115967-47-0

Basic information

• Product Name: phenyl 3,4,5-trimethoxybenzoate
• Synonyms: phenyl 3,4,5-trimethoxybenzoate
• CAS NO: 115967-47-0
• Molecular Formula: C₁₆H₁₆O₅
• Molecular Weight: 288.29524
• Mol File: 115967-47-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: phenyl 3,4,5-trimethoxybenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 3,4,5-trimethoxybenzoate(115967-47-0)
• EPA Substance Registry System: phenyl 3,4,5-trimethoxybenzoate(115967-47-0)

Safety Data

• Hazardous Substances Data: 115967-47-0(Hazardous Substances Data)

Upstream product

• 4521-61-3 3,4,5-Trimethoxybenzoyl chloride 
• 98-80-6 phenylboronic acid 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 108-95-2 phenol 
• 42543-45-3 3,4,5-trimethoxybenzoyl azide 
• 3291-03-0 3,4,5-trimethoxybenzohydrazide 

Downstream Products

• 99265-10-8 1-phenyl-3-(3,4,5-trimethoxyphenyl)-1,3-propanedione 

Relevant articles and documents

Transition-Metal-Free Poly(thiazolium) Iodide/1,8-Diazabicyclo[5.4.0]undec-7-ene/Phenazine-Catalyzed Esterification of Aldehydes with Alcohols

Poly(3,4-dimethyl-5-vinylthiazolium) iodide was used as a polymer precatalyst in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) and phenazine for the oxidative esterification of aldehydes with alcohols. Selective functionalization of OH groups was achieved in the presence of NH2 groups. The poly(thiazolium) iodide/DBU/phenazine system exhibited excellent catalytic activity and could be reused five times without loss of activity.

N-heterocyclic carbene-catalyzed aerobic oxidative direct esterification of aldehydes with organoboronic acids

A simple procedure affording benzoates through a NHC-catalyzed aerobic oxidative esterification of aldehydes with organoboronic acids has been disclosed. This process allows access to a wide variety of aromatic esters in good to excellent yields under simple, efficient, and sustainable reaction conditions (see scheme).