Chemical Formula | C7H3F2N |
Molecular Weight | 139.10 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 189 - 190 °C |
Melting Point | N/A |
Density | 1.285 g/cm³ |
Flash Point | 76 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Purity | Typically high - purity commercial products around 98%+ |
Chemical Formula | C7H3F2N |
Molecular Weight | 139.102 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 195 - 197 °C |
Melting Point | N/A |
Density | 1.316 g/cm³ |
Flash Point | 82 °C |
Solubility | Insoluble in water, soluble in organic solvents like ethanol, ether |
Vapor Pressure | N/A |
Refractive Index | 1.505 - 1.507 |
Chemical Formula | C7H3F2N |
Molecular Weight | 139.102 |
Appearance | Liquid (usually) |
Color | Colorless to light yellow |
Odor | Characteristic aromatic odor |
Boiling Point | Around 185 - 187 °C |
Density | Approx. 1.31 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
Flash Point | Approx. 73 °C |
Purity | Typically high - purity products around 98%+ in commercial form |
Stability | Stable under normal conditions, but may react with strong oxidizing agents |
What are the main uses of 5-cyano-1,3-difluorobenzene?
5-Amino-1,3-diethylbenzene is an organic compound and is widely used in the chemical industry. Its main uses are as follows:
First, it is used as a raw material for organic synthesis. It can be obtained through many chemical reactions. Various organic compounds with different functions can be obtained. Such as reacting with specific reagents to form complex intermediates, which lay the foundation for the synthesis of drugs, dyes and fragrances. Taking the synthesis of a new type of drug as an example, 5-amino-1,3-diethylbenzene is the key starting material. After multi-step reactions, the active molecular structure of drugs is constructed, which is of great significance for drug research and development.
Second, it is used for the preparation of polymer materials. With the help of polymerization, it can participate in the synthesis of polymer compounds. Such as copolymerization with other monomers, giving polymer materials special properties, such as improving the heat resistance and mechanical strength of the material. In the preparation of high-performance engineering plastics, the addition of 5-amino-1,3-diethylbenzene can optimize the material properties and broaden its application in aerospace, automobile manufacturing and other fields.
Third, it has made great contributions to the dye industry. It can be used as an important intermediate for synthetic dyes. With its amino and ethylbenzene structures, it imparts specific colors and properties to dye molecules. Synthetic dyes have the advantages of bright color, good light resistance and high dyeing fastness, and are widely used in textile, printing and dyeing industries.
Fourth, it plays a role in the field of medicine. As a key intermediate in the synthesis of some drugs, it participates in the construction of drug molecules and provides the necessary structural basis for drug activity. The synthesis process of some drugs with specific pharmacological activities relies on 5-amino-1,3-diethylbenzene, and a series of reactions are used to obtain drugs with therapeutic efficacy.
What are the physical properties of 5-cyano-1,3-difluorobenzene?
5-Amino-1,3-diethylbenzene is one of the organic compounds. It has many physical properties, and although there is no such specific substance in the traditional process involved in "Tiangong Kaiwu", the way the ancients described the characteristics of the substance may be as follows:
Under the normal condition of this substance, it may be a colorless to light yellow liquid. It has a transparent and clear state, just like dew drops in the morning, slightly glowing under the light. Close to the smell, there is a special aromatic smell, just like a rare flower and tree in the mountains and forests, which is unique and recognizable.
Its boiling point is worth noting. At a certain temperature range, when placed in a specific container and heated with fire, to a certain temperature, it will be seen as smart water, turning into curling hot gas rising. The temperature at this time is the key node of its gasification, just like the ancients controlled the temperature during alchemy, and this boiling point is crucial for its separation, purification and other operations.
The melting point of 5-amino-1,3-diethylbenzene is also its remarkable characteristic. When the external temperature gradually decreases to a certain low temperature, the liquid that originally flowed gradually solidifies, just like the freezing of the lake in winter, spreading from the edge to the center, and finally becoming a solid state. The temperature of this solidification is the melting point, which is like a certain internal scale of a substance, defining the transformation of its solid-liquid form.
As for the density, compared with water, if a small amount of this substance is gently dripped into the water, it can be seen whether it sinks or floats, to judge its relationship with the density of water. If it sinks underwater, it indicates that its density is greater than that of water, just like a stone sinking to the bottom of the water; if it floats on the water surface, the density is less than that of water, such as wood leaves floating on the lake surface.
In terms of solubility, it varies in different solvents. In organic solvents, such as certain alcohols and ethers, they can dissolve in water like salts, disperse rapidly, dissolve, and blend seamlessly with them; while in water, their solubility is poor, and they may only disperse slightly. For example, when oil drops into water, it is difficult to be completely miscible, and only a little cloudy appears.
Is 5-cyano-1,3-difluorobenzene chemically stable?
5-Amino-1,3-diethylbenzene has stable chemical properties at room temperature and pressure. In the molecular structure of this compound, the amino group interacts with the group of diethylbenzene, causing it to exhibit specific chemical properties.
Amino group has certain electron-giving properties and can participate in many chemical reactions. It can react with acid substances to form corresponding salts. Due to the presence of lone pair electrons in the nitrogen atom in the amino group, it is easy to accept protons and form cations when encountering acids.
Furthermore, the structure of 1,3-diethylbenzene endows the compound with certain aromaticity and lipid solubility. The presence of the aromatic ring makes the molecule relatively stable and can participate in the electrophilic substitution reaction. The ethyl group of diethylbenzene is the power supply group, which can increase the electron cloud density of the benzene ring, and is more vulnerable to the attack of electrophilic reagents during the electrophilic substitution reaction.
However, this substance is not absolutely stable. In case of high temperature, open flame or strong oxidant, there may be a risk of violent reaction. High temperature can cause the vibration of chemical bonds in the molecule to intensify. To a certain extent, the chemical bonds may break, causing chemical reactions to occur. Strong oxidants can oxidize with amino or benzene rings, changing the structure and properties of molecules. Under normal storage and use conditions, the chemical properties of 5-amino-1,3-diethylbenzene can be maintained relatively stable as long as it is protected from high temperatures, open flames and strong oxidizing agents, and can be safely used in various chemical synthesis and related fields.
What is the production process of 5-cyano-1,3-difluorobenzene?
For 5-amino-1,3-dibromobenzene, there are various methods for making it. The commonly used method is to first take a suitable benzene substrate, mostly starting with benzene, and through ingenious chemical changes, to form this compound.
Initially, benzene can be interacted with a specific reagent to introduce an amino group. This step often starts with the method of nitrification. The mixed acid phase of benzene and concentrated nitric acid and concentrated sulfuric acid can be combined at a suitable temperature and duration to obtain nitrobenzene. Nitrobenzene has strong reactivity. After the reduction method, metals and acids, such as iron and hydrochloric acid, or catalytic hydrogenation are used to convert nitro groups into amino groups to obtain aniline. < Br >
To obtain aniline, the next step is to introduce bromine atoms. Using aniline as a substrate, react with bromine reagents. Liquid bromine is often used as a bromine source, and an appropriate amount of catalyst, such as iron powder, is added to a suitable solvent, such as glacial acetic acid. Liquid bromine reacts slowly with aniline, and bromine atoms replace hydrogen atoms on the benzene ring one by one. Because the amino group is an ortho and para-site group, bromine atoms are introduced into the ortho and para-sites of the amino group. After fine control of reaction conditions, such as temperature and bromine dosage, 5-amino-1,3-dibromobenzene can be obtained. < Br >
There are other ways to make it, or use the protective group strategy, first protect the amino group with a suitable group to prevent its overreaction, and then remove the protective group after the bromination reaction is completed. In short, the preparation of 5-amino-1,3-dibromobenzene requires making good use of various reactions and fine regulation conditions according to its chemical properties.
What are the precautions for storing and transporting 5-cyano-1,3-difluorobenzene?
5-Amino-1,3-diethylbenzene, when storing and transporting, pay attention to many matters.
It has certain chemical activity, encounters open flames and hot topics, and is very easy to burn. Therefore, the storage place should be kept away from fire and heat sources, keep well ventilated, and should be stored separately from oxidants and acids, and must not be mixed to prevent severe chemical reactions. When transporting, the transportation vehicle should also ensure that there is no leakage and no damage, and it should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment.
Furthermore, 5-amino-1,3-diethylbenzene may pose a potential hazard to human health. Its vapor or fog droplets can irritate the eyes, respiratory tract and skin. Clear warning signs should be set up in storage places to inform personnel of the danger of this chemical. Transportation operators should strictly follow the operating procedures and wear appropriate protective equipment, such as gas masks, protective gloves, protective glasses, etc., to avoid direct contact with the chemical.
In addition, for the storage of 5-amino-1,3-diethylbenzene, there should also be reasonable planning. Do not store in excess, so as to avoid serious consequences in the event of an accident. The storage area should be inspected regularly to check for leaks, damaged packaging, etc. If there is any abnormality, it needs to be dealt with in time. During transportation, close attention should also be paid to the status of the goods to ensure the safety of transportation. The storage and transportation of 5-amino-1,3-diethylbenzene must be treated strictly, and relevant regulations and requirements must be followed to ensure personnel safety, environmental safety, and stable storage and smooth transportation of chemicals.