1394025-13-8

Basic information

• Product Name: C₄₅H₃₃N
• Synonyms: C₄₅H₃₃N
• CAS NO: 1394025-13-8
• Molecular Weight: 587.764
• Mol File: 1394025-13-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₄₅H₃₃N(CAS DataBase Reference)
• NIST Chemistry Reference: C₄₅H₃₃N(1394025-13-8)
• EPA Substance Registry System: C₄₅H₃₃N(1394025-13-8)

Safety Data

• Hazardous Substances Data: 1394025-13-8(Hazardous Substances Data)

Upstream product

• 626-05-1 2,6-Dibromopyridine 
• 536-74-3 phenylacetylene 
• 83965-72-4 2,6-bis(2-phenylethynyl)pyridine 
• 100-58-3 phenylmagnesium bromide 
• 1607-57-4 Triphenylvinyl bromide 
• 219488-97-8 4,4,5,5-tetramethyl-2-(1,2,2-triphenylvinyl)-1,3,2-dioxaborolane 

Relevant articles and documents

Luminogens for Aggregation-Induced Emission via Titanium-Mediated Double Nucleophilic Addition to 2,5-Dialkynylpyridines: Formation and Transformation of the Emitting Aggregates

New luminogens for aggregation-induced emission (AIE), which are characterized by a branched cross-conjugated 2,6-bis(1,2,2-triarylvinyl)pyridine motif, have been synthesized exploiting the one-pot Ti-mediated tetraarylation of 2,6-bis(arylethynyl)pyridin

Pyridine-cored V-shaped π-conjugated oligomers: Synthesis and optical properties

A new series of V-shaped pyridine-cored π-conjugated oligomers are synthesized utilizing two-fold Heck/Suzuki coupling reactions. Optical properties of these compounds (λmax=390-449 nm, Φfl=79-5%, in solutions) are discussed. They are shown to be thermally stable and soluble in common organic solvents. Stilbenoid oligomers exhibited much higher fluorescence quantum yields than tri- and tetra-phenylethylene substituted oligomers in solutions.