Methylboronic Acid CAS 13061-96-6 Purity >98.0% Factory High Quality
Manufacturer Supply With High Quality, Commercial Production
Chemical Name: Methylboronic Acid CAS: 13061-96-6
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 |
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: 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.
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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.