58259-46-4

Upstream product

• 95-01-2 2,4-Dihydroxybenzaldehyde 
• 96089-43-9 2-hydroxy-4-<(carboxymethyl)oxy>benzaldehyde ethyl ester 
• 74-88-4 methyl iodide 

Downstream Products

• 875801-90-4 ethyl 2-(4-[(E)-2-(1,3-dimethyl-5-nitro-2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)ethenyl]-3-methoxyphenyloxy)acetate 
• 51336-33-5 1,2,6-Trimethyl-4-(3-methoxy-4-ethoxycarbonylmethoxyphenyl)-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester 
• 875802-34-9 [4-(2,4-dioxo-1,3-dipropyl-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-3-methoxy-phenoxy]-acetic acid ethyl ester 
• 480994-25-0 ethyl 2-[4-(1,3-dimethyl-2,4-dioxo-2,3,4,5-tetrahydro-1H-pyrrolo[3,2-d]pyrimidin-6-yl)-3-methoxyphenyloxy]acetate 
• 875801-94-8 {3-Methoxy-4-[(E)-2-(5-nitro-2,6-dioxo-1,3-dipropyl-1,2,3,6-tetrahydro-pyrimidin-4-yl)-vinyl]-phenoxy}-acetic acid ethyl ester 

Relevant academic research and scientific papers

Preparation method of 4-hydroxymethyl-3-methoxyphenoxyacetic acid

The invention discloses a preparation method of 4-hydroxymethyl-3-methoxyphenoxyacetic acid, comprising the steps of a) subjecting the start material 2,4-dihydroxybenzaldehyde and halogenated ethyl acetate to nucleophilic substitution reaction under the a

2-arylimidazopyridines intermediates

New 2-arylimidazopyridines of the general formula I STR1 wherein --A=B-- is (a) --CH=N-- or (b) N=CH--, Ar is a phenyl radical, which, in case (a), is substituted by one or two alkynyloxy, cyanomethoxy, carboxymethoxy, and/or alkyloxycarbonylmethoxy group