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Methylboronic acid, 97%, Thermo Scientific Chemicals

Catalog Number 11388336
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Quantity:
1 g
5 g
This item is not returnable. View return policy
13061-96-6
CH5BO2
59.86
MFCD00002105
KTMKRRPZPWUYKK-UHFFFAOYSA-N
methaneboronic acid, methyl boronic acid, dihydroxymethylborane, boronic acid, methyl, unii-8z1me41sch, methane boronic acid, 8z1me41sch, methylboronicacid, methyboronic acid, methyl-boronic acid
139377
methylboronic acid
CB(O)O
This item is not returnable. View return policy
13061-96-6
CH5BO2
59.86
MFCD00002105
KTMKRRPZPWUYKK-UHFFFAOYSA-N
methaneboronic acid, methyl boronic acid, dihydroxymethylborane, boronic acid, methyl, unii-8z1me41sch, methane boronic acid, 8z1me41sch, methylboronicacid, methyboronic acid, methyl-boronic acid
139377
methylboronic acid
CB(O)O

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.
TRUSTED_SUSTAINABILITY
Melting Point 89°C to 94°C
Odor Odorless
Linear Formula CH3B(OH)2
Quantity 5 g
Beilstein 1731087
Sensitivity Hygroscopic
Solubility Information Soluble in water.
Formula Weight 59.86
Percent Purity 97%
Chemical Name or Material Methylboronic acid

RUO – Research Use Only

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