1123671-37-3

Basic information

• Product Name: 2-methoxy-4-{[(4-methoxyphenyl)imino]methyl}phenol
• Synonyms: 2-methoxy-4-{[(4-methoxyphenyl)imino]methyl}phenol;2-methoxy-4-{(E)-[(4-methoxyphenyl)imino]methyl}phenol
• CAS NO: 1123671-37-3
• Molecular Formula: C15H15NO3
• Molecular Weight: 257.28
• Mol File: 1123671-37-3.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-methoxy-4-{[(4-methoxyphenyl)imino]methyl}phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methoxy-4-{[(4-methoxyphenyl)imino]methyl}phenol(1123671-37-3)
• EPA Substance Registry System: 2-methoxy-4-{[(4-methoxyphenyl)imino]methyl}phenol(1123671-37-3)

Safety Data

• Hazardous Substances Data: 1123671-37-3(Hazardous Substances Data)

Upstream product

• 110-54-3 hexane 
• 104-94-9 4-methoxy-aniline 
• 121-33-5 vanillin 
• 3391-75-1 2-methoxy-4-((E)-phenylethenyl)phenol 
• 2101-87-3 p-methoxy-phenylazide 

Downstream Products

• 65639-55-6 2-methoxy-4-(7-methoxy-1,1-dioxo-1,2,3,4-tetrahydro-1λ⁶-benzo[1,4]thiazin-3-yl)-phenol 
• 121-34-6 3-methoxy-4-hydroxybenzoic acid 
• 501-58-6 bis(4-methoxyphenyl)diazene 
• 1401204-98-5 C₂₂H₂₂N₂O₄ 
• 58285-79-3 2-methoxy-4-(((4-methoxyphenyl)amino)methyl)phenol 
• 1401205-09-1 C₂₂H₂₂N₂O₃S 

Relevant articles and documents

Iron-Catalyzed Nitrene Transfer Reaction of 4-Hydroxystilbenes with Aryl Azides: Synthesis of Imines via C=C Bond Cleavage

C=C bond breaking to access the C=N bond remains an underdeveloped area. A new protocol for C=C bond cleavage of alkenes under nonoxidative conditions to produce imines via an iron-catalyzed nitrene transfer reaction of 4-hydroxystilbenes with aryl azides is reported. The success of various sequential one-pot reactions reveals that the good compatibility of this method makes it very attractive for synthetic applications. On the basis of experimental observations, a plausible reaction mechanism is also proposed.

Synthesis, characterization and antimicrobial evaluation of some schiff bases and their thiazolidinone products

Six isomeric nitro- and methoxy anilines were condensed with vanillin to obtain Schiff's bases. A new series of 2-(4-hydroxy-3-methoxy phenyl)-1-thiazolidinone derivatives were synthesized by the cyclocondensation of Schiff's bases with mercapto acetic ac

GREEN SYNTHESIS OF ARYL ALDIMINES USING ETHYL LACTATE

The present invention relates to a method for preparing aryl aldimines. In particular, the present invention relates to methods of preparing aryl aldimines that uses environmentally friendly solvent systems.