2 Fluoro 6 Iodobenzonitrile
Iodobenzene

2 Fluoro 6 Iodobenzonitrile

Fengxi Chemical

Specifications

HS Code

923984

Chemical Formula C7H3FIN
Appearance Solid (Typical)
Solubility In Water Insoluble (Aromatic nitrile and halogen - containing compound, hydrophobic nature)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (Aromatic and non - polar nature)
Vapor Pressure Very low (Solid at room temperature, non - volatile)
Chemical Formula C7H3FIN
Molecular Weight 251.01
Appearance Solid (Typical description, actual may vary)
Solubility In Water Low (Aromatic nitriles generally have low water solubility)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (Typical for aromatic compounds)
Chemical Formula C7H3FIN
Appearance Solid (likely, based on similar compounds)
Physical State At Room Temp Solid
Solubility In Water Low solubility, as it is an organic nitrile with fluorine and iodine
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Purity Typically Can be high - purity grades available in lab settings, e.g., 95%+
Odor Odor likely pungent and characteristic of nitriles
Chemical Formula C7H3FIN
Molecular Weight 249.01
Appearance Typically a solid (appearance can vary based on purity and conditions)
Melting Point Data may vary, specific value needs further research
Boiling Point Data may vary, specific value needs further research
Density Data may vary, specific value needs further research
Solubility Solubility characteristics in common solvents like organic solvents (e.g., dichloromethane, toluene) need further study
Purity Can be produced in different purity levels depending on synthesis and purification methods
Stability May be sensitive to light, heat, and certain reactive substances
Hazard Class Requires handling with appropriate safety precautions due to halogen content
Packing & Storage
Packing 250g of 2 - fluoro - 6 - iodobenzonitrile in a sealed, chemical - resistant bottle.
Storage 2 - fluoro - 6 - iodobenzonitrile should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly closed container to prevent exposure to air and moisture, which could potentially cause degradation. Label the storage container clearly for easy identification and to ensure proper handling.
Shipping 2 - fluoro - 6 - iodobenzonitrile is shipped in well - sealed, corrosion - resistant containers. It adheres to strict chemical shipping regulations, ensuring proper handling and transportation to prevent any leakage or safety hazards.
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2-fluoro-6-iodobenzonitrile 2-fluoro-6-iodobenzonitrile 2-fluoro-6-iodobenzonitrile
General Information
Frequently Asked Questions
What are the chemical properties of 2-fluoro-6-iodobenzonitrile?
2-Fluoro-6-iodobenzonitrile is a kind of organic compound. Its physical properties, at room temperature, are mostly solid, with specific melting points and boiling points. Due to its rich structure of fluorine, iodine and cyanyl functional groups, its chemical properties are unique.
Fluorine atoms have high electronegativity, which can change the density distribution of the electron cloud of the benzene ring, which in turn affects the reactivity of the molecule. In the electrophilic substitution reaction, the electron cloud density of the adjacent and para-site of the fluorine atom is relatively high, and the electrophilic reagent is more likely to attack this position. However, due to the electron-absorbing induction effect of the fluorine atom, the overall electron cloud density of the benzene ring will be reduced, making the reactivity slightly lower than that of benzene
Although the iodine atom has a large atomic radius, its p-orbital has a certain conjugation effect with the benzene ring π electron cloud, which also affects the distribution of the benzene ring electron cloud. At the same time, the iodine atom can be used as a leaving group, which can be replaced by nucleophilic reagents in some nucleophilic substitution reactions, and other organic compounds can be derived.
Cyanyl (CN) has strong electron-absorbing properties and can enhance the polarity of molecules. In this compound, cyanyl can participate in many chemical reactions, such as hydrolysis reactions. Under acidic or basic conditions, cyanyl can be hydrolyzed to carboxyl groups (-COOH); it can also participate in nucleophilic addition reactions. Cyanyl carbon atoms are partially positively charged and vulnerable to nucleophilic reagents.
In addition, the chemical properties of 2-fluoro-6-iodobenzonitrile are also affected by its intermolecular forces. Due to the presence of polar functional groups, there is a dipole-dipole force between molecules, which affects its melting point, boiling point and solubility. Generally speaking, its solubility in polar solvents is better than that in non-polar solvents.
What are the common synthetic methods of 2-fluoro-6-iodobenzonitrile?
The common synthesis methods of 2-fluoro-6-iodobenzonitrile, let me explain in detail.
First, 2-fluoro-6-aminobenzonitrile is used as the starting material. First, it is diazotized with sodium nitrite and hydroiodic acid. This process requires careful operation. In a low temperature environment, the sodium nitrite solution is slowly dropped into the mixture containing 2-fluoro-6-aminobenzonitrile and hydroiodic acid. Once the diazonium salt is formed, it immediately reacts with hydroiodic acid to obtain 2-fluoro-6-iodobenzonitrile. The steps of this method are relatively simple, but the diazotization reaction conditions are harsh, and precise temperature control and feeding rate are required to prevent side reactions from breeding.
Second, 2-fluorobenzonitrile is used as the starting material. First introduce iodine atoms through halogenation reaction. Usually, iodine elemental substance and suitable oxidants, such as hydrogen peroxide or potassium persulfate, can be selected. In an appropriate solvent, such as glacial acetic acid, heat and stir the reaction. The key to this reaction lies in the control of the amount of oxidant and the reaction temperature. Too much oxidant is easy to cause excessive halogenation; if the temperature is too high, the side reactions will be intensified. After halogenation, 2-fluoro-6-iodobenzonitrile can be obtained.
Third, 2-fluoro-6-halobenzene (the halogen atom is chlorine or bromine) is used as the raw material. First, Grignard's reagent is prepared, that is, 2-fluoro-6-halobenzene reacts with magnesium chips in anhydrous ether or tetrahydrofuran to form Grignard's reagent. Subsequently, Grignard's reagent reacts with iodine sources such as cuprous iodide, and the halogen atoms are replaced by iodine atoms to obtain 2-fluoro-6-iodobenzonitrile. This route requires an anhydrous and anaerobic environment, which requires high reaction equipment and operation.
All the above synthesis methods have their own advantages and disadvantages. In practical application, it is necessary to make a careful choice based on many factors such as the availability of raw materials, cost, reaction conditions, and the purity requirements of the target product.
2-fluoro-6-iodobenzonitrile in what areas
2-Fluoro-6-iodobenzonitrile has a wide range of uses. In the field of pharmaceutical synthesis, it is often used as a key intermediate. Due to the structure of benzonitrile and the characteristics of fluorine and iodine atoms, complex and biologically active compounds can be constructed through various chemical reactions. For example, when developing new antibacterial drugs, substances with high inhibitory activity against specific bacteria can be synthesized according to their structure modification; in the exploration of anti-tumor drugs, drug molecules that can be chemically modified to act precisely on tumor cell targets can be formed.
In the field of materials science, it also has important applications. With its unique chemical structure and electronic properties, it may be used to prepare functional organic materials. In the field of organic optoelectronic materials, materials with special optical and electrical properties can be synthesized through rational design for use in organic Light Emitting Diodes (OLEDs), organic solar cells and other devices to improve device performance and efficiency.
Furthermore, in the research and development of pesticides, 2-fluoro-6-iodobenzonitrile also has a place. It can be chemically converted to synthesize pesticide varieties that are highly effective in killing pests and are environmentally friendly. Due to its unique structure, pesticides with novel mechanisms of action may be developed to deal with pest resistance and improve crop yield and quality.
What is the market price of 2-fluoro-6-iodobenzonitrile?
2-Fluoro-6-iodobenzonitrile is a valuable organic synthesis intermediate in the field of fine chemicals. It is widely used in many fields such as medicinal chemistry and material science. However, its market price is difficult to generalize, because it is affected by many factors.
The first to bear the brunt is the market supply and demand situation. If the market demand for 2-fluoro-6-iodobenzonitrile is strong, but the supply is relatively scarce, just like the "rare is precious" principle, the price will rise; on the contrary, if the supply exceeds the demand, the price will tend to fall.
Furthermore, the production cost is also the key. The price of raw materials, the simplicity of the production process, and the amount of energy consumption are all closely related to the cost. The high price of raw materials, or the complex production process, requires a lot of manpower, material resources, and financial resources, and the cost will rise, which will in turn drive up the price of the product.
The scale of production also has an impact. In large-scale production, due to the scale effect, the unit production cost may be reduced, and the price may be more competitive; in small-scale production, the opposite is true.
The quality level should not be underestimated. High-purity 2-fluoro-6-iodobenzonitrile, due to the difficulty of preparation, can meet the needs of high-end applications, and the price is often higher than that of ordinary quality.
Regional differences also lead to different prices. Different regions have different levels of economic development, logistics costs, and market competition, and prices will vary. In economically developed regions, demand may be prosperous, but competition is also intense, and prices may be relatively stable; in places with inconvenient logistics, prices may be slightly higher due to increased transportation costs.
According to past market conditions and comprehensive considerations, the price of 2-fluoro-6-iodobenzonitrile fluctuates widely. For ordinary quality, the price per gram may be around tens of yuan to 100 yuan; for high purity and high quality, the price per gram may exceed 100 yuan, or even higher, reaching hundreds of yuan. But this is only a rough guess, and the actual price still needs to be investigated in detail according to the current market conditions. When purchasing, it is necessary to compare the quotations of different suppliers several times in order to obtain a better price.
What are 2-fluoro-6-iodobenzonitrile storage conditions?
2-Fluoro-6-iodobenzonitrile is an organic compound. When storing, specific conditions should be observed according to its characteristics to prevent deterioration, loss or potential safety hazards.
First environment selection. This compound should be stored in a cool place, because high temperature can easily promote its chemical reaction and cause its properties to change. It is better to choose a place with stable temperature, preferably 5 ° C - 25 ° C. In addition, it must be dry, because it is afraid of moisture, humid environment or hydrolysis and other reactions, which will damage its purity. Therefore, the humidity of the storage place should be controlled at 40% - 60%.
Second is the packaging requirement. Packaging materials must be compatible with 2-fluoro-6-iodobenzonitrile and do not chemically react with it. Commonly used glass containers or specific plastic containers. Glass containers have good chemical stability and can resist the interference of external substances; specific plastic containers are also optional if they can meet the inert requirements. Packaging must be tightly sealed to prevent the intrusion of air, water vapor, etc.
It is also necessary to pay attention to the ventilation of the storage location. Good ventilation can avoid the evaporation and accumulation of gases due to compounds and reduce safety risks. And should not be mixed with oxidants, acids, alkalis and other substances, because of their active chemical properties, contact with the above substances or cause violent reactions.
At the same time, the storage place should be clearly marked, indicating the compound name, characteristics, danger warning and other information, so that personnel can identify and deal with it. And the storage status should be regularly checked to see if the packaging is damaged, leaked, and the compound shows no signs of deterioration. If there is any abnormality, dispose of it in time to ensure its quality and safety.