71573-24-5

Upstream product

• 36383-33-2 4-nitro-1,2-benzenediol diacetate 
• 3316-09-4 1,2-dihydroxy-4-nitrobenzene 

Downstream Products

• 159788-47-3 Fumarsaeuremono-3,4-diacetoxyanilid 
• 74332-02-8 4-N-acetylamino-1,2-benzenediol diacetate 
• 263745-42-2 N-(3,4-diacetoxyphenyl)-formamide 
• 263745-43-3 3,4-diacetoxybenzoisocyanide 
• 1427449-99-7 1-(3,4-diacetoxylphenyl)-5-(fluoromethyl)pyrrolidin-2-one 
• 1427450-14-3 N-(3,4-diacetoxyphenyl)-4-pentenamide 
• 1428333-03-2 C₂₀H₁₇N₃O₈ 
• 76149-14-9 3,4-dihydroxy-iodobenzene 
• 37519-14-5 3-Hydroxyacetaminophen 
• 159788-32-6 3,4-Diacetoxycarbanilidsaeure-norborn-5-en-2,3-dicarboximidester 

Relevant academic research and scientific papers

Thiazolocatechol: Electron-Withdrawing Catechol Anchoring Group for Dye-Sensitized Solar Cells

Anchoring groups adopting a five-membered bidentate chelating are attractive to realize high power conversion efficiency (η) and long-term durability in dye-sensitized solar cells (DSSCs). In this regard, we chose catechol as an anchoring group that can a

Efficient synthesis of 5,6-dihydroxyindole dimers, key eumelanin building blocks, by a unified o-ethynylaniline-based strategy for the construction of 2-linked biindolyl scaffolds

(Chemical Equation Presented) A unified convenient strategy for the synthesis of 5,6-dihydroxyindole-derived 2,7′-, 2,2′-, and 2,3′-biindolyls is reported, which is based on proper manipulation of key o-ethynylaniline precursors. By the same methodology 5

Towards the synthesis of aminodibenzo[b,e][1,4]dioxin derivatives via cationic ruthenium complexes

Double nucleophilic aromatic substitution reactions between N-substituted (η6-1,2-dichlorobenzene)RuCp+ salts and substituted 1,2-benzenediols have been carried out under mild conditions to prepare N-substituted (η6-dibenzo[b,e][1,4]dioxin)ruthenium(II) complexes. The dibenzodioxin ligands were subsequently liberated by photolysis, with radiation from a sunlamp or from a medium pressure Hg lamp (300 nm).

Synthesis and antibacterial activity of new ureido and dicarbonic acid diamido derivaties of acylpenicillines with and without catechol substituents

New ureido, oxamoyl, fumaramoyl and terephthalamoyl derivatives of ampicillin or amoxicillin were synthesized by reaction of acylpenicillines with o-dihydroxy- or odiacyloxy substituents containing aromatic amines bound over CO- or dicarboxylic groups. Co