| Identification | Back Directory | [Name]
Benzo[C][1,2,5]thiadiazole-5-boronic acid pinacol ester, 97% | [CAS]
1168135-03-2 | [Synonyms]
Benzo[C][1,2,5]thiadiazole-5-boronic acid pinacol ester, 97%
2,1,3-Benzothiadiazole, 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[c][1,2,5]thiadiazole
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole, 2-(2,1,3-Benzothiadiazol-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | [Molecular Formula]
C12H15BN2O2S | [MDL Number]
MFCD11867874 | [MOL File]
1168135-03-2.mol | [Molecular Weight]
262.14 |
| Chemical Properties | Back Directory | [Melting point ]
81-86°C | [Boiling point ]
366.3±15.0 °C(Predicted) | [density ]
1.22±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [form ]
Powder | [pka]
-0.02±0.36(Predicted) | [color ]
Brown |
| Hazard Information | Back Directory | [Uses]
Benzo[c][1,2,5]thiadiazol-5-ylboronic acid pinacol ester can be used as a reactant:
- To synthesize 5-methylbenzo[c][1,2,5]thiadiazole by methylation reaction with methyl iodide using palladium catalyst.
- In the Miyaura borylation and Suzuki coupling reactions.
- To prepare benzothiadiazole derivatives as potent PFKFB3 kinase inhibitors.
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