849222-39-5

Basic information

• Product Name: 9H-Fluoren-9-ol, 2-bromo-9-[4-(1,1-dimethylethyl)phenyl]-
• CAS NO: 849222-39-5
• Molecular Formula: C23H21BrO
• Molecular Weight: 393.323
• Mol File: 849222-39-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 9H-Fluoren-9-ol, 2-bromo-9-[4-(1,1-dimethylethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 9H-Fluoren-9-ol, 2-bromo-9-[4-(1,1-dimethylethyl)phenyl]-(849222-39-5)
• EPA Substance Registry System: 9H-Fluoren-9-ol, 2-bromo-9-[4-(1,1-dimethylethyl)phenyl]-(849222-39-5)

Safety Data

• Hazardous Substances Data: 849222-39-5(Hazardous Substances Data)

Upstream product

• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 3096-56-8 2-bromofluoren-9-one 
• 63488-10-8 4-tert-butylmagnesium bromide 
• 486-25-9 9-fluorenone 

Downstream Products

• 869565-71-9 2-(1,1,2,2-tetramethyl(ethyleneboronato))-9-(4-tert-butylphenyl)-9-(4-hydroxyphenyl)fluorene 
• 849222-41-9 (C₁₃H₇OC₆H₆C₄H₈C₆H₄)2C₁₃H₆C₁₂H₂₆ 
• 873371-53-0 (C₁₃H₇OC₆H₆C₄H₈C₆H₄)2 

Relevant articles and documents

Compound, Coating Composition Comprising Same, and Organic Light-Emitting Device

The present specification relates to a compound, a coating composition including the same, and an organic light emitting device.

Synthesis and electrooptical properties of copolymers derived from phenol-functionalized telechelic oligofluorenes

This paper describes the synthesis, characterization, and electrooptical properties of a series of phenol-capped, discrete oligofluorenes with 2, 3, 5, and 7 fluorene units and a statistical oligomer with an average of about 10 fluorene units. Polymers were prepared from the oligomers by various linking reactions through the phenol groups. High molecular weight polycarbonate polymers derived from these oligomers were prepared using BPA-bis-chloroformate (BPABCF) as the linking group. Trends in the optical and electrical properties as a function of oligomer length are reported, Device data for this family of emissive copolymers indicates that charge mobility increases with conjugation length and can be better than that of an analogue homopolymer, A surprising shift in LUMO values due to CFs substitution at the ends of the oligomers was observed.