missing translation for 'onlineSavingsMsg'
Learn More

Methylboronic acid, 97%

Product Code. 11388336
Change view
Click to view available options
Quantity:
1 g
5 g
Unit Size:
1g
5g
2 product options available for selection
Product selection table with 2 available options. Use arrow keys to navigate and Enter or Space to select.
Product Code. Quantity Unit Size
11388336 5 g 5g
11378336 1 g 1g
Use arrow keys to navigate between rows. Press Enter or Space to select a product option. 2 options available.
2 options
This item is not returnable. View return policy
Product Code. 11388336 Supplier Thermo Scientific Alfa Aesar Supplier No. L15589.06
 Restricted Item
In Stock
Add to basket
This item is not returnable. View return policy

CAS: 13061-96-6 | CH5BO2 | 59.86 g/mol

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

Chemical Identifiers

CAS 13061-96-6
Molecular Formula CH5BO2
Molecular Weight (g/mol) 59.86
MDL Number MFCD00002105
InChI Key KTMKRRPZPWUYKK-UHFFFAOYSA-N
Synonym methaneboronic acid, methyl boronic acid, dihydroxymethylborane, boronic acid, methyl, unii-8z1me41sch, methane boronic acid, 8z1me41sch, methylboronicacid, methyboronic acid, methyl-boronic acid
PubChem CID 139377
IUPAC Name methylboronic acid
SMILES CB(O)O

Specifications

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

Product Title
Selezionare un problema

Facendo clic su Invia, l'utente riconosce che potrebbe essere contattato da Fisher Scientific in merito al feedback fornito in questo modulo. Non condivideremo le vostre informazioni per altri scopi. Tutte le informazioni di contatto fornite saranno conservate in conformità con la nostra Politica sulla privacy. Informativa sulla privacy.