2-Chloro-4-iodo-3-(trifluoromethyl)pyridine

2-Chloro-4-iodine-3- (trifluoromethyl) pyridine, this is an organic compound. Its physical properties are crucial, and it is related to many chemical processes and practical applications.
Looking at its properties, under room temperature and pressure, or in a solid state, it depends on the surrounding environmental conditions. The color of this compound is very likely to be white to light yellow crystalline powder, which can be used as an important basis for identification and analysis.
The melting point is also an important physical parameter. Accurate melting point determination helps to determine the purity and properties of the compound. It is hard to obtain the exact melting point data, but it can be speculated that due to the presence of halogen atoms and trifluoromethyl in the structure, the intermolecular force is enhanced, and the melting point may be relatively high.
The boiling point also cannot be ignored. The boiling point information is of great significance for operations such as distillation, separation and purification. Similarly, although there is no specific boiling point value, it can be inferred that due to the large polarity and mass of the molecule, its boiling point may be in a higher range.
In terms of solubility, in view of the lipophilic properties of chlorine, iodine atoms and trifluoromethyl in the structure, the compound may exhibit good solubility in organic solvents such as dichloromethane, chloroform, toluene, etc. However, in water, due to the large difference in polarity and water, the solubility may not be good.
In addition, the density of the compound is also a consideration. Although the exact density is unknown, it can be inferred from similar compounds that its density may be greater than that of water. Due to the presence of heavy atoms such as chlorine and iodine in the molecule, the mass per unit volume increases.
In summary, the physical properties of 2-chloro-4-iodine-3 - (trifluoromethyl) pyridine play an important guiding role in chemical research, chemical production and related fields. Although some data are missing, their properties can be roughly understood through structural analysis and analogy.

The chemical synthesis method of 2-chloro-4-iodine-3- (trifluoromethyl) pyridine has been known for a long time.
First, the compound containing the pyridine structure is used as the starting material. After halogenation, chlorine atoms and iodine atoms can be introduced. For this halogenation reaction, suitable halogenating reagents, such as reagents containing chlorine and iodine, need to be selected. Under specific reaction conditions, such as temperature and solvent selection, the halogenating reagent can fully interact with the pyridine compound, and the chlorine atom and iodine atom can be connected to the pyridine ring at the desired position. In addition, the introduction of trifluoromethyl can use the corresponding trifluoromethylation reagent, in a suitable reaction environment, so that the trifluoromethyl is connected to the pyridine ring, so that the target product can be obtained.
Second, other simple compounds are also used as the starting point, and the pyridine ring is constructed through a multi-step reaction. First, the carbon chain structure containing specific substituents is constructed through an organic reaction, and then the pyridine ring is formed through a cyclization reaction. During the cyclization process, the introduction positions and methods of chlorine atoms, iodine atoms and trifluoromethyl groups are also considered. This approach requires precise control of each step of the reaction, and the regulation of reaction conditions is particularly critical, such as the ratio of reactants, reaction temperature, reaction time, etc., will affect the yield and purity of the product.
Third, the reaction catalyzed by transition metals can also be used. Transition metal catalysts can effectively promote the transfer of halogen atoms and the formation of carbon-carbon and carbon-heteroatom bonds. With specific transition metal catalysts and suitable ligands, the precise integration of chlorine, iodine atoms and trifluoromethane on the pyridine ring can be achieved under mild reaction conditions. This method requires a high choice and dosage of catalysts, and requires careful preparation to achieve the desired reaction effect.
All these synthesis methods have their own advantages and disadvantages, and they need to be used according to the actual situation, such as the availability of raw materials, the difficulty of the reaction, and the purity requirements of the product.

2-Chloro-4-iodine-3- (trifluoromethyl) pyridine is useful in many fields. In the field of medicinal chemistry, this compound may be a key intermediate for the creation of new drugs. Due to its unique structure, it contains special groups such as chlorine, iodine and trifluoromethyl, which can interact with specific targets in organisms, or can help develop antibacterial, antiviral and even anticancer drugs. Special groups give it suitable physical and chemical properties, such as lipophilicity and electronic effects, which make it easier for drugs to penetrate biofilms and bind closely to targets for therapeutic purposes.
In the field of pesticide chemistry, it also has important value. It can be used as a raw material for the synthesis of highly efficient pesticides to resist the damage of pests and pathogens to crops. The combination of chlorine, iodine and trifluoromethyl may endow pesticides with excellent biological activity and stability, so that pesticides can play a more lasting role in the environment, effectively kill or inhibit pests and diseases, and have a relatively small impact on the environment, which is in line with the needs of modern green agriculture.
Furthermore, in the field of materials science, 2-chloro-4-iodine-3- (trifluoromethyl) pyridine may participate in the synthesis of functional materials. Due to its unique chemical structure, it may introduce special electrical, optical or thermal properties to materials. For example, in organic optoelectronic materials, the electron transport properties and light absorption properties of the material can be adjusted, providing the possibility for the preparation of high-performance Light Emitting Diodes, solar cells and other materials.
In the field of organic synthetic chemistry, this compound is often used as an important synthetic building block due to its polyfunctional properties. Chemists can modify and derive its structure through various organic reactions, such as nucleophilic substitution and coupling reactions, to construct more complex and diverse organic molecular structures, opening up new paths for the development of organic synthetic chemistry.

I think what you are asking is about the market price of 2-chloro-4-iodine-3 - (trifluoromethyl) pyridine. However, the market price of this compound often varies due to many factors, making it difficult to generalize.
First, the different manufacturers have a great impact on their prices. If the factory has advanced production technology, efficient operation mode, and can properly control costs, the 2-chloro-4-iodine-3 - (trifluoromethyl) pyridine produced may be more expensive. On the contrary, if the manufacturer's production technology is backward and the operating cost is high, the price of its products may be higher.
Second, the market supply and demand relationship is also a key factor. If the market demand for 2-chloro-4-iodine-3- (trifluoromethyl) pyridine is strong and the supply is relatively short, the price will rise. On the contrary, if the market demand is weak and the supply is excessive, the price may fall.
Third, fluctuations in the price of raw materials will also affect the price of this compound. If the price of raw materials required to produce 2-chloro-4-iodine-3 - (trifluoromethyl) pyridine fluctuates sharply, the cost of the product will also change accordingly, which will affect the market price.
Fourth, the difference in Quality Standards is also related to price. If the product is of high quality and meets the requirements of high purity and impurity content, its price may be higher than that of ordinary quality products.
Combining the above factors, if you want to know the exact market price of 2-chloro-4-iodine-3- (trifluoromethyl) pyridine, you should consult a professional chemical product supplier or dealer, or refer to the quotation information of the relevant chemical product trading platform, so as to obtain more accurate price details.

2-Chloro-4-iodine-3- (trifluoromethyl) pyridine is an organic chemical substance. Its storage conditions are crucial and related to the stability and quality of this substance.
This substance is quite sensitive to air and moisture. Therefore, it should be stored in a cool, dry and well-ventilated place. If it is in a high temperature place, or due to heat, its chemical properties will change, which will damage its quality. And moisture can easily lead to reactions such as hydrolysis, causing it to deteriorate.
And it must be kept away from fires and heat sources to prevent fires. Because it is an organic compound, it is mostly flammable, and it is dangerous to encounter open fires and hot topics. In the storage place, suitable fire equipment should be prepared to prevent accidents.
In addition, it needs to be stored separately from oxidizing agents, acids, alkalis, etc., and must not be mixed. Due to its active chemical properties, it may encounter various chemicals or cause violent chemical reactions, which may pose a safety risk.
In the choice of storage containers, it should not be ignored. A sealed container should be used to prevent air and moisture from invading. And the material of the container should not react with 2-chloro-4-iodine-3- (trifluoromethyl) pyridine to ensure the purity of this substance.
When storing daily, it should be checked regularly. Observe whether its appearance and properties have changed, measure its relevant indicators, and if there is any abnormality, dispose of it properly. In this way, to ensure the stability of 2-chloro-4-iodine-3 - (trifluoromethyl) pyridine during storage.