104575-17-9

Upstream product

• 117942-41-3 4-[(2-methoxyethoxy)methoxy]benzaldehyde 
• 3970-21-6 2-Methoxyethoxymethyl chloride 
• 767-00-0 4-cyanophenol 

Downstream Products

• 104575-23-7 (E)-1-{4-[2-(diethylamino)ethoxy]phenyl}-1-(4-hydroxyphenyl)-2-nitro-2-phenylethene 
• 104575-14-6 (Z)-1-<4-<2-(diethylamino)ethoxy>phenyl>-1-(4-hydroxyphenyl)-2-nitro-2-phenylethene 
• 104575-10-2 (E)-1-{4-[2-(diethylamino)ethoxy]phenyl}-1-(4-hydroxyphenyl)-2-bromo-2-phenylethene 
• 104575-11-3 (Z)-1-<4-<2-(diethylamino)ethoxy>phenyl>-1-(4-hydroxyphenyl)-2-bromo-2-phenylethene 
• 104575-18-0 4-<2-(diethylamino)ethoxy>-4'-<(methoxyethoxy)methyloxy>benzophenone 
• 104575-19-1 1-<4-<2-(diethylamino)ethoxy>phenyl>-1-<4-<(methoxethoxy)methyloxy>phenyl>-2-phenylethene hydrochloride 
• 104575-20-4 Diethyl-[2-(4-{(Z)-1-[4-(2-methoxy-ethoxymethoxy)-phenyl]-2-nitro-2-phenyl-vinyl}-phenoxy)-ethyl]-amine 

Relevant academic research and scientific papers

Binding interactions between 3-aryl-1,2,4-oxadiazol-5-ones and a trisimidazoline base

The use of 1,2,4-oxadiazol-5-ones, a recently developed class of bioisosteric replacements for carboxylic acids in medicinal chemistry, as binding ligands in supramolecular complexes is reported and has been exemplified by the formation of non-covalent co

A new one pot method for the conversion of aldehydes into nitriles using hydroxyamine and phthalic anhydride

The aryl and alkyl aldehydes were readily converted to give the corresponding nitrites in good yields using hydroxyamine and phthalic anhydride as reagents in one pot.