Benzeneacetyl chloride, 3,5-bis(trifluoromethyl)- - Names and Identifiers
Benzeneacetyl chloride, 3,5-bis(trifluoromethyl)- - Physico-chemical Properties
Molecular Formula | C10H5ClF6O
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Molar Mass | 290.59 |
Density | 1.469±0.06 g/cm3(Predicted) |
Boling Point | 103/10mm |
Benzeneacetyl chloride, 3,5-bis(trifluoromethyl)- - Risk and Safety
Hazard Symbols | C - Corrosive
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Risk Codes | R34 - Causes burns
R41 - Risk of serious damage to eyes
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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.
S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
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Hazard Note | Corrosive |
Benzeneacetyl chloride, 3,5-bis(trifluoromethyl)- - Introduction
3,5-bis (TRIFLUOROMETHYL)PHENYLACETYL CHLORIDE, also known as 3,5-bis (TRIFLUOROMETHYL)PHENYLACETYL CHLORIDE, is an organic compound. It has the chemical formula C9H6ClF6O and has the following properties:
1. Appearance: 3,5-bis (TRIFLUOROMETHYL)PHENYLACETYL CHLORIDE is a colorless to pale yellow liquid with a pungent odor.
2. Solubility: It is almost insoluble in water, but soluble in organic solvents, such as ether, dimethylformamide and chlorinated hydrocarbons.
3. Stability: It is a stable compound that is not easy to decompose at room temperature.
4. Reactivity: 3,5-bis (TRIFLUOROMETHYL)PHENYLACETYL CHLORIDE is a strong acylating agent, which can react with active functional groups such as amino group and hydroxyl group.
This compound is commonly used in organic synthesis, the main uses are as follows:
1. Acylation reagent: Due to its strong acylation reaction properties, 3,5-bis (TRIFLUOROMETHYL)PHENYLACETYL CHLORIDE can be used as an acylation reagent in organic synthesis to introduce acyl groups.
2. Pesticide: The compound has good insecticidal activity and can be used in the agricultural field as an intermediate for pesticides.
3. Pharmaceutical research: It can also be used as an intermediate in pharmaceutical research for the synthesis of drugs.
Regarding the preparation method, the preparation of 3,5-bis (TRIFLUOROMETHYL)PHENYLACETYL CHLORIDE usually adopts a chemical synthesis method. A common preparation method is to react 3,5-difluoroacetophenone with trifluoromethane anhydride under basic conditions to obtain the desired product.
During use and storage, you need to pay attention to its safety information:
1. Toxicity: The compound is an organic compound and may be toxic to the human body. During operation, wear appropriate protective equipment such as gloves and goggles to avoid contact with skin and eyes.
2. Burning and explosion: 3,5-bis (TRIFLUOROMETHYL)PHENYLACETYL CHLORIDE may be flammable liquid. Contact with open flame and high temperature should be avoided to prevent fire and explosion accidents.
3. Storage: The compound should be stored in a cool, ventilated and dry place, away from flammable materials and direct sunlight.
4. Disposal: Disposal shall be carried out in accordance with local laws and regulations to avoid harm to the environment and human body.
Last Update:2024-04-09 21:49:45