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| 4-Methoxyphenylboronic acid Basic information |
| 4-Methoxyphenylboronic acid Chemical Properties |
| Melting point | 204-206 °C(lit.) | | Boiling point | 306.8±44.0 °C(Predicted) | | density | 1.17±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Soluble in dimethyl sulfoxide and methanol. | | pka | 8.96±0.10(Predicted) | | form | Crystalline Powder | | color | White to light beige | | BRN | 2936912 | | CAS DataBase Reference | 5720-07-0(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | RTECS | CY8975000 | | TSCA | No | | HazardClass | IRRITANT | | HS Code | 29310095 |
| 4-Methoxyphenylboronic acid Usage And Synthesis |
| Chemical Properties | white to light beige crystalline powder | | Uses | 4-Methoxyphenylboronic acid can be used as a common organic reagent in Suzuki coupling reactions to study the N-arylation of imidazoles and amines catalyzed by copper exchange of calcium fluorophosphates.Reagent used in the preparation of various biological inhibitors. | | Uses | 4-Methoxyphenylboronic acid is a reagent used forSuzuki-Miyaura cross-coupling reactionsPd-catalyzed direct arylationHighly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in waterPalladium-catalyzed stereoselective Heck-type reactionTandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequenceCopper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides Ruthenium catalyzed direct arylationRh-catalyzed asymmetric conjugate addition | | Uses | 4-Methoxylphenylboronic Acid is a phenylboronic acid used to investigate boron function in plants. | | Uses | suzuki reaction |
| 4-Methoxyphenylboronic acid Preparation Products And Raw materials |
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