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- Chemistry
- Asymmetric Synthesis
- Chiral Building Blocks
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- C-H Activation
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| Structure chimique | Catalogue N° | CAS N° | Formule | Masse moléculaire |
|---|
 |
BD161503 | 1072944-18-3 | C6H7BFNO2 | 154.94 |
| 2-Fluoro-4-methyl-5-pyridineboronic acid | ||||
 |
BD35093 | 847664-64-6 | C5H4BCl2NO2 | 191.81 |
| 2,5-Dichloropyridine-4-boronic acid | ||||
 |
BD14108 | 68716-48-3 | C12H16BNO4 | 249.07 |
| 4,4,5,5-Tetramethyl-2-(3-nitrophenyl)-1,3,2-dioxaborolane | ||||
 |
BD3772 | 221006-70-8 | C7H10BNO4 | 182.97 |
| 2,6-Dimethoxypyridin-3-ylboronic acid | ||||
 |
BD196767 | 957121-09-4 | C7H7BBrFO2 | 232.84 |
| (2-Bromo-6-fluoro-3-methylphenyl)boronic acid | ||||
 |
BD8256 | 845551-44-2 | C13H12BClO3 | 262.50 |
| (4-(Benzyloxy)-3-chlorophenyl)boronic acid | ||||
![Benzo[b]thiophen-3-ylboronic acid](https://file.bldpharm.com/static/upload/proimg/510/113893-08-6.png) |
BD6033 | 113893-08-6 | C8H7BO2S | 178.02 |
| Benzo[b]thiophen-3-ylboronic acid | ||||
 |
BD35040 | 832695-88-2 | C8H10BNO3 | 178.98 |
| (3-(Methylcarbamoyl)phenyl)boronic acid | ||||
 |
BD16417 | 68716-52-9 | C16H19BO2 | 254.13 |
| 4,4,5,5-Tetramethyl-2-(naphthalen-1-yl)-1,3,2-dioxaborolane | ||||
 |
BD14887 | 188665-74-9 | C13H18BNO3 | 247.10 |
| 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide | ||||