386704-12-7
6-(trifluoromethyl)pyridine-3-carboxaldehyde
CAS: 386704-12-7
Molecular Formula: C7H4F3NO
386704-12-7 - Names and Identifiers
386704-12-7 - Physico-chemical Properties
| Molecular Formula | C7H4F3NO |
| Molar Mass | 175.11 |
| Density | 1.369±0.06 g/cm3(Predicted) |
| Melting Point | 52-56 °C |
| Boling Point | 72 °C |
| Flash Point | 93°C |
| Vapor Presure | 0.252mmHg at 25°C |
| Appearance | Solid |
| pKa | -1.25±0.22(Predicted) |
| Storage Condition | 2-8°C |
| Sensitive | Air Sensitive |
| Refractive Index | 1.476 |
| MDL | MFCD01862647 |
| Physical and Chemical Properties | Melting point 53°C boiling point 72°C flash point 93°C |
386704-12-7 - Risk and Safety
| Risk Codes | R36/37/38 - Irritating to eyes, respiratory system and skin. R43 - May cause sensitization by skin contact R25 - Toxic if swallowed |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection. S36/37 - Wear suitable protective clothing and gloves. S28 - After contact with skin, wash immediately with plenty of soap-suds. |
| UN IDs | UN 2811 6.1/PG 3 |
| WGK Germany | 3 |
| Hazard Note | Irritant |
| Hazard Class | 6.1 |
| Packing Group | Ⅲ |
386704-12-7 - Introduction
6-(trifluoromethyl)pyridine-3-carboxaldehyde is an organic compound with the chemical formula C7H4F3NO. It has a colorless to light yellow liquid with a special benzene ring and pyridine ring structure.
6-(trifluoromethyl)pyridine-3-carboxaldehyde is commonly used as an intermediate in organic synthesis and is widely used in the synthesis of drugs and pesticides. It can be used to synthesize compounds containing trifluoromethyl groups, which generally have good biological activity and antioxidant capacity.
The method for preparing 6-(trifluoromethyl)pyridine-3-carboxaldehyde is mainly to prepare 3-aminopyridine from pyridine, and then react it with trifluoromethyl anhydride to generate 6-(trifluoromethyl)pyridin -3-amine, which is then oxidized to the corresponding aldehyde.
When using safely, it should be noted that the compound is irritating and corrosive, and avoid contact with skin and eyes. Wear appropriate protective equipment such as gloves and goggles during operation. In addition, it should be operated in a well-ventilated place to avoid inhaling its vapors. It is best to store it in a sealed container, away from fire and oxidizing agents.
6-(trifluoromethyl)pyridine-3-carboxaldehyde is commonly used as an intermediate in organic synthesis and is widely used in the synthesis of drugs and pesticides. It can be used to synthesize compounds containing trifluoromethyl groups, which generally have good biological activity and antioxidant capacity.
The method for preparing 6-(trifluoromethyl)pyridine-3-carboxaldehyde is mainly to prepare 3-aminopyridine from pyridine, and then react it with trifluoromethyl anhydride to generate 6-(trifluoromethyl)pyridin -3-amine, which is then oxidized to the corresponding aldehyde.
When using safely, it should be noted that the compound is irritating and corrosive, and avoid contact with skin and eyes. Wear appropriate protective equipment such as gloves and goggles during operation. In addition, it should be operated in a well-ventilated place to avoid inhaling its vapors. It is best to store it in a sealed container, away from fire and oxidizing agents.
Last Update：2024-04-09 21:32:40
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View History
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