Methylboronic Acid CAS 13061-96-6 Purity >98.0% (Titration)
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 |
Stock Status | In Stock, Production Scale Up to Tons |
Molecular Formula | CH5BO2 |
Molecular Weight | 59.86 |
Melting Point | 91.0~94.0℃(lit.) |
Density | 0.965±0.06 g/cm3 |
Water Solubility | Soluble in Water |
Sensitive | Hygroscopic |
COA & MSDS | Available |
Place of Origin | Shanghai, China |
Brand | Ruifu Chemical |
Item | Specifications | Results |
Appearance | White Crystals | White Crystals |
Methylboronic Acid Purity | >98.0% (Neutralization Titration) | 98.25% |
Melting Point | 87.0~94.0℃ | 90.5℃ |
Total Impurities | <2.00% | Conforms |
Infrared Spectrum | Conforms to Structure | Conforms |
1H NMR Spectrum | Conforms to Structure | Conforms |
Test Standard | Enterprise Standard | Conforms |
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.
Hazard Symbols Xi - Irritant
Risk Codes 36/37/38 - Irritating to eyes, respiratory system and skin.
Safety Description
S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
WGK Germany 3
FLUKA BRAND F CODES 3-10
HS Code 2931900090
Hazard Note Irritant/Keep Cold
Hazard Class IRRITANT
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 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.