75867-42-4

Basic information

• Product Name: Silane, ([1,1'-biphenyl]-4-ylethynyl)trimethyl-
• CAS NO: 75867-42-4
• Molecular Formula: C17H18Si
• Molecular Weight: 250.415
• Mol File: 75867-42-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Silane, ([1,1'-biphenyl]-4-ylethynyl)trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Silane, ([1,1'-biphenyl]-4-ylethynyl)trimethyl-(75867-42-4)
• EPA Substance Registry System: Silane, ([1,1'-biphenyl]-4-ylethynyl)trimethyl-(75867-42-4)

Safety Data

• Hazardous Substances Data: 75867-42-4(Hazardous Substances Data)

Upstream product

• 92-66-0 4-bromo-1,1'-biphenyl 
• 78389-87-4 ((trimethylsilyl)ethynyl)zinc(II) chloride 

Downstream Products

• 1557159-22-4 1-([1,1'-biphenyl]-4-ylethynyl)-1,2-benziodoxol-3(1H)-one 
• 2920-38-9 4-cyano-1,1'-biphenyl 
• 710984-37-5 1-[1,1'-biphenyl]-4-yl-2-[(4-methylphenyl)sulfonyl]-1-ethanone 
• 41024-57-1 1-([1,1’-biphenyl]-4-yl)-2-(phenylsulfonyl)ethanone 
• 1595282-13-5 (Z)-(2-([1,1'-biphenyl]-4-yl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)trimethylsilane 
• 1595281-97-2 (Z)-(2-([1,1'-biphenyl]-4-yl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)vinyl)trimethylsilane 
• 1557159-43-9 2-([1,1'-biphenyl]-4-ylethynyl)-2,3-dihydro-1H-indene 
• 29079-15-0 1,4-di[(1,1′-biphenyl)-4-yl]buta-1,3-diyne 
• 56316-86-0 2,5-bis(biphenyl-4-yl)thiophene 
• 383191-40-0 1-(2-biphenyl-4-ylethynyl-phenyl)-3-{4-[3-(2-biphenyl-4-ylethynyl-phenyl)-1-tert-butyl-1-hydroxy-prop-2-ynyl]-phenyl}-4,4-dimethyl-pent-1-yn-3-ol 
• 383191-44-4 C₄₈H₄₂(C₆H₄)2 
• 383191-53-5 (2-biphenyl-4-ylethynyl-phenylethynyl)-trimethyl-silane 
• 383191-39-7 4-((2-ethynylphenyl)ethynyl)-1,1'-biphenyl 

Relevant articles and documents

Synthesis of polyphenylene derivatives by thermolysis of enediynes and dialkynylaromatic monomers

Described are the syntheses of substituted enediynes and dialkynylaromatics using Pd- or Pd/Cu-catalyzed cross coupling procedures. The products were then thermalized to afford the corresponding poly(p- phenylene)s, poly(1,4-naphthalene)s, poly(benzo[c]thiophene)s, and poly(dibenzothiophene)s. Fifteen examples are provided that show the scope of the polymerization process based upon substituent patterns and cyclization moieties. The superb thermal resiliency of the newly derived polymers is demonstrated using thermogravimetric analysis. The polymer structure was generally confirmed using IR data correlations to small molecules that resembled the polymers' repeat unit structure. Radical trapping of dimeric intermediates, that were analyzed by GCMS, further substantiated the proposed mechanistic route. The step-growth polymerization pattern was determined by monitoring the degree of monomer consumption versus the polymer molecular weight.