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| IUPAC Name: | (2-chloropyridin-3-yl)boronic acid |
| Description: | Reactant for: Synthesis of Et canthinone-3-carboxylates from Et 4-bromo-6-methoxy-1,5-naphthyridine-3-carboxylate via a Pd-catalyzed Suzuki-Miyaura coupling and a Cu-catalyzed amidation reaction; Preparation of arylmethylpyrrolidinylmethanols and amine derivatives via reaction with MIDA followed by Suzuki reaction with halides or amination with amines; Preparation of arylazabicyclooctane derivatives as potential arginine vasopressin receptor antagonists; Regioselective preparation of halo-oligopyridines and oligopyridines by the Suzuki-Miyaura cross-coupling reaction May contain varying amounts of anhydride. |
| Molecular Weight: | 157.36 |
| Molecular Formula: | C5H5ClNO2B |
| Canonical SMILES: | B(C1=C(N=CC=C1)Cl)(O)O |
| InChI: | InChI=1S/C5H5BClNO2/c7-5-4(6(9)10)2-1-3-8-5/h1-3,9-10H |
| InChI Key: | VRDAOVQZVXYRNH-UHFFFAOYSA-N |
| Boiling Point: | 349.3 °C at 760 mmHg |
| Melting Point: | 121-134 °C |
| Flash Point: | Not applicable |
| Density: | 1.41 g/cm3 |
| Storage: | 2-8 °C |
| MDL: | MFCD03094997 |
| LogP: | -0.58520 |
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Boronic Acids and Esters
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