1190880-27-3

Basic information

• Product Name: 1,1'-[(4-chlorophenyl)methanediyl]bis(2,4,5-trimethoxybenzene)
• Synonyms: 1,1'-[(4-chlorophenyl)methanediyl]bis(2,4,5-trimethoxybenzene)
• CAS NO: 1190880-27-3
• Molecular Weight: 458.939
• Mol File: 1190880-27-3.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1,1'-[(4-chlorophenyl)methanediyl]bis(2,4,5-trimethoxybenzene)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1'-[(4-chlorophenyl)methanediyl]bis(2,4,5-trimethoxybenzene)(1190880-27-3)
• EPA Substance Registry System: 1,1'-[(4-chlorophenyl)methanediyl]bis(2,4,5-trimethoxybenzene)(1190880-27-3)

Safety Data

• Hazardous Substances Data: 1190880-27-3(Hazardous Substances Data)

Upstream product

• 135-77-3 1,2,4-trimethoxy-benzene 
• 104-88-1 4-chlorobenzaldehyde 
• 3157-65-1 N-(p-chlorobenzylidene)-p-toluenesulfonamide 
• 1190880-19-3 C₂₃H₂₃ClO₅S 

Relevant articles and documents

Niobium Pentachloride Mediated (Hetero)aromatic Aldehyde Friedel-Crafts Hydroxyalkylation with Arenes: An Efficient Strategy to Synthesize Triarylmethanes

Niobium pentachloride is an efficient and useful Lewis acid to conduct Friedel-Crafts hydroxyalkylation between arenes and (hetero)aromatic aldehydes, to generate triarylmethanes. This practical methodology offers several advantages, such as short reaction time, mild experimental conditions, and excellent yields.

A new practical synthesis of triaryl and trisindolylmethanes under solvent-free reaction conditions

An efficient and practical synthesis of triaryl and trisindolylmethanes is reported via the bisarylation of aryl aldehydes with activated arenes. The new method features mild solvent-free reaction conditions, in most cases nearly stoichiometric reagent ra

Regioselective arylations of α-amido sulfones with electron-rich arenes through friedel-crafts alkylations catalyzed by ferric chloride hexahydrate: Synthesis of unsymmetrical and bis-symmetrical triarylmethanes

Ferric chloride hexahydrate is a highly efficient catalyst for the regioselective arylation of α-amido sulfones. The products undergo further Friedel-Crafts alkylations with heteroaromatic or electron-rich arenes to afford unsymmetrical or bis-symmetrical