62256-40-0

Basic information

• Product Name: 2-(2-methoxyphenoxy)benzaldehyde
• Synonyms: 2-(2-methoxyphenoxy)benzaldehyde
• CAS NO: 62256-40-0
• Molecular Formula: C₁₄H₁₂O₃
• Molecular Weight: 228.24328
• Mol File: 62256-40-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-methoxyphenoxy)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-methoxyphenoxy)benzaldehyde(62256-40-0)
• EPA Substance Registry System: 2-(2-methoxyphenoxy)benzaldehyde(62256-40-0)

Safety Data

• Hazardous Substances Data: 62256-40-0(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 72, p. 4797, 1950 DOI: 10.1021/ja01166a128

Upstream product

• 446-52-6 2-Fluorobenzaldehyde 
• 90-05-1 2-methoxy-phenol 
• 578-57-4 2-bromoanisole 

Downstream Products

• 6702-58-5 4-methoxy-9H-xanthen-9-one 
• 912461-47-3 tert-butyl 9-[2-(2-methoxyphenoxy)benzyl]-3,9-diazaspiro[5.5]undecane-3-carboxylate 
• 1179356-21-8 3-[2-(2-methoxyphenoxy)benzyl]-9-(pyridin-4-ylcarbonyl)-3,9-diazaspiro[5.5]undecane trifluoroacetate 
• 1179356-24-1 3-[2-(2-methoxyphenoxy)benzyl]-9-(pyrimidin-4-ylcarbonyl)-3,9-diazaspiro[5.5]undecane trifluoroacetate 
• 851326-47-1 3-(4-chlorobenzoyl)-9-[2-(2-methoxyphenoxy)benzyl]-3,9-diazaspiro[5.5]undecane trifluoroacetate 
• 136093-58-8 methyl 2-(2-hydroxyphenoxy)-α-bromobenzeneacetate 
• 136093-57-7 2-(2-hydroxyphenoxy)-α-bromobenzeneacetic acid 
• 136093-56-6 2-(2-methoxyphenoxy)-α-hydroxybenzeneacetic acid 
• 21905-73-7 2-carboxy-2'-methoxydiphenyl ether 

Relevant articles and documents

Metal-free oxidative coupling: Xanthone formation via direct annulation of 2-aryloxybenzaldehyde using tetrabutylammonium bromide as a promoter in aqueous medium

A metal-free intramolecular annulation of 2-aryloxybenzaldehydes to xanthones is disclosed, which proceeds through the direct oxidative coupling of an aldehyde C-H bond and aromatic C-H bonds using tetrabutylammonium bromide (TBAB) as a promoter in aqueous medium. This strategy works smoothly in the presence of both electron-donating and electron-withdrawing groups, and displays good tolerance towards catalytically reactive substituents, thus promising further functionalizations of xanthone products.