| Phenylboronic acid Chemical Properties | |
| Melting point | 216-219 °C(lit.) |
| storage temp. | 0-6°C |
| form | Crystalline Powder |
| pka | 8.83(at 25℃) |
| color | White to off-white |
| Water Solubility | 10 g/L (20 ºC) |
| Sensitive | Hygroscopic |
| Merck | 14,1068 |
| BRN | 970972 |
| CAS DataBase Reference | 98-80-6(CAS DataBase Reference) |
| EPA Substance Registry System | Boronic acid, phenyl-(98-80-6) |
| Safety Information | |
| Hazard Codes | Xn,Xi,N |
| Risk Statements | 22-36/37/38-20/21/22 |
| Safety Statements | 22-24/25-36/37/39-26-36 |
| WGK Germany | 3 |
| RTECS | CY8575000 |
| Hazard Note | Harmful |
| TSCA | Yes |
| HazardClass | IRRITANT, MOISTURE SENSITIVE |
| HS Code | 29310095 |
| Phenylboronic acid Usage And Synthesis | |
| Chemical Properties | white to light yellow crystal powder |
| Uses | Reagent used for• ;Rhodium-catalyzed intramolecular amination1 • ;Pd-catalyzed direct arylation2 • ;Mizoroki-Heck and Suzuki-Miyaura coupling reactions catalyzed by palladium nanoparticles3 • ;Palladium-catalyzed stereoselective Heck-type reaction4 • ;Highly effective Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water5 Reagent used in Preparation of• ;Ni(II) pincer complex and Pd(II) pyridoxal hydrazone metallacycles as catalysts for the Suzuki-Miyaura cross-coupling reactions6,7• ;N-type polymers for all-polymer solar cells8 • |
| Uses | suzuki reaction |
| Uses | Phenylboronic Acid is a compound used in organic synthesis of various pharmaceutical goods. |
| Phenylboronic acid Preparation Products And Raw materials | |
| Preparation Products | Dimidium bromide-->3-AMINOBIPHENYL-->3-PHENYLBENZYLAMINE-->4-AMINOBIPHENYL-->1-phenyl-3-(trifluoromethyl)pyrazole-4-carboxylic acid-->3-AMINO-6-PHENYLPYRIDAZINE-->2-Aminophenylboronic acid |
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