- Methylboronic acid
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- $10.00 / 1ASSAYS
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2025-12-08
- CAS:13061-96-6
- Min. Order: 1ASSAYS
- Purity: 99%
- Supply Ability: 1 ton
- Methylboronic acid
-
- $1.90 / 1KG
-
2025-05-26
- CAS:13061-96-6
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 10 ton
- Methylboronic acid
-
- $0.00 / 1kg
-
2025-04-04
- CAS:13061-96-6
- Min. Order: 1kg
- Purity: 98%
- Supply Ability: 1Ton
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| | Methylboronic acid Basic information |
| | Methylboronic acid Chemical Properties |
| Melting point | 91-94 °C (lit.) | | Boiling point | 141.7±23.0 °C(Predicted) | | density | 0.965±0.06 g/cm3(Predicted) | | storage temp. | Inert atmosphere,Store in freezer, under -20°C | | solubility | DMSO, Water | | pka | 9.97±0.43(Predicted) | | form | Crystalline Powder | | color | White to off-white | | Water Solubility | Soluble in water. | | Sensitive | Hygroscopic | | BRN | 1731087 | | InChI | InChI=1S/CH5BO2/c1-2(3)4/h3-4H,1H3 | | InChIKey | KTMKRRPZPWUYKK-UHFFFAOYSA-N | | SMILES | CB(O)O | | CAS DataBase Reference | 13061-96-6(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | F | 3-10 | | Hazard Note | Irritant/Keep Cold | | HazardClass | IRRITANT | | HS Code | 29319090 |
| | Methylboronic acid Usage And Synthesis |
| Chemical Properties | White to light yellow crystal powde | | Uses | 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.
- For derivatizing many carbohydrates and biologically active compounds for GLC analysis.
| | Uses | suzuki reaction | | Uses | Methylboronic Acid is a methylated derivative of boronic acid, a building block towards various intermediates in suzuki coupling. |
| | Methylboronic acid Preparation Products And Raw materials |
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