- 4-Methoxyphenyl boro
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- $5.90 / 1KG
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2021-11-15
- CAS:5720-07-0
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 500ton/Month
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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. | form | Crystalline Powder | pka | 8.96±0.10(Predicted) | 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 for Suzuki-Miyaura cross-coupling reactions Pd-catalyzed direct arylation Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water Palladium-catalyzed stereoselective Heck-type reaction Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides Ruthenium catalyzed direct arylation Rh-catalyzed asymmetric conjugate addition | Uses | suzuki reaction | Uses | 4-Methoxylphenylboronic Acid is a phenylboronic acid used to investigate boron function in plants. |
| 4-Methoxyphenylboronic acid Preparation Products And Raw materials |
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