12288-74-3
1,1'-Ferrocenedicarbonyl dichloride
CAS: 12288-74-3
Molecular Formula: C12Cl2FeO2
12288-74-3 - Names and Identifiers
| Name | 1,1'-Ferrocenedicarbonyl dichloride |
| Synonyms | Ferrocene,1,1'-bis(chlorocarbonyl)- 1,1'-Ferrocenedicarbonyl dichloride Ferrocene, 1,1'-bis(chlorocarbonyl)- |
| CAS | 12288-74-3 |
12288-74-3 - Physico-chemical Properties
| Molecular Formula | C12Cl2FeO2 |
| Molar Mass | 302.88 |
| Melting Point | 114.0-114.6 °C |
12288-74-3 - Introduction
1,1 '-Ferrocenyl dichloride is an organic compound with the formula [Fe(C5H4)(CO)2Cl]. It is a dark reddish brown crystal, soluble in organic solvents such as dimethylformamide and diethyl ether.
Among them, 1,1 '-ferrocene refers to the structure of two metallocene groups connected together, and metallocene is an aromatic ring composed of five carbon atoms and five hydrogen atoms. The conjugated double bond in the metallocene group gives the compound special electronic properties.
1,1 '-Ferrocenyl dichloride is widely used in organic synthesis. It can be used as a reagent in organic synthesis, usually for introducing iron atoms or metallocene groups into organic compounds. In addition, it can also be used to prepare thioethers and aldehydes and ketones, and play a role in the catalyst.
The method for preparing 1,1 '-ferrocenyl dichloride is generally obtained by reacting 1,1'-ferrocene with carbonitrile chloride. The specific reaction conditions can be adjusted according to the experimental requirements.
Regarding safety information, 1,1 '-Ferrocenyl dichloride is an irritating compound and should be used with caution. During operation, wear protective glasses and gloves to maintain a well-ventilated environment. Avoid contact with the skin and inhalation of dust, such as accidental contact, should immediately wash the affected area with plenty of water. In addition, laboratory safety regulations should be observed and stored in a dry, dark place, away from flammable materials and oxidants.
Among them, 1,1 '-ferrocene refers to the structure of two metallocene groups connected together, and metallocene is an aromatic ring composed of five carbon atoms and five hydrogen atoms. The conjugated double bond in the metallocene group gives the compound special electronic properties.
1,1 '-Ferrocenyl dichloride is widely used in organic synthesis. It can be used as a reagent in organic synthesis, usually for introducing iron atoms or metallocene groups into organic compounds. In addition, it can also be used to prepare thioethers and aldehydes and ketones, and play a role in the catalyst.
The method for preparing 1,1 '-ferrocenyl dichloride is generally obtained by reacting 1,1'-ferrocene with carbonitrile chloride. The specific reaction conditions can be adjusted according to the experimental requirements.
Regarding safety information, 1,1 '-Ferrocenyl dichloride is an irritating compound and should be used with caution. During operation, wear protective glasses and gloves to maintain a well-ventilated environment. Avoid contact with the skin and inhalation of dust, such as accidental contact, should immediately wash the affected area with plenty of water. In addition, laboratory safety regulations should be observed and stored in a dry, dark place, away from flammable materials and oxidants.
Last Update：2024-04-10 22:29:15
