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| | 3-ETHOXYPHENYLBORONIC ACID Basic information |
| | 3-ETHOXYPHENYLBORONIC ACID Chemical Properties |
| Melting point | 139-146 °C(lit.) | | Boiling point | 328.3±44.0 °C(Predicted) | | density | 1.13±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | solubility | soluble in Methanol | | form | Crystalline Powder | | pka | 8.14±0.10(Predicted) | | color | White to off-white | | InChI | 1S/C8H11BO3/c1-2-12-8-5-3-4-7(6-8)9(10)11/h3-6,10-11H,2H2,1H3 | | InChIKey | CHCWUTJYLUBETR-UHFFFAOYSA-N | | SMILES | CCOc1cccc(c1)B(O)O | | CAS DataBase Reference | 90555-66-1(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36/37/39-36 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29163990 | | Storage Class | 11 - Combustible Solids |
| | 3-ETHOXYPHENYLBORONIC ACID Usage And Synthesis |
| Chemical Properties | white to light yellow crystal powde | | Uses | suzuki reaction | | Uses | 3-Ethoxyphenylboronic Acid is a useful research reagent for the synthesis of biologically active molecules. | | Uses | Reactant involved in:
- Cyanation for synthesis of aromatic and vinyl nitriles
- Microwave-assisted palladium-catalyzed arylation of resin supported pyrazinones
- Copper-mediated N- and O-arylations
Reactant involved in synthesis of biologically active molecules including:
- Amino derivatives of indole for use as isoprenylcysteine carboxyl methyltransferase inhibitors
- 5-Arylindazole glucocorticoid receptor agonists and antagonists
- 1,5-Diaryl-1,2,4-triazoles as cis-restricted combretastatin analogs
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| | 3-ETHOXYPHENYLBORONIC ACID Preparation Products And Raw materials |
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