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| IUPAC Name: | (2-bromophenyl)boronic acid |
| Description: | Catalyzes the formation of amide bonds from amines and carboxylic acids. Used to promote greener amidations of carboxylic acids and amines in catalytic amounts. This technology avoids the requirement of preactivation of the carboxylic acid or use of coupling reagents.Direct Amidation of Carboxylic Acids Catalyzed by ortho-Iodo Arylboronic Acids: Catalyst Optimization, Scope, and Preliminary Mechanistic Study Supporting a Peculiar Halogen Acceleration Effect. |
| Molecular Weight: | 200.83 |
| Molecular Formula: | C6H6BrO2B |
| Canonical SMILES: | B(C1=CC=CC=C1Br)(O)O |
| InChI: | InChI=1S/C6H6BBrO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H |
| InChI Key: | PLVCYMZAEQRYHJ-UHFFFAOYSA-N |
| Boiling Point: | 329.2 °C at 760 mmHg |
| Melting Point: | 113 °C (lit.) |
| Purity: | 99 % |
| Density: | 1.67 ± 0.1 g/mL (predicted) |
| Appearance: | White powder |
| MDL: | MFCD01114672 |
| LogP: | 0.12890 |
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Boronic Acids and Esters
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