Ethanone, 2,2,2-trifluoro-1-(1H-indol-3-yl)- - Names and Identifiers
Ethanone, 2,2,2-trifluoro-1-(1H-indol-3-yl)- - Physico-chemical Properties
Molecular Formula | C10H6F3NO
|
Molar Mass | 213.16 |
Density | 1.423±0.06 g/cm3(Predicted) |
Melting Point | 211-214°C(lit.) |
Boling Point | 308.6±37.0 °C(Predicted) |
Flash Point | 140.4°C |
Vapor Presure | 0.000675mmHg at 25°C |
Appearance | Solid |
Color | White to Almost white |
pKa | 14.31±0.30(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.568 |
MDL | MFCD00182114 |
Ethanone, 2,2,2-trifluoro-1-(1H-indol-3-yl)- - Risk and Safety
Hazard Symbols | Xi - Irritant
|
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin.
|
Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36 - Wear suitable protective clothing.
|
WGK Germany | 3 |
Hazard Class | IRRITANT |
Ethanone, 2,2,2-trifluoro-1-(1H-indol-3-yl)- - Introduction
3-(Trifluoroacetyl)indole is an organic compound with the chemical formula C11H6F3NO. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 3-(Trifluoroacetyl)indole is a white to light yellow solid.
-Solubility: It is soluble in organic solvents such as chloroform, dimethyl sulfoxide and dimethylformamide.
-Melting point: Its melting point is about 110-113 degrees Celsius.
Use:
- 3-(Trifluoroacetyl)indole is an important organic synthesis intermediate that can be used to synthesize various other compounds, such as pharmaceutically active molecules and pesticides.
-It can also be used as a synthetic precursor for dyes, catalysts and optical materials.
Method:
- 3-(Trifluoroacetyl)indole can be obtained by reacting indole with Trifluoroacetyl chloride. A specific step is to react the indole with trifluoroacetyl chloride in a suitable solvent, usually at low temperature, and using a suitable catalyst.
Safety Information:
- 3-(Trifluoroacetyl)indole has limited toxicity and hazard data and should be used in accordance with regular laboratory practices.
-Pay attention to prevent it from contacting with oxygen during handling and storage to avoid fire or explosion.
-Wear personal protective equipment such as glasses and gloves when conducting experiments.
-Detailed safety information should refer to the safety data sheet of the compound.
Last Update:2024-04-09 02:00:42