Boronic acid, B-[6-(1-piperidinyl)-3-pyridinyl]-
6-(Piperidin-1-yl)pyridin-3-ylboronic acid
CAS: 1002129-33-0
Molecular Formula: C10H15BN2O2
Boronic acid, B-[6-(1-piperidinyl)-3-pyridinyl]- - Names and Identifiers
Boronic acid, B-[6-(1-piperidinyl)-3-pyridinyl]- - Physico-chemical Properties
| Molecular Formula | C10H15BN2O2 |
| Molar Mass | 206.05 |
| Storage Condition | 2-8°C |
| Sensitive | Irritant |
| MDL | MFCD06801705 |
Boronic acid, B-[6-(1-piperidinyl)-3-pyridinyl]- - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | 22 - Harmful if swallowed |
| Hazard Class | IRRITANT |
Boronic acid, B-[6-(1-piperidinyl)-3-pyridinyl]- - Introduction
6-(Piperidin-1-yl)pyridin-3-ylboronic acid is an organic boron compound with the chemical formula C11H15BN2O2.
Properties: 6-(Piperidin-1-yl)pyridin-3-ylboronic acid is a white crystalline solid, soluble in some organic solvents such as chloroform and methanol, slightly soluble in water. It is stable in the air.
Purpose: 6-(Piperidin-1-yl)pyridin-3-ylboronic acid is an important reagent in organic synthesis, often used as a ligand to participate in metal-catalyzed reactions. It can be used to synthesize various organic compounds, such as drugs, dyes and polymers.
preparation method: 6-(Piperidin-1-yl)pyridin-3-ylboronic acid can be obtained by substitution reaction of piperidine and pyridine and boration. Specific synthetic methods can refer to the relevant literature and laboratory manuals of organic synthetic chemistry.
Safety information: Pay attention to safe operation when using it, and avoid direct contact with skin and eyes. It should be operated under well-ventilated conditions to prevent inhalation. If exposed or inhaled, seek medical attention promptly.
Properties: 6-(Piperidin-1-yl)pyridin-3-ylboronic acid is a white crystalline solid, soluble in some organic solvents such as chloroform and methanol, slightly soluble in water. It is stable in the air.
Purpose: 6-(Piperidin-1-yl)pyridin-3-ylboronic acid is an important reagent in organic synthesis, often used as a ligand to participate in metal-catalyzed reactions. It can be used to synthesize various organic compounds, such as drugs, dyes and polymers.
preparation method: 6-(Piperidin-1-yl)pyridin-3-ylboronic acid can be obtained by substitution reaction of piperidine and pyridine and boration. Specific synthetic methods can refer to the relevant literature and laboratory manuals of organic synthetic chemistry.
Safety information: Pay attention to safe operation when using it, and avoid direct contact with skin and eyes. It should be operated under well-ventilated conditions to prevent inhalation. If exposed or inhaled, seek medical attention promptly.
Last Update：2024-04-09 19:06:02
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