- 3-Bromophenylboronic acid
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- $34.00 / 1kg
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2024-04-08
- CAS:89598-96-9
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | 3-Bromophenylboronic acid Basic information |
| | 3-Bromophenylboronic acid Chemical Properties |
| Melting point | 164-168 °C (lit.) | | Boiling point | 330.5±44.0 °C(Predicted) | | density | 1.67±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | DMSO (Slightly), Methanol (Slightly) | | pka | 7.55±0.10(Predicted) | | form | Crystalline Powder | | color | White | | BRN | 3127104 | | CAS DataBase Reference | 89598-96-9(CAS DataBase Reference) |
| Hazard Codes | Xn,Xi | | Risk Statements | 36/37/38-22 | | Safety Statements | 37/39-26 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29319090 |
| | 3-Bromophenylboronic acid Usage And Synthesis |
| Chemical Properties | white to light yellow crystal powder | | Uses | Reactant involved in a variety of organic reactions including:
- Oxidative cross coupling
- Gold salt catalyzed homocoupling
- 1,4-Addition reactions with α,β-unsaturated ketones
- Enantioselective addition reactions
- Suzuki-Miyaura coupling for synthesis of anthranilamide-protected arylboronic acids
- C-H Functionalization of quinones
| | Uses | suzuki reaction | | Uses | Reactant involved in a variety of organic reactions including:• ;Oxidative cross coupling1,2• ;Gold salt catalyzed homocoupling3• ;1,4-Addition reactions with α,β-unsaturated ketones4• ;Enantioselective addition reactions5• ;Suzuki-Miyaura coupling for synthesis of anthranilamide-protected arylboronic acids6• ;C-H Functionalization of quinones7 |
| | 3-Bromophenylboronic acid Preparation Products And Raw materials |
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