1,3-Butanedione, 1-(3-bromophenyl)-4,4,4-trifluoro-
1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione
CAS: 23975-64-6
Molecular Formula: C10H6BrF3O2
1,3-Butanedione, 1-(3-bromophenyl)-4,4,4-trifluoro- - Names and Identifiers
| Name | 1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione |
| Synonyms | LogP 1-(3-BROMOPHENYL)-4,4,4-TRIFLUOROBUTANE-1,3-DIONE 4,4,4-Trifluoro-1-(3-bromophenyl)-1,3-butanedione 1-(3-Bromophenyl)-4,4,4-trifluorobutane-1,3-dione 1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione 1,3-Butanedione, 1-(3-bromophenyl)-4,4,4-trifluoro- |
| CAS | 23975-64-6 |
| InChI | InChI=1/C10H6BrF3O2/c11-7-3-1-2-6(4-7)8(15)5-9(16)10(12,13)14/h1-4H,5H2 |
1,3-Butanedione, 1-(3-bromophenyl)-4,4,4-trifluoro- - Physico-chemical Properties
| Molecular Formula | C10H6BrF3O2 |
| Molar Mass | 295.05 |
| Density | 1.606±0.06 g/cm3(Predicted) |
| Melting Point | 45-47°C |
| Boling Point | 307.8±42.0 °C(Predicted) |
| Flash Point | 139.9°C |
| Vapor Presure | 0.000709mmHg at 25°C |
| pKa | 5.09±0.23(Predicted) |
| Refractive Index | 1.496 |
1,3-Butanedione, 1-(3-bromophenyl)-4,4,4-trifluoro- - Introduction
1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione, also known as 1-(3-bromophenyl)-4,4, 4-trifluoro-butanedione, it is an organic compound. Its chemical formula is C10H5BrF3O2.
This compound has the following properties:
-Appearance: 1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione is a colorless to light yellow crystalline solid.
-Melting point: Its melting point range is 55-60 degrees Celsius.
-Solubility: It is soluble in some organic solvents, such as ethers and ketones.
1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione has some applications in organic synthesis:
-It can be used to synthesize organic fluorescent dyes and fluorescent markers.
-Due to its special chemical structure, it can also be used as a catalyst or ligand in organic synthesis.
The method for preparing 1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione is as follows:
First, bromophenyl ethanone is reacted with fluorinated tetrahydrofuran and Iodoform to obtain 3-bromophenyl ethanone. Then, 3-bromophenyl ethyl ketone was reacted with trifluoroethyl ketone to form the target product 1-(3-bromophenyl)-4,4, 4-trifluororo-butane-1, 3-dione by the process of keto-enol isomerization.
Regarding safety information, according to the laboratory's safety operation procedures, the following precautions should be followed when using:
-This compound may be irritating to the eyes and skin and should be avoided.
-During operation, maintain good ventilation and wear appropriate protective equipment.
-Avoid contact with oxidizing agents during storage and handling.
-Obtain detailed safety information from the supplier regarding the use and handling of this compound, and strictly follow its recommendations.
This compound has the following properties:
-Appearance: 1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione is a colorless to light yellow crystalline solid.
-Melting point: Its melting point range is 55-60 degrees Celsius.
-Solubility: It is soluble in some organic solvents, such as ethers and ketones.
1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione has some applications in organic synthesis:
-It can be used to synthesize organic fluorescent dyes and fluorescent markers.
-Due to its special chemical structure, it can also be used as a catalyst or ligand in organic synthesis.
The method for preparing 1-(3-bromophenyl)-4,4,4-trifluoro-butane-1,3-dione is as follows:
First, bromophenyl ethanone is reacted with fluorinated tetrahydrofuran and Iodoform to obtain 3-bromophenyl ethanone. Then, 3-bromophenyl ethyl ketone was reacted with trifluoroethyl ketone to form the target product 1-(3-bromophenyl)-4,4, 4-trifluororo-butane-1, 3-dione by the process of keto-enol isomerization.
Regarding safety information, according to the laboratory's safety operation procedures, the following precautions should be followed when using:
-This compound may be irritating to the eyes and skin and should be avoided.
-During operation, maintain good ventilation and wear appropriate protective equipment.
-Avoid contact with oxidizing agents during storage and handling.
-Obtain detailed safety information from the supplier regarding the use and handling of this compound, and strictly follow its recommendations.
Last Update：2024-04-10 22:29:15
