IUPAC Name: | methylboronic acid |
Description: | 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 catalystsReagent 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. |
Molecular Weight: | 59.86 |
Molecular Formula: | CH5O2B |
Canonical SMILES: | B(C)(O)O |
InChI: | InChI=1S/CH5BO2/c1-2(3)4/h3-4H,1H3 |
InChI Key: | KTMKRRPZPWUYKK-UHFFFAOYSA-N |
Boiling Point: | 141.7 °C at 760 mmHg |
Melting Point: | 91-94 °C (lit.) |
Flash Point: | Not applicable |
Purity: | 97 % |
Density: | 0.965 g/cm3 |
MDL: | MFCD00002105 |
LogP: | -0.91100 |
Customer Support
If the product you need is not in our catalog, please contact us in time to submit your needs. You can help our website get better and better. Why not submit the request today?
Customer Centered
Related Functional Groups
Boronic Acids and Esters
2-(7,8-Difluoro-1-naphthyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
4-(3,5-Dimethyl-1-pyrazolyl)phenylboronic Acid Pinacol Ester
Customers Also Viewed
Copyright © 2025 BOC Sciences. All rights reserved.
Our Products