acylation reactions were shown to proceed with a 1:1 stoichiometry of aldehyde and alcohol (for primary alcohols), with remarkably short residence times in the electrolysis cell (13 s), and without added electrolyte. (Chemical Equation Presented).