103021-71-2

Basic information

• Product Name: 3-chloro-9-phenylfluoren-9-ol
• Synonyms: 3-chloro-9-phenylfluoren-9-ol
• CAS NO: 103021-71-2
• Molecular Weight: 292.765
• Mol File: 103021-71-2.mol

Chemical Properties

• CAS DataBase Reference: 3-chloro-9-phenylfluoren-9-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-chloro-9-phenylfluoren-9-ol(103021-71-2)
• EPA Substance Registry System: 3-chloro-9-phenylfluoren-9-ol(103021-71-2)

Safety Data

• Hazardous Substances Data: 103021-71-2(Hazardous Substances Data)

Upstream product

• 42840-02-8 2-(Toluene-4-sulfonylamino)-benzoyl chloride 
• 108-86-1 bromobenzene 
• 7254-06-0 3-chloro-fluoren-9-one 
• 100-58-3 phenylmagnesium bromide 
• 108-90-7 chlorobenzene 
• 2894-51-1 2-amino-4'-chlorobenzophenone 
• 109394-21-0 3,9-Dichlor-9-phenylfluoren 
• 101868-37-5 2-amino-4'-chlorotriphenylmethanol 

Relevant articles and documents

Nitrogen heterocyclic ring-containing organic electroluminescent compound as well as preparation method and application thereof

The invention provides a nitrogen heterocyclic ring-containing organic electroluminescent compound, as well as a preparation method and application thereof. The nitrogen heterocyclic ring-containing organic electroluminescent compound has a structure as s

Competition in Intramolecular Arylation of Triphenylmethanols

Six new unsymmetrically substituted derivatives of 2-aminotriphenylmethanol (1) have been synthesised.The direction of ring closure following diazotisation and loss of nitrogen is determined by the nature of the intermediates formed.Where aryl radical intermediates are formed, the selectivity parallels that found in intermolecular competition by phenyl radicals, whereas copper-catalysed decomposition of the diazonium ion leads to intermediates which seem, from their selectivity, to possess considerable cationic nature.The slower thermal decomposition of the diazonium ions unexpectedly shows very little selectivity, suggesting that electrostatic interactions predominate in determining a very short lifetime of the crucial intermediate.