2-(3,4-Dichlorophenyl)malondialdehyde
2-(3,4-Dichlorophenyl)malondialdehyde
CAS: 849936-29-4
Molecular Formula: C9H6Cl2O2
2-(3,4-Dichlorophenyl)malondialdehyde - Names and Identifiers
| Name | 2-(3,4-Dichlorophenyl)malondialdehyde |
| Synonyms | Propanedial, 2-(3,4-dichlorophenyl)- 2-(3,4-Dichlorophenyl)malondialdehyde 2-(3,4-DICHLOROPHENYL)MALONDIALDEHYDE |
| CAS | 849936-29-4 |
2-(3,4-Dichlorophenyl)malondialdehyde - Physico-chemical Properties
| Molecular Formula | C9H6Cl2O2 |
| Molar Mass | 217.05 |
| Melting Point | 167～170℃ |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD02261891 |
2-(3,4-Dichlorophenyl)malondialdehyde - Introduction
2-(3,4-Dichlorophenyl)malondialdehyde is an organic compound whose chemical formula is C10H6Cl2O2. It belongs to the class of aromatic aldehydes containing two carbonyl groups and a 3,4-dichlorophenyl group.
Regarding the properties of 2-(3,4-Dichlorophenyl)malondialdehyde, it is a colorless crystalline solid, stable at room temperature, and has a higher melting point and boiling point. It is poorly soluble in solvents and can be dissolved in some organic solvents, such as dimethyl sulfoxide and dimethyl formamide.
2-(3,4-Dichlorophenyl)malondialdehyde is chemically highly reductive and oxidative. It can be structurally characterized by techniques such as nuclear magnetic resonance. Its properties make it widely used in the field of organic synthesis.
In practical applications, 2-(3,4-Dichlorophenyl)malondialdehyde is used as a fluorescent probe, a DNA cross-linking agent and a precursor of anticancer drugs. It can be used as a dye and labeling reagent in biology and medicinal chemistry. It has important biological activities, so it has been widely concerned in drug research and development.
The process for the preparation of 2-(3,4-Dichlorophenyl)malondialdehyde mainly starts from malonic dianhydride. First, malonic dianhydride reacts with 3,4-dichloroaniline to obtain an intermediate product, and then through a series of chemical reactions and purification steps, the target product 2-(3,4-Dichlorophenyl)malondialdehyde is finally obtained.
Regarding safety information, 2-(3,4-Dichlorophenyl)malondialdehyde is stable under general operating conditions. However, when handling this compound, appropriate precautions should be taken, such as wearing safety gloves and goggles. And should try to avoid inhalation, intake or skin contact. When using this compound, attention should be paid to its possible irritation and toxicity, and waste should be properly disposed. During use, follow the laboratory's safety procedures to ensure safety.
Regarding the properties of 2-(3,4-Dichlorophenyl)malondialdehyde, it is a colorless crystalline solid, stable at room temperature, and has a higher melting point and boiling point. It is poorly soluble in solvents and can be dissolved in some organic solvents, such as dimethyl sulfoxide and dimethyl formamide.
2-(3,4-Dichlorophenyl)malondialdehyde is chemically highly reductive and oxidative. It can be structurally characterized by techniques such as nuclear magnetic resonance. Its properties make it widely used in the field of organic synthesis.
In practical applications, 2-(3,4-Dichlorophenyl)malondialdehyde is used as a fluorescent probe, a DNA cross-linking agent and a precursor of anticancer drugs. It can be used as a dye and labeling reagent in biology and medicinal chemistry. It has important biological activities, so it has been widely concerned in drug research and development.
The process for the preparation of 2-(3,4-Dichlorophenyl)malondialdehyde mainly starts from malonic dianhydride. First, malonic dianhydride reacts with 3,4-dichloroaniline to obtain an intermediate product, and then through a series of chemical reactions and purification steps, the target product 2-(3,4-Dichlorophenyl)malondialdehyde is finally obtained.
Regarding safety information, 2-(3,4-Dichlorophenyl)malondialdehyde is stable under general operating conditions. However, when handling this compound, appropriate precautions should be taken, such as wearing safety gloves and goggles. And should try to avoid inhalation, intake or skin contact. When using this compound, attention should be paid to its possible irritation and toxicity, and waste should be properly disposed. During use, follow the laboratory's safety procedures to ensure safety.
Last Update：2024-04-09 21:01:54
