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| 4-Bromophenylboronic acid Basic information |
| 4-Bromophenylboronic acid Chemical Properties |
| Melting point | 284-288 °C (lit.) | | Boiling point | 315.0±44.0 °C(Predicted) | | density | 1.67±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | form | Crystalline Powder | | pka | 8.32±0.10(Predicted) | | color | Off-white to light beige | | Water Solubility | Soluble in methanol. Insoluble in water. | | BRN | 2936347 | | InChIKey | QBLFZIBJXUQVRF-UHFFFAOYSA-N | | CAS DataBase Reference | 5467-74-3(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38-22 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | RTECS | CY8650000 | | TSCA | T | | HazardClass | IRRITANT | | HS Code | 29319090 |
| 4-Bromophenylboronic acid Usage And Synthesis |
| Chemical Properties | white to light yellow crystal powde | | Uses | suzuki reaction | | Uses | 4-Bromobenzeneboronic acid is a reagent used for Palladium catalyzed Suzuki-Miyaura cross-couplings, Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence. It is also used in the preparation of Protein modulators and enzymatic and kinase inhibitors, Gallate-based obovatol analogs with potential anti-tumor activity. It is used as a reagent for Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides, Pd-catalyzed arylative cyclization of alkyne-tethered enals or enones via carbopalladation of alkynes, Copper-catalyzed cross-couplings. | | Uses | Labelled 4-Bromophenylboronic Acid (B686545). 4-Bromophenylboric acid is used in the preparation of arylboronates as inhibitors of fatty acid amide hydrolase. |
| 4-Bromophenylboronic acid Preparation Products And Raw materials |
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