907959-18-6

Basic information

• Product Name: 1,3,5-tris[(4-methoxyphenyl)methyl]benzene
• Synonyms: 1,3,5-tris[(4-methoxyphenyl)methyl]benzene
• CAS NO: 907959-18-6
• Molecular Weight: 438.566
• Mol File: 907959-18-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3,5-tris[(4-methoxyphenyl)methyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-tris[(4-methoxyphenyl)methyl]benzene(907959-18-6)
• EPA Substance Registry System: 1,3,5-tris[(4-methoxyphenyl)methyl]benzene(907959-18-6)

Safety Data

• Hazardous Substances Data: 907959-18-6(Hazardous Substances Data)

Upstream product

• 108-70-3 1,3,5-trichlorobenzene 
• 824-94-2 p-methoxybenzyl chloride 
• 13540-76-6 3-(4-methoxyphenyl)prop-1-yne 
• 2749-94-2 1-methoxy-4-(prop-1-yn-1-yl)benzene 
• 4180-23-8 E-1-(4'-methoxyphenyl)prop-1-ene 
• 73172-23-3 benzene-1,3,5-triyltris[(4-methoxyphenyl)methanone] 
• 1415037-87-4 C₁₀H₉O₃^(1-)*K⁽¹⁺⁾ 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Downstream Products

• 1415037-89-6 1,3,5-tris[(4-cyanatophenyl)methyl]benzene 
• 149228-33-1 1,3,5-tris[(4-hydroxyphenyl)methyl]benzene 

Relevant articles and documents

Nickel-Catalyzed Reductive Cross-Coupling of Benzyl Chlorides with Aryl Chlorides/Fluorides: A One-Pot Synthesis of Diarylmethanes

The first nickel-catalyzed, magnesium-mediated reductive cross-coupling between benzyl chlorides and aryl chlorides or fluorides is reported. A variety of diarylmethanes can be prepared in good to excellent yields in a one-pot manner using easy-to-access mixed PPh3/NHC Ni(II) complexes of Ni(PPh3)(NHC)Br2 (NHC = 1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene, IPr, 1a; 1,3-di-tert-butylimidazol-2-ylidene, ItBu, 1b) as catalyst precursors. Activation of polychloroarenes or chemoselective cross-coupling based on the difference in catalytic activity between 1a and 1b is used to construct oligo-diarylmethane motifs.

Polycyanurate networks with enhanced segmental flexibility and outstanding thermochemical stability

The synthesis and physical properties of cyanurate networks formed from two new tricyanate monomers, 1,3,5-tris[(4-cyanatophenylmethyl]benzene and 3,5-bis[(4-cyanatophenylmethyl)]phenylcyanate, are reported and compared to those of 1,1,1-tris[(4-cyanatoph