Chemical Formula | C10H12BrF |
Molecular Weight | 233.105 |
Appearance | Typically a colorless to light - yellow liquid |
Boiling Point | Around 220 - 230 °C |
Density | Approx. 1.3 - 1.4 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
Flash Point | Caution: Flammable, flash point around 90 - 100 °C |
Vapor Pressure | Low vapor pressure at room temperature |
Logp | High logP value, indicating lipophilicity |
Chemical Formula | C10H12BrF |
Molar Mass | 233.105 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | Around 220 - 230 °C |
Density | Approx. 1.3 - 1.4 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
Flash Point | Likely above 100 °C |
Vapor Pressure | Low at room temperature |
Name | 2-Bromo-4-t-butyl-1-fluorobenzene |
Chemical Formula | C10H12BrF |
Molar Mass | 231.105 g/mol |
Appearance | Colorless to light yellow liquid |
Density | 1.296 g/mL at 25 °C |
Boiling Point | 209 - 210 °C |
Flash Point | 86.7 °C |
Solubility | Insoluble in water, soluble in organic solvents like ethanol, ether |
Vapor Pressure | Low, as it is a relatively high - boiling liquid |
Stability | Stable under normal conditions, but may react with strong oxidizing agents |
What are the main uses of 2-Bromo-4-t-butyl-1-fluorobenzene?
2-Bromo-4-tert-butyl-1-fluorobenzene is an organic compound with a wide range of uses. In the field of organic synthesis, it is often used as a key intermediate.
The bromine, fluorine and tert-butyl atoms in the genome molecule have unique reactivity and can participate in various organic reactions. Bromine atoms can undergo nucleophilic substitution reactions, such as interacting with nucleophiles such as alcohols and amines, to form novel carbon-oxygen and carbon-nitrogen bonds, thereby constructing more complex organic molecular structures. The introduction of fluorine atoms can significantly change the physical and chemical properties of compounds, such as improving their fat solubility and stability. In the field of medicinal chemistry, this is helpful for the development of drug molecules with specific physiological activities. The steric resistance of tert-butyl is relatively large, which can affect the spatial configuration of molecules, which in turn affects their reaction selectivity.
In the field of materials science, 2-bromo-4-tert-butyl-1-fluorobenzene is also used. Through appropriate chemical reactions, it can be integrated into the structure of polymers, which can endow materials with unique properties, such as improved solubility, thermal stability, and optical properties of materials. For example, when preparing special functional polymer films and coating materials, this compound may play an important role in enabling the material to meet the stringent performance requirements in specific application scenarios.
In summary, 2-bromo-4-tert-butyl-1-fluorobenzene has shown important application value in the fields of organic synthesis and materials science. With its unique molecular structure characteristics, it provides a key material basis for research and production in many fields.
What are the physical properties of 2-Bromo-4-t-butyl-1-fluorobenzene?
2-Bromo-4-tert-butyl-1-fluorobenzene is one of the organic compounds. Its physical properties are quite impressive.
Looking at its properties, under normal temperature and pressure, it is mostly liquid, but it may vary depending on the specific environmental conditions. Its color is colorless or very light, and its appearance is clear, like clear water.
When it comes to boiling point, the boiling point of this compound is in a specific range due to the interaction of atoms and groups in the molecular structure. The existence of bromine, fluorine atoms and tert-butyl groups makes the intermolecular forces different, so the boiling point is different from that of ordinary benzene derivatives. Roughly speaking, the boiling point of benzene is slightly higher than that of benzene due to the heavier atoms and large tert-butyl in its structure. The melting point of
is also closely related to the molecular structure. The symmetry of the molecule, the bonding mode between atoms and the spatial arrangement of the groups all affect its melting point. The molecular structure of 2-bromo-4-tert-butyl-1-fluorobenzene causes its melting point to be at a certain value. This value is the inherent characteristic of the substance and can be used for identification and separation.
As for the density, due to the combination of atomic types and quantities, it is higher than that of water. The relative atomic mass of the bromine atom in its molecule is quite large, and the influence of the fluorine atom and tert-butyl group makes the overall density greater than that of water. In the phenomenon of liquid stratification, it is often in the lower layer.
In terms of solubility, 2-bromo-4-tert-butyl-1-fluorobenzene is an organic compound. According to the principle of similar compatibility, it has good solubility in organic solvents such as ethanol, ether, dichloromethane, etc. In water, because it is a non-polar or weakly polar molecule, it has a significant difference in polarity from water molecules, so its solubility is very small.
Vapor pressure is also one of its important physical properties. At a given temperature, the tendency of molecules to escape from the liquid phase to the gas phase determines the vapor pressure. The vapor pressure of 2-bromo-4-tert-butyl-1-fluorobenzene is restricted by temperature and intermolecular forces, and the temperature increases and the vapor pressure increases.
In summary, the physical properties of 2-bromo-4-tert-butyl-1-fluorobenzene are determined by its molecular structure. It is of great significance in organic synthesis, analytical chemistry and other fields, and can provide a basic basis for related operations and research.
What are 2-Bromo-4-t-butyl-1-fluorobenzene synthesis methods?
To prepare 2-bromo-4-tert-butyl-1-fluorobenzene, the method of organic synthesis is often followed.
First, it can be started from compounds containing benzene rings. If p-tert-butylphenol is used as raw material, the following steps are taken:
First, the hydroxyl group of p-tert-butylphenol is converted into a fluorine atom with hydrofluoric acid. In this step, suitable reaction conditions and catalysts are selected to make the phenolic hydroxyl group react with hydrofluoric acid at a specific temperature and pressure. After the nucleophilic substitution process, the oxygen atom of the phenolic hydroxyl group is attacked by fluoride ions to form p-tert-butylfluorobenzene. The key to this step is to control the reaction temperature and the amount of hydrofluoric acid < Br > Then, p-tert-butyl fluorobenzene and bromine are catalyzed by an appropriate catalyst such as iron or iron salt to undergo electrophilic substitution reaction. Bromine positive ions are attracted by the electron cloud of the benzene ring and attack the benzene ring. According to the positioning rules, because tert-butyl is an ortho-para-localization group, the fluorine atom also has a certain localization effect, and finally the ortho-position is introduced into the bromine atom, so 2-bromo-4-tert-butyl-1-fluorobenzene is obtained. This step should pay attention to the amount of bromine and the reaction time to prevent the formation of polybrominated products.
Second, p-fluorobenzyl ether can also be used as the starting material. First, the tert-butyl chloride and anhydrous aluminum trichloride were used as catalysts to carry out the Fu-gram alkylation reaction, and the tert-butyl group was introduced into the benzene ring para-position to obtain 4-tert-butyl-1-fluorobenzyl ether. This reaction needs to be carried out in an anhydrous environment to ensure the activity of the catalyst.
Then, 4-tert-butyl-1-fluorobenzyl ether was treated with hydrobromic acid to convert the methoxy group into a bromine atom. After the nucleophilic substitution reaction, 2-bromo-4-tert-butyl-1-fluorobenzene was finally obtained. This step requires controlling the concentration of hydrobromic acid and the reaction temperature to make the reaction proceed smoothly.
All synthesis methods require fine regulation of reaction conditions, taking into account factors such as the selection of raw materials, the amount of reagents, the activity of catalysts, and the temperature and time of the reaction, in order to effectively improve the yield and purity of the target product.
2-Bromo-4-t-butyl-1-fluorobenzene what are the precautions during storage and transportation?
2-Bromo-4-tert-butyl-1-fluorobenzene is an organic compound. When storing and transporting, many points need to be paid careful attention.
Bear the brunt of storage. This compound should be stored in a cool, dry and well-ventilated place. Because it is quite sensitive to heat, high temperature can easily decompose or cause other chemical reactions, so it is necessary to keep away from heat and fire sources, such as heating pipes, open flames, etc. Humidity cannot be ignored. Humid environment may deteriorate the compound, so the storage area must be kept dry.
Furthermore, make sure that the container is well sealed when storing. 2-Bromo-4-tert-butyl-1-fluorobenzene may react with oxygen, moisture and other components in the air. A sealed container can effectively prevent such reactions from occurring. After taking it, the container should be sealed immediately.
In terms of transportation, the packaging must be solid and reliable. According to its characteristics, select suitable packaging materials, such as containers with certain pressure and impact resistance, to prevent the leakage of compounds due to package damage during transportation. At the same time, the packaging should be clearly marked with warning labels, indicating its chemical properties and potential hazards, such as toxic and flammable.
During transportation, temperature and vibration must also be strictly controlled. Avoid large fluctuations in temperature and prevent the stability of compounds from being affected by temperature problems. The driving process should be as smooth as possible to reduce vibration and bumps to prevent the compound from causing accidents due to excessive vibration.
In addition, transportation and storage personnel must be professionally trained to be familiar with the characteristics of 2-bromo-4-tert-butyl-1-fluorobenzene and emergency treatment methods. In the event of an emergency such as a leak, they can respond quickly and correctly to reduce the harm.
Only by strictly following the above storage and transportation precautions can we ensure the safety and stability of 2-bromo-4-tert-butyl-1-fluorobenzene during storage and transportation.
What are the effects of 2-Bromo-4-t-butyl-1-fluorobenzene on the environment and human health?
2-Bromo-4-tert-butyl-1-fluorobenzene is one of the organic compounds. In today's world, the relationship between chemicals and the environment and human health has attracted much attention, and this compound is no exception.
On its impact on the environment, the first look at its chemical properties. 2-Bromo-4-tert-butyl-1-fluorobenzene has certain stability and is not easy to decompose rapidly in the natural environment. If released into the environment, or retained in soil and water for a long time. In the soil, due to its hydrophobicity, or adsorption on the surface of soil particles, it hinders the normal exchange and circulation of substances in the soil, affects the absorption of nutrients by plant roots, and thus disturbs the growth of vegetation. In water bodies, it may cause water pollution and endanger aquatic organisms. If aquatic organisms ingest the substance, or due to bioaccumulation, the concentration in the organism gradually increases. Small fish accidentally eat plankton containing this compound, and large fish eat small fish, so accumulated layer by layer, and eventually the content of this substance in the organisms at the top of the food chain is extremely high, destroying the balance of aquatic ecosystems.
As for the impact on human health, it cannot be ignored. If this compound enters the human body through respiration, diet or skin contact, it may endanger human functions. Because it contains halogen atoms, it may interfere with the normal physiological and biochemical reactions of the human body. The existence of bromine and fluorine atoms may make the compound fat-soluble to a certain extent, easily penetrate the cell membrane, and then interfere with important physiological processes such as signal transduction and enzyme activity in the cell. Long-term exposure to this compound environment may increase the risk of cancer in the human body. Halogenated aromatic hydrocarbons are often carcinogenic, and the structure of 2-bromo-4-tert-butyl-1-fluorobenzene is similar to it, or it may be a potential carcinogenic hazard. And it may damage the human nervous system, affect the transmission of neurotransmitters, and cause symptoms such as headache, dizziness, and memory loss.
In summary, 2-bromo-4-tert-butyl-1-fluorobenzene poses a potential threat to the environment and human health, and should be strictly controlled during its production, use, and disposal to protect the ecological environment and human health.