36294-21-0

Usage

InChI:InChI=1/C10H8O.K/c11-10-6-5-8-3-1-2-4-9(8)7-10;/h1-7,11H;/q;+1/p-1

Upstream product

• 865-33-8 potassium methanolate 
• 135-19-3 β-naphthol 

Downstream Products

• 10484-56-7 2-butoxynaphthalene 
• 16712-64-4 6-Hydroxy-2-naphthoic acid 
• 92-70-6 3-Hydroxy-2-naphthoic acid 
• 865-33-8 potassium methanolate 
• 135-19-3 β-naphthol 
• 29114-24-7 benzylidene-1,1'-bis(2-naphthol) 
• 36441-31-3 1-benzyl-2-naphthol 
• 6036-14-2 ethyl (naphthalen-2-yloxy)acetate 
• 613-62-7 2-benzyloxynaphthalene 
• 2283-08-1 2-hydroxy-1-naphthalenecarboxylic acid 
• 602-09-5 1,1'-bi-2-naphthol 
• 15330-39-9 7a,14c-dihydronaphtho<2,1-b>naphtho<2',1':5,6>furo<3,2-d>furan 
• 133523-54-3 1-(2-hydroxy-1,2-dihydronaphtho<2,1-b>furan-1-yl)-2-naphthol 
• 4352-63-0 1H-naphtho[2,1-b]furan-2-one 

Relevant academic research and scientific papers

Kinetics and mechanism of reaction of 1-chloro-2,4-dinitrobenzene with potassium phenoxide, 1-naphthoxide and 2-naphthoxide in methanol

In the title reaction at different temperatures (30-45 deg C) the rates have been measured as a function of free .A linear relationship is found between the observed second order rate coefficient and the ratio /.This has been attributed to concurrent and consecutive methanolysis by methoxide ions arising from the possible proton exchange between methanol and phenoxide ion.The thermodynamic parameters of activation of the reaction of 1-chloro-2,4-dinitrobenzene with aryl oxides and methoxide anions have been calculated.From the kinetic results it is possible to calculate the equilibrium constant of the reaction: CH3OH + ArO(-) CH3O(-) + ArOH