852042-91-2

Basic information

• Product Name: 9,9-dihexyl-2-(2'-phenyl-1-ethynyl)fluorene
• Synonyms: 9,9-dihexyl-2-(2'-phenyl-1-ethynyl)fluorene
• CAS NO: 852042-91-2
• Molecular Weight: 434.665
• Mol File: 852042-91-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 9,9-dihexyl-2-(2'-phenyl-1-ethynyl)fluorene(CAS DataBase Reference)
• NIST Chemistry Reference: 9,9-dihexyl-2-(2'-phenyl-1-ethynyl)fluorene(852042-91-2)
• EPA Substance Registry System: 9,9-dihexyl-2-(2'-phenyl-1-ethynyl)fluorene(852042-91-2)

Safety Data

• Hazardous Substances Data: 852042-91-2(Hazardous Substances Data)

Upstream product

• 123863-97-8 9,9-dihexyl-9H-fluorene 
• 536-74-3 phenylacetylene 
• 226070-05-9 2-bromo-9,9-dihexyl-9H-fluorene 
• 319906-42-8 2-iodo-9,9-bis(n-hexyl)fluorene 

Downstream Products

• 869565-43-5 1-(9,9-dihexyl-2-fluorenyl)-2-phenyl-1,2-ethanedione 
• 869565-47-9 1,4-bis(chloromethyl)-2-phenyl-3-(9,9-dihexylfluoren-2-yl)benzene 
• 869565-46-8 1,4-bis(hydroxymethyl)-2-phenyl-3-(9,9-dihexylfluoren-2-yl)benzene 
• 869565-45-7 diethyl 2-phenyl-3-(9,9-dihexylfluoren-2-yl)terephthalate 
• 869565-44-6 diethyl 4-(9,9-dihexyl-2-fluorenyl)-2-oxo-5-phenyl-3,5-cyclopentadiene-1,3-dicarboxylate 
• 910480-98-7 C₅₃H₅₈ 
• 852042-95-6 C₆₁H₅₈ 

Relevant articles and documents

Selective oxidative cyclization by FeCl3 in the construction of 10H-indeno[1,2-b]triphenylene skeletons in polycyclic aromatic hydrocarbons

A novel family of polycyclic aromatic hydrocarbons of various shapes based on the 10H-indeno[1,2-b]-triphenylene skeleton has been synthesized via a reaction sequence of Diels-Alder reaction, decarbonylation, followed by an oxidative cyclization. In parti

Novel poly(2,3-diphenyl-1,4-phenylenevinylene) derivatives containing long branched alkoxy And fluorenyl substituents: Synthesis, characterization, and their applications for polymer light-emitting diodes

Two series of poly(2,3-diphenyl-1,4-phenylenevinylene) (DP-PPV) derivatives containing long branched alkoxy chains or fluorenyl substituents were synthesized. The branched alkoxy groups were introduced to enhance the solubility for spin-coating processes.