| Identification | Back Directory | [Name]
3-Methoxythiophene-2-boronic acid pinacol ester | [CAS]
1310384-98-5 | [Synonyms]
3-Methoxythiophene-2-boronic acid pinacol ester
3-Methoxythiophene-2-boronic acid pinacol ester 97%
4,4,5,5-Tetramethyl-2-(3-methoxy-2-thienyl)-1,3,2-dioxaborolane
1,3,2-Dioxaborolane, 2-(3-methoxy-2-thienyl)-4,4,5,5-tetramethyl- | [Molecular Formula]
C11H17BO3S | [MDL Number]
MFCD09837621 | [MOL File]
1310384-98-5.mol | [Molecular Weight]
240.13 |
| Chemical Properties | Back Directory | [Melting point ]
124-128°C | [Boiling point ]
333.1±27.0 °C(Predicted) | [density ]
1.10±0.1 g/cm3(Predicted) | [storage temp. ]
-20°C, sealed storage, away from moisture | [form ]
solid | [Appearance]
White to off-white Solid | [InChI]
1S/C11H17BO3S/c1-10(2)11(3,4)15-12(14-10)9-8(13-5)6-7-16-9/h6-7H,1-5H3 | [InChIKey]
FXKKXDGOIQJEJS-UHFFFAOYSA-N | [SMILES]
COc1ccsc1B2OC(C)(C)C(C)(C)O2 |
| Hazard Information | Back Directory | [Uses]
3-Methoxythiophene-2-boronic acid pinacol ester can be used:
- As an intermediate in the synthesis of benzothiadiazole derivatives, which are used as building blocks in the preparation of organic semiconductors.
- As a starting material in the synthesis of imidazo[1,2-a]pyridine derivatives exhibiting bright excited-state intramolecular proton transfer (ESIPT) luminescence property in solid-state.
- As a starting material in the preparation of polycyclic aromatic triptycenes.
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