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4-n-Butoxybenzeneboronic acid, 98%, Thermo Scientific Chemicals
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Price (USD)/ Each
125.00
4-n-Butoxybenzeneboronic acid, 98%, Thermo Scientific Chemicals
Catalog numberH52865.06
Price (USD)/ Each
125.00
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Chemical Identifiers
CAS105365-51-3
IUPAC Name(4-butoxyphenyl)boronic acid
Molecular FormulaC10H15BO3
InChI KeyQUPFQMXWFNJUNJ-UHFFFAOYSA-N
SMILESCCCCOC1=CC=C(C=C1)B(O)O
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Specifications
Specification Sheet
Specification SheetAssay (HPLC)>97.5%
Used as a reactant for Suzuki-Miyaura cross-coupling reactions, condensation reactions, synthesis of azobenzene-functionalized compounds. Also used for preparation of highly fluorescent diketopyrrolopyrrole derivatives, rhodium-catalyzed Suzuki-type cross-coupling and copper-catalyzed asymmetric conjugate reduction of coumarins.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Used as a reactant for Suzuki-Miyaura cross-coupling reactions, condensation reactions, synthesis of azobenzene-functionalized compounds. Also used for preparation of highly fluorescent diketopyrrolopyrrole derivatives, rhodium-catalyzed Suzuki-type cross-coupling and copper-catalyzed asymmetric conjugate reduction of coumarins.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
Used as a reactant for Suzuki-Miyaura cross-coupling reactions, condensation reactions, synthesis of azobenzene-functionalized compounds. Also used for preparation of highly fluorescent diketopyrrolopyrrole derivatives, rhodium-catalyzed Suzuki-type cross-coupling and copper-catalyzed asymmetric conjugate reduction of coumarins.
Solubility
Slightly soluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
RUO – Research Use Only
General References:
- Elena Zaborova et. al. Cavitand supported tetraphosphine: cyclodextrin offers a useful platform for Suzuki-Miyaura cross-coupling. Chemical Communications. 2011, 47 (32), 9206-9208.
- Samuel Reyes; Robert W Huigens; Zhaoming Su; Michel L Simon; Christian Melander. Synthesis and biological activity of 2-aminoimidazole triazoles accessed by Suzuki-Miyaura cross-coupling. Organic & Biomolecular Chemistry. 2011, 9 (8), 3041-3049.