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| IUPAC Name: | (5-bromopyridin-3-yl)boronic acid |
| Description: | Reactant for preparation of: Thienylpyridyl garlands via cross-coupling with heteroaryl halides; Arenes via nickel-catalyzed cross-coupling with potassium aryl- and heteroaryl trifluoroborates; Meso-substituted ABCD-type porphyrins by functionalization reactions; Analogs of (acetylamino)(dimethylpyrazol)(pyridyl)pyrimidines as A2A adenosine receptor antagonists for the treatment of Parkinson's disease; 5-hydroxy-1,3,2-dioxaborolan-4-ones boronate-amine complexes via heterocyclization with α-oxocarboxylic acids followed by subsequent complexation; Radioligands with optimized brain kinetics for PET imaging of nAChR. |
| Molecular Weight: | 201.82 |
| Molecular Formula: | C5H5BBrNO2 |
| Canonical SMILES: | B(C1=CC(=CN=C1)Br)(O)O |
| InChI: | InChI=1S/C5H5BBrNO2/c7-5-1-4(6(9)10)2-8-3-5/h1-3,9-10H |
| InChI Key: | ICCGFOKNFZWCTJ-UHFFFAOYSA-N |
| Melting Point: | 260 °C (dec.) |
| Purity: | 96 % |
| Storage: | 2-8 °C |
| MDL: | MFCD02685634 |
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Boronic Acids and Esters
4-(3,5-Dimethyl-1-pyrazolyl)phenylboronic Acid Pinacol Ester
Halides
1-(3-Chloro-4-methylphenyl)-3-(trifluoromethyl)pyrazole-5-ylamine
Pyridines
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