71128-83-1

Upstream product

• 50-00-0 formaldehyd 
• 104-93-8 p-methylanizole 
• 106-44-5 p-cresol 
• 91-04-3 2,6-bis(hydroxymethyl)-4-methylphenol 
• 7310-95-4 2-Hydroxy-5-methylisophthalaldehyde 
• 74-88-4 methyl iodide 
• 6327-85-1 2,6-bis(hydroxymethyl)-4-methyl-anisole 

Downstream Products

• 7310-95-4 2-Hydroxy-5-methylisophthalaldehyde 
• 6327-85-1 2,6-bis(hydroxymethyl)-4-methyl-anisole 
• 1200527-97-4 C₃₂H₅₄O₃Si₂ 
• 1200528-12-6 meso-2,6-bis(-1-hydroxy-3-trimethylsilylprop-2-ynyl)-4-methyl-anisole 
• 71128-85-3 (3-Hydroxymethyl-2-methoxymethoxy-5-methyl-phenyl)-methanol 
• 71128-84-2 2-Methoxymethoxy-5-methylisophthalaldehyd 
• 110569-85-2 2,6-bis<6-<5-(ethoxycarbonyl)-2-<<5-(2,2-dicyanovinyl)-3-ethyl-4-methylpyrrol-2-yl>methyl>-4-methylpyrrol-3-yl>-hexyl>-4-methylanisole 
• 110569-86-3 2,6-bis<5-<5-(ethoxycarbonyl)-2-<<5-(2,2-dicyanovinyl)-3-ethyl-4-methylpyrrol-2-yl>methyl>-4-methylpyrrol-3-yl>-pentyl>-4-methylanisole 
• 110569-87-4 C₅₀H₆₆N₄O₇ 
• 110589-05-4 C₄₈H₆₆N₄O₃ 
• 110569-84-1 2,6-bis<6-<5-(ethoxycarbonyl)-4-methylpyrrol-3-yl>-1-hexyl>-4-methylanisole 
• 110589-04-3 2,6-bis<5-<5-(ethoxycarbonyl)-4-methylpyrrol-3-yl>-pentyl>-4-methylanisole 
• 680575-43-3 5-[2-methoxy-5-methyl-3-(4-methyl-5-oxo-penta-1,3-dienyl)-phenyl]-2-methyl-penta-2,4-dienal 

Relevant academic research and scientific papers

Serial synthesis of oxa[3.n]cyclophanes and homooxacalix[n]arenes via reductive coupling of arenedialdehydes, and their X-ray structures

A wide range of oxa[3.n]cyclophanes and homooxacalix[n]arenes is prepared from the corresponding arenedialdehyde via reductive homocoupling reaction in a one-pot fashion. Heterocoupling reaction of arenedialdehyde with bis(trimethylsilyloxymethyl)benzene provides a series of macrocyclic ethers including a new type of oxacalixarene, which consists of the moieties of oxa[3.n]cyclophane and homooxacalix[n]arene; m- or p-phenylene, and 5-substituted 2-methoxy-m-phenylene are tethered by CH2 OCH2 linkages. A series of macrocycles are separated with gel permeation chromatography (GPC) and identified with NMR (1H, 13C) and mass (MALDI-TOF) spectra. Their solid-state conformations are elucidated by X-ray crystallographic analyses.

Synthesis of novel benzo-substituted macrocyclic schiff bases containing two triazole rings

(Chemical Equation Presented) A synthesis of a series of novel macrocyclic Schiff bases containing two triazole rings 10a,b, 11a,b, 34-37 in good yields by heating the appropriate bis-amines 1f, 6a,b, 31 with the corresponding bis-aldehydes 2, 9a,b, 29 in

Synthesis of Hydrocarbon-Strapped Porphyrins Containing Quinone and Phenolic Groups

A general synthesis of strapped porphyrins is described and is illustrated for porphyrins bearing quinone and phenol groups in the bridging strap, which is exclusively a polymethylene chain.The NMR and optical spectra of the strapped porphyrins are discussed.