2-bromo-4-chloropropiophenone
2-bromo-4-chloropropiophenone
CAS: 877-37-2
Molecular Formula: C9H8BrClO
2-bromo-4-chloropropiophenone - Names and Identifiers
| Name | 2-bromo-4-chloropropiophenone |
| Synonyms | 2-bromo-4-chloropropiophenone 2-Bromo-1-(4-chlorophenyl)-1-propanone 1-Propanone, 2-bromo-1-(4-chlorophenyl)- 2-Bromo-1-(4-chloro-phenyl)-propan-1-one, 2-Бром-1-(4-хлорфенил)-пропан-1-он, 2-bromo-4'-chloropropiophenone |
| CAS | 877-37-2 |
| EINECS | 100-413-0 |
2-bromo-4-chloropropiophenone - Physico-chemical Properties
| Molecular Formula | C9H8BrClO |
| Molar Mass | 247.52 |
| Density | 1.518±0.06 g/cm3(Predicted) |
| Melting Point | 77-79 °C(Solv: ligroine (8032-32-4)) |
| Boling Point | 296.7±15.0 °C(Predicted) |
| Storage Condition | Room Temprature |
2-bromo-4-chloropropiophenone - Introduction
It is an organic compound with a molecular formula of C9H8BrClO and a relative molecular mass of 235.52g/mol. It is a colorless to yellowish solid with a pungent odor.
It has a wide range of applications in chemical synthesis. It is often used as an intermediate in the synthesis of other organic compounds, such as heterocyclic compounds, drugs, dyes, etc.
The preparation method is usually obtained by reacting phenylacetone with bromine and chlorine. First, phenylacetone is reacted with sodium hydroxide to form sodium phenylacetone. Then, bromine and chloric acid are added at low temperature, and the target product is obtained by reaction.
Regarding safety information, is an organic compound and should be handled with care. Appropriate personal protective equipment, such as gloves and protective glasses, should be worn during laboratory operations or industrial production to avoid direct contact. In addition, it should be kept away from fire sources and oxidants to avoid fire or explosion. When stored, it should be kept in a dry, cool place and away from combustibles and food. If necessary, use a suitable ventilation system to ensure good ventilation of the work area.
It has a wide range of applications in chemical synthesis. It is often used as an intermediate in the synthesis of other organic compounds, such as heterocyclic compounds, drugs, dyes, etc.
The preparation method is usually obtained by reacting phenylacetone with bromine and chlorine. First, phenylacetone is reacted with sodium hydroxide to form sodium phenylacetone. Then, bromine and chloric acid are added at low temperature, and the target product is obtained by reaction.
Regarding safety information, is an organic compound and should be handled with care. Appropriate personal protective equipment, such as gloves and protective glasses, should be worn during laboratory operations or industrial production to avoid direct contact. In addition, it should be kept away from fire sources and oxidants to avoid fire or explosion. When stored, it should be kept in a dry, cool place and away from combustibles and food. If necessary, use a suitable ventilation system to ensure good ventilation of the work area.
Last Update：2024-04-09 21:01:54
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