10373-41-8

Upstream product

• 108-73-6 3,5-dihydroxyphenol 
• 64-17-5 ethanol 
• 28334-98-7 Phloroglucinmonoethylether 
• 83-30-7 acide 2,4,6-trihydroxybenzoique 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 26207-59-0 2,4-diethoxy-6-hydroxyacetophenone 
• 857564-15-9 1-(2,6-diethoxy-4-hydroxy-phenyl)-ethanone 
• 2437-88-9 1,3,5-triethoxy benzene 
• 77670-47-4 3'',5''-diethoxyphenyl 4',5,7-trimethoxyflavone-3'-ylacetate 
• 90875-96-0 2-Chloro-3,5-diethoxy-phenol 
• 75552-20-4 4-chloro-3,5-diethoxyphenol 
• 76238-99-8 4,6-diethoxysalicylaldehyde 
• 93810-16-3 4-Hydroxy-1-<3.5-diaethoxy-phenoxy>-cyclohexan-carbonsaeure-(1) 
• 93810-07-2 1-<3,5-Diaethoxy-phenoxy>-cyclohexan-carbonsaeure-(1) 
• 3186-92-3 2-Hydroxy-4,6-diaethoxy-benzoesaeure 
• 236747-80-1 3,5-diethoxyphenyl trifluoromethanesulfonate 
• 38730-43-7 2,4-dichloro-3,5-diethoxyphenol 
• 38730-56-2 2-Aminomethyl-4,6-dichloro-3,5-diethoxy-phenol; hydrochloride 
• 870652-03-2 (4-bromophenyl)-(3,5-diethoxyphenoxy)-acetic acid methyl ester 

Relevant academic research and scientific papers

NOVEL CYLOPENTA[B]BENZOFURAN DERIVATIVES AND THE UTILIZATION THEREOF

The invention relates to novel cyclopenta[b]benzofuran derivatives, to a method for the production thereof and to their utilization for the production of medicaments, especially for the prophylaxis and/or therapy of acute or chronic diseases which are cha

SYNTHESIS OF PHLOROGLUCINOL TRIALKYL ETHERS

The alkylation of phloroglucinol dialkyl ethers with alcohols or alkyl halides leads, depending on the reaction conditions, either to products of O- or C- alkylation, or to C,O-alkylation products.Reaction conditions were found which enable us to obtain pure phloroglucinol trialkyl ethers.A convenient preparative method for the synthesis of phloroglucinol trialkyl ethers consists in the alkylation of phloroglucinol dialkyl ethers in a two-phase system in presence of phase-transfer catalysts.