82997-81-7

Upstream product

• 82063-02-3 3,3'-(2,5-dimethoxy-p-phenylene)bispropenoic acid 
• 7310-97-6 2,5-dimethoxyterephthalaldehyde 
• 114558-97-3 1,1'-(2,5-dimethoxy-p-xylylene)-bis-hexamethylenetetraminium; dichloride 
• 3752-97-4 1,4-bis(chloromethyl)-2,5-dimethoxybenzene 
• 13949-89-8 tetraethyl 1,4-diethyl-2,5-dimethoxybenzene-ω,ω,ω',ω'-tetracarboxylate 
• 64-17-5 ethanol 
• 40995-85-5 3,3'-(2,5-dimethoxy-p-phenylene)-di-propionic acid 

Downstream Products

• 5628-27-3 3,3'-(2,5-Dimethoxy-1,4-phenylen)di-1-propanol 
• 82997-85-1 Acetic acid 3-[4-(3-acetoxy-propyl)-2,5-bis-methoxymethoxy-phenyl]-propyl ester 
• 82997-82-8 2,5-bis(3-acetoxypropyl)-1,4-dimethoxybenzene 
• 22501-42-4 Acetic acid 3-[4-(3-acetoxy-propyl)-2,5-dihydroxy-phenyl]-propyl ester 
• 76942-15-9 2,5-bis(3-hydroxypropyl)-1,4-bis(methoxymethoxy)benzene 
• 13949-80-9 2,5-bis(3-acetoxypropyl)-1,4-benzoquinone 

Relevant academic research and scientific papers

Synthesis of Bipyridyl-, Viologen-, and Quinone-bridged Porphyrins

Mesoporphyrin-II has been bridged by several 2,2'-hydroxymethyl-substituted 4,4'-bipyridine compounds.N-Methylation of the bipyridine bridge groups yielded viologen-bridged porphyrins which have unusual aggregation and fluorescence properties.An improved route to quinone-bridged porphyrins is also reported.

Quinone-capped Porphyrins: Synthesis and some Chemical Properties

The 2,5-bis(hydroxyethyl) and 2,5-bis(hydroxypropyl) derivatives of hydroquinone bis(methoxymethyl) ether have been synthesised and used to 'cap' mesoporphyrin-II.Deprotection, oxidation, and metallation gave the title compounds.Several anomalous reactivi