5-Pyrimidineacetaldehyde, 4,6-dichloro-2-methyl-
2-(4,6-Dichloro-2-methylpyrimidin-5-yl)-acetaldehyde
CAS: 474656-37-6
Molecular Formula: C7H6Cl2N2O
5-Pyrimidineacetaldehyde, 4,6-dichloro-2-methyl- - Names and Identifiers
5-Pyrimidineacetaldehyde, 4,6-dichloro-2-methyl- - Physico-chemical Properties
| Molecular Formula | C7H6Cl2N2O |
| Molar Mass | 205.04 |
| Density | 1.402±0.06 g/cm3(Predicted) |
| Boling Point | 304.2±37.0 °C(Predicted) |
| pKa | -4.03±0.39(Predicted) |
| Storage Condition | -20℃ |
| Sensitive | IRRITANT |
| MDL | MFCD19105244 |
5-Pyrimidineacetaldehyde, 4,6-dichloro-2-methyl- - Risk and Safety
| Hazard Class | IRRITANT |
5-Pyrimidineacetaldehyde, 4,6-dichloro-2-methyl- - Introduction
2-(4,-acetaldehyde) is an organic compound with the formula C8H7Cl2N3O. It is a colorless to pale yellow solid.
2-(4,)-acetaldehyde is often used as an insecticide. It has the ability to kill pests such as the leaf roller moth and is often used to protect crops and fruit trees. In addition, it can also be used to synthesize other organic compounds, such as fluorescent dyes, pharmaceutical intermediates, etc.
The method of preparing 2-(4,)-acetaldehyde generally adopts the method of chemical synthesis. A common preparation method is to react 4,6-dichloro-2-methylpyridine with ethyl acetoacetate under alkaline conditions to produce the alcohol ether corresponding to ethyl acetate, which is then hydrolyzed under acidic conditions to obtain the target compound.
Regarding safety information, 2-(4)-acetaldehyde has not yet conducted a comprehensive assessment of the impact on humans and the environment. However, as an organic compound, it needs to be handled and stored to avoid contact with skin and eyes, and to avoid inhalation and ingestion. Appropriate personal protective measures should be taken during use, such as wearing chemical safety glasses, gloves and protective clothing. In case of accidental contact or inhalation, please seek medical attention.
2-(4,)-acetaldehyde is often used as an insecticide. It has the ability to kill pests such as the leaf roller moth and is often used to protect crops and fruit trees. In addition, it can also be used to synthesize other organic compounds, such as fluorescent dyes, pharmaceutical intermediates, etc.
The method of preparing 2-(4,)-acetaldehyde generally adopts the method of chemical synthesis. A common preparation method is to react 4,6-dichloro-2-methylpyridine with ethyl acetoacetate under alkaline conditions to produce the alcohol ether corresponding to ethyl acetate, which is then hydrolyzed under acidic conditions to obtain the target compound.
Regarding safety information, 2-(4)-acetaldehyde has not yet conducted a comprehensive assessment of the impact on humans and the environment. However, as an organic compound, it needs to be handled and stored to avoid contact with skin and eyes, and to avoid inhalation and ingestion. Appropriate personal protective measures should be taken during use, such as wearing chemical safety glasses, gloves and protective clothing. In case of accidental contact or inhalation, please seek medical attention.
Last Update：2024-04-09 20:02:46
