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| | 2,4-Dichlorophenylboronic acid Basic information |
| | 2,4-Dichlorophenylboronic acid Chemical Properties |
| Melting point | 246-249 °C (lit.) | | Boiling point | 331.3±52.0 °C(Predicted) | | density | 1.47±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | soluble in Methanol | | form | Powder | | pka | 8.10±0.58(Predicted) | | color | White to off-white | | BRN | 4983878 | | InChI | 1S/C6H5BCl2O2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,10-11H | | InChIKey | QNEGDGPAXKYZHZ-UHFFFAOYSA-N | | SMILES | OB(O)c1ccc(Cl)cc1Cl | | CAS DataBase Reference | 68716-47-2(CAS DataBase Reference) |
| Hazard Codes | Xn,Xi | | Risk Statements | 36/37/38-22 | | Safety Statements | 37/39-26-36 | | WGK Germany | 3 | | HazardClass | IRRITANT | | HS Code | 29163990 | | Storage Class | 11 - Combustible Solids |
| | 2,4-Dichlorophenylboronic acid Usage And Synthesis |
| Chemical Properties | white to off-white powder | | Uses | 2,4-Dichlorophenylboronic acid is used as reactant involved in:
• Suzuki coupling reactions with alkynyl bromides or aniline / thiophenol
• Selective hydroxylation to phenols4Reactant involved in synthesis of biologically active molecules including:
• N-hydroxyindole-2-carboxylates for use as lactate dehydrogenase inhibitors
• Non-ATP competitive MK2 inhibitors | | Uses | suzuki reaction | | Uses | Reactant involved in:
- Suzuki coupling reactions with alkynyl bromides or aniline / thiophenol
- Selective hydroxylation to phenols
Reactant involved in synthesis of biologically active molecules including:
- N-hydroxyindole-2-carboxylates for use as lactate dehydrogenase inhibitors
- Non-ATP competitive MK2 inhibitors
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| | 2,4-Dichlorophenylboronic acid Preparation Products And Raw materials |
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