Chemical Formula | C8H10FN |
Molecular Weight | 139.17 |
Appearance | Typically a colorless to light - yellow liquid |
Boiling Point | Around 190 - 195 °C |
Density | Approx. 1.07 g/cm³ |
Solubility | Soluble in organic solvents like ethanol, diethyl ether |
Flash Point | Ca. 72 °C |
Vapor Pressure | Low at room temperature |
Odor | Characteristic amine - like odor |
Chemical Formula | C8H10FN |
Molar Mass | 139.17 g/mol |
Appearance | Typically a colorless to light - colored liquid |
Boiling Point | Approximately 203 - 205 °C |
Solubility In Water | Low solubility in water, likely hydrophobic as it is an organic compound with non - polar benzene ring |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether, and chloroform |
Pka Of The Amine Group | Estimated around 9 - 10 for the basicity of the amine group |
Chemical Formula | C8H10FN |
Appearance | Typically a liquid |
Odor | Characteristic organic odor |
Boiling Point | Around 189 - 191 °C |
Density | Approx. 1.05 g/cm³ |
Solubility In Water | Poorly soluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Flash Point | Approx. 74 °C |
Stability | Stable under normal conditions, but reactive with strong oxidants |
What are the main uses of 3-Fluoro-benzeneethanamine?
3-Fluoro-benzeneethanamine, Chinese name 3-fluorophenethylamine, is widely used. In the field of medicinal chemistry, it is often used as a key intermediate to synthesize a variety of drugs with special effects. Due to the unique electronic properties and spatial effects of fluorine atoms, after the introduction of 3-fluorophenethylamine structure, the drug may be significantly optimized in terms of biological activity, metabolic stability and target affinity. For example, in the development of neurological drugs, compounds containing 3-fluorophenethylamine structure may better penetrate the blood-brain barrier and act on neurological targets, providing a potential effective way for the treatment of neurodegenerative diseases, psychiatric diseases, etc.
In the field of materials science, 3-fluorophenethylamine may participate in the preparation of special functional materials. Due to the presence of amino groups and benzene rings in its structure, it can chemically react with a variety of compounds to form polymers or composites with unique properties. Such materials may exhibit special properties in optics, electricity, magnetism, etc., and are used in the manufacture of new electronic devices, optical materials, etc.
In the field of organic synthesis chemistry, 3-fluorophenethylamine, as an important building block for organic synthesis, can participate in many classical organic reactions, such as nucleophilic substitution and coupling reactions, by virtue of the activity of fluorine atoms on amino and benzene rings. It provides an effective method for constructing complex organic molecular structures, and helps to synthesize organic compounds with diverse structures and specific functions, promoting the development of organic synthesis chemistry.
What are the physical properties of 3-Fluoro-benzeneethanamine?
3-Fluoro-phenethylamine is a genus of organic compounds. Its physical properties are worth exploring.
Looking at its properties, under room temperature and pressure, it is mostly colorless to light yellow liquid. The characteristics of this color state can help to distinguish between objects. And smell, or have a special smell, although it is difficult to describe exactly, it is also one of its characteristics.
When it comes to the melting point, the melting point value is low, and it does not appear solid at room temperature, which is due to the characteristics of intermolecular forces. The boiling point is relatively moderate, but the exact value will vary depending on the change of environmental pressure. Usually at standard atmospheric pressure, the boiling point is maintained within a certain range, so that the phase state of this substance can be converted within a specific temperature range.
In terms of solubility, 3-fluoro-phenethylamine exhibits good solubility in organic solvents such as ethanol and ether. This is due to the principle of similarity and compatibility, and its molecular structure is compatible with the molecules of organic solvents, so it can be miscible with each other. In water, the solubility is relatively limited, because the molecular polarity matches the polarity of water molecules imperfectly.
Density is also the key to physical properties. Compared with water, its density may vary, generally slightly greater than water, so if mixed with water, after standing, or see the appearance of stratification, this material sinks to the bottom of the water.
In addition, 3-fluoro-phenethylamine has a certain volatility and can slowly dissipate in the air. This characteristic also affects its storage and use conditions. It needs to be properly sealed to prevent its volatilization loss. And because it is an organic amine, or has irritating effects on the skin, eyes, respiratory tract, etc., when operating, be careful and follow safety procedures.
What is the chemistry of 3-Fluoro-benzeneethanamine?
3 - Fluoro - benzeneethanamine, an organic compound, is an amine derivative. Looking at its chemical properties, fluorine atoms and phenethylamine structures give it unique properties.
Let's talk about fluorine atoms first. Its electronegativity is quite high. After introducing into the molecule, it will cause the distribution of electron clouds to change and enhance the polarity of the molecule. This polarity change has a great impact on the physical and chemical properties of the compound. For example, in terms of solubility, the solubility in polar solvents may be improved due to the increase in polarity. And the special electronic effects of fluorine atoms will affect the electron density of the benzene ring, changing the activity and selectivity of the electrophilic substitution reaction on the benzene ring. Usually, it will reduce the electron cloud density of the benzene ring, making the electrophilic substitution reaction more difficult and the reaction conditions more severe.
Looking at the structure of phenethylamine, this structure gives the compound a certain alkalinity. The lone pair electrons on the nitrogen atom can bind protons and appear alkaline. However, its alkalinity is affected by the surrounding substituents. In 3-Fluoro-benzeneethanamine, the electron-absorbing action of the fluorine atom or the electron cloud density of the nitrogen atom decreases, which weakens the alkalinity. At the same time, the structure of phenethylamine makes the compound have a certain nucleophilicity, and the lone pair electrons of the nitrogen atom can attack the electrophilic reagents and participate in the nucleophilic substitution or addition reaction.
In addition, the compound has aromatic properties due to its benzene ring, and can undergo typical reactions such as halogenation, nitrification, and sulfonation of benzene rings However, due to the presence of fluorine atoms, the specific reaction conditions and product distribution or reaction with benzene itself are different. In short, 3-Fluoro-benzeneethanamine exhibits unique and complex chemical properties due to the interaction of fluorine atoms and phenethylamine structures, which is of important research and application value in the fields of organic synthesis and medicinal chemistry.
What are 3-Fluoro-benzeneethanamine synthesis methods?
The synthesis of 3-fluoro-phenethylamine is a key topic in organic synthetic chemistry. This compound has important uses in many fields such as medicine and pesticides. Although the synthesis methods contained in ancient books are different from today's science, there are also lessons to be learned.
The method of the past may start with fluorobenzene derivatives. First take fluorobenzene, and react with halogenated alkanes with suitable halogenated reagents, such as ferric halides, to obtain halogenated fluorobenzene. This step requires controlling the reaction conditions so that the halogen atom is precisely replaced in a specific position of the benzene ring to meet the structural requirements of the target product.
Then, the halogenated fluorobenzene is reacted with magnesium to form a Grignard reagent. This Grignard reagent is highly active and can react with alcaldes or ketones to introduce carbon-containing chain fragments. For example, it reacts with acetaldehyde to generate the corresponding alcohol.
Furthermore, the obtained alcohol is converted into aldehyde by suitable oxidation means, such as mild oxidizing agents. Subsequently, the aldehyde is reacted with ammonia or amine compounds by reductive amination, and in the presence of suitable reducing agents, 3-fluoro-phenethylamine can be obtained. In this process, the control of reaction conditions at each step is extremely important, such as temperature, pH, reaction time, etc., all of which are related to the purity and yield of the product. < Br >
There are also other methods, which can be started from fluorinated styrene. First, fluorinated styrene is added to hydrogen halide to obtain halogenated phenethane derivatives. Then through nucleophilic substitution reaction, the halogen atom is replaced by an amine reagent, and then 3-fluoro-phenethylamine is obtained. The steps of this approach may be slightly simpler, but attention should also be paid to the selectivity of each step of the reaction and the control of side reactions.
There are many methods for synthesizing 3-fluoro-phenethylamine, but all of them need to be finely regulated. According to actual needs and conditions, the most suitable method should be selected to achieve the purpose of efficient and high-purity synthesis.
What is the price range of 3-Fluoro-benzeneethanamine in the market?
I look at your question, but I am inquiring about the price range of 3 - Fluoro - benzeneethanamine in the market. However, this is not an easy question to answer, and its price fluctuates quite a lot and is influenced by many factors.
First, the purity is deeply affected. If the purity is extremely high and almost perfect, the price will be high; on the contrary, if there are more impurities and the purity is slightly lower, the price will be slightly cheaper. For high purity, the price per gram may reach tens to hundreds of yuan; if the purity is slightly lower, it may be reduced to several yuan per gram.
Second, the market supply and demand situation is also the key. If there are many people who want it, the supply will exceed the demand, and the price will rise; if there is an excess supply, no one will pay attention, and the price will fall.
Third, the cost of raw materials and the difficulty of preparation both play a role. Preparation is difficult, raw materials are scarce and expensive, the cost is greatly increased, and its price in the market is also high.
Fourth, the differences in sales channels and regions cannot be ignored. Regular large pharmaceutical companies or suppliers, due to strict quality control and comprehensive service, the price may be high; while small channels and underdeveloped areas, the price may be slightly lower.
Overall, if it is a common commercial grade purity, the price per gram may be between a few yuan and tens of yuan; if it is a scientific research grade high purity, it may be over 100 yuan per gram. However, this is only a rough estimate, and the actual price should be subject to real-time market conditions.