Methylboronic Acid CAS 13061-96-6 Purity >98.0% Factory High Quality

Short Description:

Chemical Name: Methylboronic Acid 

CAS: 13061-96-6

Purity: >98.0%

Appearance: White Crystals

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com


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Description:

Manufacturer Supply With High Quality, Commercial Production 
Chemical Name: Methylboronic Acid CAS: 13061-96-6

Chemical Properties:

Chemical Name Methylboronic Acid
Synonyms Methaneboronic Acid
CAS Number 13061-96-6
CAT Number RF-PI1437
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula CH5BO2
Molecular Weight 59.86 
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance White Crystals
Purity / Analysis Method >98.0%
Melting Point 87.0~94.0℃
1H NMR Consistent With Structure
Infrared Spectrum Conforms to Structure
Total Impurities <2.00%
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates

Package & Storage:

Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture.

Advantages:

1

FAQ:

Application:

Methylboronic Acid (CAS: 13061-96-6) is a methylated derivative of boronic acid, a building block towards various intermediates in suzuki coupling, has many applications in organic synthesis. Methylboronic Acid can be used as a reagent: In the palladium-catalyzed Stille and Suzuki-Miyaura cross-couplings. In the microwave-heated heterogeneous palladium (Pd)-catalytized reactions. In ruthenium (Ru)-catalyzed silylation reactions To prepare bis(aminotropone) titanium (Ti) catalysts for ethylene polymerizations. In the enantioselective asymmetric bromoaminocyclization and bromoaminocyclization using amino-thiocarbamate catalysts. To prepare common building blocks for pharmaceuticals and agrochemicals. To prepare chrysin analogs by Suzuki-Miyaura coupling reactions. To prepare casein kinase I inhibitors. In the divergent C-H functionalizations directed by sulfonamide pharmacophores in drug discovery. In the synthesis of unsymmetrical monosulfides from disulfides via copper-catalyzed coupling with boronic acids. In a palladium-catalyzed coupling with enol tosylates. It is an important intermediate for the preparation of many boric acid derivatives such as (S) or (R) -2-Methyl-CBS-oxazaborolidine.

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