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571490 Aldrich

9,9-Didodecylfluorene-2,7-diboronic acid

97%

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents,
InChI Key   MLGWUNIPUPZNEE-UHFFFAOYSA-N
assay   97%
mp   269 °C (Dec.)(lit.)

Description

Packaging

1, 5 g in glass bottle

Application

Reactant involved in synthesis of:
• Luminescent alternating boron quinolate-fluorene copolymers
• C nanotube composites for polymer memory devices via Suzuki coupling reactions
• Fluorine-containing fluorene oligomers

Price and Availability


KitAlysis - Increasing Catalysis Productivity

Cross-Coupling Guide
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Boronic Acids - Aldrich ChemFiles 2007, 7.7, 3.

Most boronic acids readily undergo dehydration reactions to give a cyclic (trimer) anhydride. Our selection of boronic acids may contain varying amounts of this cyclic anhydride. Fortunately, the aci...
Aldrich ChemFiles 2007, 7.7, 3.
Keywords: Chemfiles, Coupling reactions, Dehydration reaction, Suzuki coupling

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