- 4-Methoxyphenyl boro
-
- $5.90 / 1KG
-
2021-11-15
- CAS:5720-07-0
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 500ton/Month
|
| | 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 |
|