92446-10-1

Basic information

• Product Name: Methanaminium, N-[[[3-(4-hydroxy-3-methoxyphenyl)-1-oxo-2-propenyl]oxy]methylene]-N- methyl-, chloride
• CAS NO: 92446-10-1
• Molecular Formula: C13H16NO4.Cl
• Molecular Weight: 285.727
• Mol File: 92446-10-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Methanaminium, N-[[[3-(4-hydroxy-3-methoxyphenyl)-1-oxo-2-propenyl]oxy]methylene]-N- methyl-, chloride(CAS DataBase Reference)
• NIST Chemistry Reference: Methanaminium, N-[[[3-(4-hydroxy-3-methoxyphenyl)-1-oxo-2-propenyl]oxy]methylene]-N- methyl-, chloride(92446-10-1)
• EPA Substance Registry System: Methanaminium, N-[[[3-(4-hydroxy-3-methoxyphenyl)-1-oxo-2-propenyl]oxy]methylene]-N- methyl-, chloride(92446-10-1)

Safety Data

• Hazardous Substances Data: 92446-10-1(Hazardous Substances Data)

Upstream product

• 1135-24-6 3-(4-hydroxy-3-methoxyphenyl)acrylic acid 
• 68-12-2 N,N-dimethyl-formamide 
• 1135-24-6 (E)-3-(4-hydroxy-3-methoxyphenyl)acrylic acid 
• 3724-43-4 Vilsmeier reagent 

Downstream Products

• 113985-17-4 N-(pyridyl-2 methyl)(hydroxy-4 methoxy-3 phenyl)-3 propene-2 amide 
• 68-12-2 N,N-dimethyl-formamide 
• 56254-02-5 (E)-3-(4-Hydroxy-3-methoxy-phenyl)-thioacrylic acid S-phenyl ester 
• 113985-19-6 N-(phenyl-1 ethyl)(hydroxy-4 methoxy-3 phenyl)-3 propene-2 amide 
• 56254-02-5 -3 thiopropene-2 oate de S-phenyle 
• 458-35-5 coniferal alcohol 
• 458-36-6 trans-coniferyl aldehyde 
• 96014-22-1 (E)-N-(2-(1H-indol-3-yl)ethyl)-3-(4-hydroxy-3-methoxyphenyl)acrylamide 
• 113985-18-5 N-<(pyridyl-2)-2 ethyl>(hydroxy-4 methoxy-3 phenyl)-3 propene-2 amide 
• 2309-07-1 Methyl ferulate 

Relevant articles and documents

Synthesis and evaluation of a novel series of pseudo-cinnamic derivatives as antituberculosis agents

In an effort to develop potent new antituberculous drugs effective against Mycobacterium tuberculosis, we have prepared series of cinnamic derivatives (thioesters and amides) with 4-hydroxy and 4-alkoxy groups and investigated the in vitro activities of these compounds. Among them some displayed a good in vitro antibacterial activity, such as (E)-N-(2-acetamidoethyl)-3-{4-[(E)-3,7-dimethylocta-2,6-dienyloxy]phenyl}acrylamide 4b that showed a minimum inhibitory concentration of 0.1 μg/mL (0.26 μM) against M. tuberculosis H37Rv.

NOUVELLE SYNTHESE DE PRECURSEURS PHENOLIQUES DES LIGNINES UTILISANT LES SELS D'IMINIUM DES ACIDES p-HYDROXY CINNAMIQUES

4-Hydroxy cinnamic esters, thiolesters, aldehydes and alcohols, or related compounds, implied in the biosynthesis of lignins are easily synthesized in good yields from iminium salts of coumaric 1a, ferulic 1b and sinapic 1c acids.No prior protection of the phenol group is needed in this method.