Methylboronic acid, 97%, Thermo Scientific Chemicals
Methylboronic acid, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Methylboronic acid, 97%, Thermo Scientific Chemicals

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Quantity:
5 g
1 g
Catalog number L15589.06
also known as L15589-06
Price (USD)/ Each
140.65
Online exclusive
156.00 
Save 15.35 (10%)
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Quantity:
5 g
Request bulk or custom format
Price (USD)/ Each
140.65
Online exclusive
156.00 
Save 15.35 (10%)
Add to cart
Methylboronic acid, 97%, Thermo Scientific Chemicals
Catalog numberL15589.06
Price (USD)/ Each
140.65
Online exclusive
156.00 
Save 15.35 (10%)
-
Add to cart
Chemical Identifiers
CAS13061-96-6
IUPAC Namemethylboronic acid
Molecular FormulaCH5BO2
InChI KeyKTMKRRPZPWUYKK-UHFFFAOYSA-N
SMILESCB(O)O
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White to cream
FormCrystals or powder or crystalline powder or lumps or fused solid
Assay (Aqueous acid-base Titration)≥96.0%
Identification (FTIR)Conforms
Proton NMRConforms to structure
Reagent used for palladium-catalyzed stille and suzuki-miyaura cross-couplings, microwave-heated heterogeneous palladium (pd)-catalytized reactions, ruthenium (ru)-catalyzed silylation reactions, bis(aminotropone) titanium (ti) catalysts for ethylene polymerizations, enantioselective asymmetric bromoaminocyclization and bromoaminocyclization using amino-thiocarbamate catalysts. Reagent used in preparation of common building blocks for pharmaceuticals and agrochemicals, chrysin analogs by suzuki-miyaura coupling reactions, casein kinase i inhibitors, divergent c-h functionalizations directed by sulfonamide pharmacophores in drug discovery.

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
Reagent used for palladium-catalyzed stille and suzuki-miyaura cross-couplings, microwave-heated heterogeneous palladium (pd)-catalytized reactions, ruthenium (ru)-catalyzed silylation reactions, bis(aminotropone) titanium (ti) catalysts for ethylene polymerizations, enantioselective asymmetric bromoaminocyclization and bromoaminocyclization using amino-thiocarbamate catalysts. Reagent used in preparation of common building blocks for pharmaceuticals and agrochemicals, chrysin analogs by suzuki-miyaura coupling reactions, casein kinase i inhibitors, divergent c-h functionalizations directed by sulfonamide pharmacophores in drug discovery.

Solubility
Soluble in water.

Notes
Hygroscopic.Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, water, moisture.
RUO – Research Use Only

General References:

  1. Ben W Glasspoole et. al. Suzuki-Miyaura cross-couplings of secondary allylic boronic esters.. Chemical Communications. 2012, 48 (9), 1230-1232 .
  2. Hui-Xiong Dai et. al. Divergent C-H functionalizations directed by sulfonamide pharmacophores: late-stage diversification as a tool for drug discovery.. Journal of the American Chemical Society. 2011, 133 (18), 7222-7228.