- 4-Iodophenylboronic acid
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- $15.00 / 1KG
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2021-07-13
- CAS:5122-99-6
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
- 4-Iodophenylboronic acid
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- $15.00 / 1KG
-
2021-07-10
- CAS:5122-99-6
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
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| | 4-Iodophenylboronic acid Basic information |
| | 4-Iodophenylboronic acid Chemical Properties |
| Melting point | 326-330 °C (lit.) | | Boiling point | 333.1±44.0 °C(Predicted) | | density | 1.95±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | soluble in Methanol | | pka | 8.29±0.10(Predicted) | | form | Powder | | color | Light beige | | Water Solubility | 25 g/L | | Sensitive | Light Sensitive | | InChIKey | PELJYVULHLKXFF-UHFFFAOYSA-N | | CAS DataBase Reference | 5122-99-6(CAS DataBase Reference) |
| | 4-Iodophenylboronic acid Usage And Synthesis |
| Chemical Properties | White crystalline powder | | Uses | Reagent used for
- Copper-mediated ligandless aerobic fluoroalkylation
- Palladium-catalyzed aerobic oxidative cross-coupling reactions
- Recyclable magnetic-nanoparticle-supported palladium catalyst for the Suzuki coupling reactions
- Oxidative hydroxylation using a copper (Cu) catalyst
- Ligand-free palladium-catalyzed Suzuki-Miyaura cross-coupling
- Homocoupling using gold salts as a catalyst
- Ruthenium (Ru)-catalyzed cross-coupling
- CuI-catalyzed Suzuki coupling reactions
- Palladium-catalyzed domino Heck-Mizoroki/Suzuki-Miyaura reactions
- Manganese triacetate-mediated radical additions of arylboronic acids to alkenes
Reagent used in Preparation of
- Pleuromutilin derivatives for ribosomal binding and antibacterial activity via "Click Chemistry"
- Liquid crystalline polyacetylene derivatives
| | Uses | suzuki reaction |
| | 4-Iodophenylboronic acid Preparation Products And Raw materials |
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