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Isopropylboronic acid, 98%, Thermo Scientific Chemicals
Catalog number: L19962.06
5 g, Each
Thermo Scientific Chemicals
Isopropylboronic acid, 98%, Thermo Scientific Chemicals
Catalog number: L19962.06
5 g, Each
Quantity
Chemical Identifiers
CAS
80041-89-0
IUPAC Name
(propan-2-yl)boronic acid
Molecular Formula
C3H9BO2
InChI Key
QIPHSSYCQCBJAX-UHFFFAOYSA-N
SMILES
CC(C)B(O)O
Specifications
Specification SheetProton NMR
conforms to structure
Assay (Aqueous acid-base Titration)
≥97.5 to ≤102.5%
Melting Point (clear melt)
102-109?C
Appearance (Color)
White to cream
Form
Crystals or powder or crystalline powder or flakes or crystalline flakes
Description
Isopropylboronic acid as a reagent is involved in copper-promoted cross-coupling, Domino Heck-Suzuki reactions, Suzuki-Miyaura type couple reactions and alkylation-hydride reduction sequence.
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
Isopropylboronic acid as a reagent is involved in copper-promoted cross-coupling, Domino Heck-Suzuki reactions, Suzuki-Miyaura type couple reactions and alkylation-hydride reduction sequence.
Solubility
Soluble in water.
Notes
Hygroscopic. Incompatible with oxidizing agents.
Isopropylboronic acid as a reagent is involved in copper-promoted cross-coupling, Domino Heck-Suzuki reactions, Suzuki-Miyaura type couple reactions and alkylation-hydride reduction sequence.
Solubility
Soluble in water.
Notes
Hygroscopic. Incompatible with oxidizing agents.
RUO – Research Use Only
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