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| | 3-Acetamidophenylboronic acid Basic information |
| | 3-Acetamidophenylboronic acid Chemical Properties |
| Melting point | 135 °C (lit.) | | density | 1.23±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | soluble in Methanol | | pka | 8.04±0.10(Predicted) | | form | powder | | color | Light orange to Yellow to Green | | BRN | 3278316 | | InChI | 1S/C8H10BNO3/c1-6(11)10-8-4-2-3-7(5-8)9(12)13/h2-5,12-13H,1H3,(H,10,11) | | InChIKey | IBTSWKLSEOGJGJ-UHFFFAOYSA-N | | SMILES | CC(=O)Nc1cccc(c1)B(O)O | | CAS DataBase Reference | 78887-39-5(CAS DataBase Reference) | | EPA Substance Registry System | Boronic acid, B-[3-(acetylamino)phenyl]- (78887-39-5) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 22-24/25-36-26-37 | | WGK Germany | 3 | | F | 3-10 | | HazardClass | IRRITANT | | HS Code | 29310095 | | Storage Class | 11 - Combustible Solids |
| | 3-Acetamidophenylboronic acid Usage And Synthesis |
| Chemical Properties | Off-white to pale brown powder | | Uses | suzuki reaction | | Uses | Reactant involved in:
- Suzuki-Miyaura coupling reactions
- Trifluoromethylation
Reactant involved in the synthesis of a variety of inhibitors including:
- NR2B subtype of NMDA receptor antagonists for antidepressant activity
- Biphenylylmethylimidazole derivatives for use as 17,20-lyase inhibitors
- (Indolyl)-3,5-substituted benzene analogs with antimitotic and antitumor activity
- Substituted pyrrolidines and tetrahydrofurans as AMPA receptor positive modulators
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| | 3-Acetamidophenylboronic acid Preparation Products And Raw materials |
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