Other grades of this product :
| 4-Chlorophenylboronic acid Basic information |
| 4-Chlorophenylboronic acid Chemical Properties |
| Melting point | 284-289 °C(lit.) | | Boiling point | 295.4±42.0 °C(Predicted) | | density | 1.32±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | DMSO | | pka | 8.39±0.10(Predicted) | | form | Crystalline Powder | | color | Off-white to beige | | Water Solubility | 2.5 g/100 mL | | BRN | 2936346 | | InChIKey | CAYQIZIAYYNFCS-UHFFFAOYSA-N | | CAS DataBase Reference | 1679-18-1(CAS DataBase Reference) |
| 4-Chlorophenylboronic acid Usage And Synthesis |
| Chemical Properties | off-white to beige crystalline powder | | Uses | suzuki reaction | | Uses | 4-Chlorobenzeneboronic Acid is used as a catalyst for the preparation of 4-hydroxycoumarin derivatives which display antitrypanosomal and antioxidant properties. It is also used as a catalyst for the
asymmetric borane reduction of electron-deficient ketones. | | Uses | 4-Chlorophenylboronic acid can be used as a reactant in:- Palladium-catalyzed direct arylation.
- Cyclopalladation.
- Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation.
- Copper-mediated ligandless aerobic fluoroalkylation.
- Pd-catalyzed arylative cyclization.
- Ruthenium catalyzed direct arylation.
- Ligand-free copper-catalyzed coupling reactions.
- Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions.
It can also be used to prepare: - Substituted diarylmethylidenefluorenes via Suzuki coupling reaction.
- Baclofen lactam by Suzuki coupling of a pyrrolinyl tosylate, followed by hydrogenation reaction.
- Palladium(II) thiocarboxamide complexes as Suzuki coupling catalysts.
- Biaryls by Suzuki reactions of aryl chlorides, bromides, and iodides with arylboronic acids.
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| 4-Chlorophenylboronic acid Preparation Products And Raw materials |
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