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| IUPAC Name: | (2-formylthiophen-3-yl)boronic acid |
| Description: | 2-Formyl-3-thiopheneboronic acid can be used as: A substrate in the palladium-Tedicyp catalyzed Suzuki coupling reaction with different aryl bromides; A starting material for the synthesis of 4H-thieno[2,3-c]-isoquinolin-5-one derivatives as PARP-1 inhibitors; A starting material for the preparation of phenanthro-dithiophene moieties having field-effect transistor properties. Reactant for: Suzuki cross-coupling reactions; Preparation of boronic acid esters. |
| Molecular Weight: | 155.97 |
| Molecular Formula: | C5H5BO3S |
| Canonical SMILES: | B(C1=C(SC=C1)C=O)(O)O |
| InChI: | InChI=1S/C5H5BO3S/c7-3-5-4(6(8)9)1-2-10-5/h1-3,8-9H |
| InChI Key: | BBENFHSYKBYWJX-UHFFFAOYSA-N |
| Boiling Point: | 396.7 °C at 760 mmHg |
| Melting Point: | 167-193 °C (lit.) |
| Flash Point: | Not applicable |
| Purity: | 95 % |
| Density: | 1.41 g/cm3 |
| MDL: | MFCD01075678 |
| LogP: | -0.75960 |
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Flexible batch size for diverse industrial demandsRelated Functional Groups
Boronic Acids and Esters
2-(3-Hydroxyphenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione
Carbonyl Compounds
1-{2-[(3-Methoxypropyl)amino]-4-methyl-1,3-thiazol-5-yl}ethanone hydrochloride
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