2 Chloro 5 Iodo 6 Methylpyridine
Iodobenzene

2 Chloro 5 Iodo 6 Methylpyridine

Fengxi Chemical

Specifications

HS Code

666830

Chemical Formula C6H5ClIN
Molar Mass 271.468 g/mol
Appearance Solid (likely, based on similar compounds)
Physical State At Room Temperature Solid
Solubility In Water Low (organic compound with non - polar groups)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Chemical Formula C6H5ClIN
Molecular Weight 271.47
Appearance Solid (predicted)
Solubility In Water Insoluble (predicted)
Solubility In Organic Solvents Soluble in common organic solvents (predicted)
Chemical Formula C6H5ClIN
Molecular Weight 270.47
Appearance Solid (predicted)
Boiling Point Estimated around 260 - 280 °C
Density Estimated value considering similar halogen - containing pyridines
Solubility In Water Low solubility in water due to non - polar nature of the molecule
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, etc.
Vapor Pressure Low vapor pressure at room temperature
Stability Stable under normal conditions but may react with strong oxidizing agents
Chemical Formula C6H5ClIN
Molar Mass 271.469 g/mol
Appearance Solid (likely, based on similar compounds)
Physical State At Room Temp Solid
Solubility In Water Low (non - polar nature due to organic structure and halogen atoms)
Solubility In Organic Solvents Soluble in non - polar and some polar organic solvents like dichloromethane, chloroform
Odor Typically has a characteristic organic odor, likely pungent due to halogens
Packing & Storage
Packing 100g of 2 - chloro - 5 - iodo - 6 - methylpyridine packaged in a sealed glass bottle.
Storage Store 2 - chloro - 5 - iodo - 6 - methylpyridine in a cool, dry, well - ventilated area away from heat sources and open flames. Keep it in a tightly sealed container to prevent exposure to air and moisture, which could potentially cause decomposition. Store separately from oxidizing agents and incompatible substances to avoid chemical reactions.
Shipping 2 - chloro - 5 - iodo - 6 - methylpyridine, a chemical, is shipped in sealed, corrosion - resistant containers. It follows strict hazardous material regulations, with proper labeling and secure packaging to prevent leakage during transit.
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2 Chloro 5 Iodo 6 Methylpyridine 2 Chloro 5 Iodo 6 Methylpyridine 2 Chloro 5 Iodo 6 Methylpyridine
General Information
Frequently Asked Questions
What are the physical properties of 2-chloro-5-iodo-6-methylpyridine?
2-Chloro-5-iodine-6-methylpyridine, this is a kind of organic compound. Its physical properties are related to the external characterization and basic characteristics of the substance, and are quite important.
First appearance, under normal conditions, it may be a colorless to light yellow liquid, or a crystalline solid. The judgment of this morphology is due to different preparation conditions and environmental factors. If the preparation conditions such as temperature and pressure are different, the condensed state will be different.
The melting point has been investigated by many experiments, and it is generally within a certain range. However, the exact value often fluctuates slightly due to differences in the amount of impurities and test methods. Generally speaking, its melting point or in a specific range, at this temperature, the substance changes from solid to liquid. This property is of great significance in the process of separation, purification and identification of compounds. The purity geometry of the compound can be determined by means of melting point determination.
In addition, the boiling point also has a corresponding value under a specific pressure environment. The level of its boiling point is closely related to the intermolecular forces. Interactions such as van der Waals forces and hydrogen bonds exist between 2-chloro-5-iodine-6-methylpyridine molecules, and the strength of these interactions determines the boiling point. Knowing the boiling point is crucial in separation operations such as distillation, and can help determine the appropriate temperature to achieve effective separation.
In terms of solubility, it may have some solubility in common organic solvents, such as ethanol, ether, dichloromethane, etc. In water, due to the structure of the compound containing hydrophobic groups, its solubility in water is not good. This solubility characteristic plays a significant role in the solvent selection and product separation of organic synthesis reactions. According to its solubility, a suitable solvent can be selected to promote the smooth progress of the reaction and the efficient separation of the product.
Density is also one of the important physical properties. Its density may be similar to that of common organic solvents, and the specific value is greatly affected by temperature. When the temperature increases, the thermal movement of molecules intensifies, the molecular spacing increases, and the density decreases accordingly; conversely, when the temperature decreases, the density increases.
In addition, the compound may have a certain odor, but the degree of odor is different due to the amount of content and individual olfactory sensitivity. Its odor may be a special organic odor. During actual operation and use, attention should be paid to ventilation to prevent discomfort to the human body.
In summary, the physical properties of 2-chloro-5-iodine-6-methylpyridine, such as appearance, melting point, boiling point, solubility, density and odor, play an indispensable role in organic synthesis, analysis and identification, and practical application. In-depth understanding of these properties can better control the compound and make it play its due role in various fields.
What are the chemical properties of 2-chloro-5-iodo-6-methylpyridine?
2-Chloro-5-iodine-6-methylpyridine is one of the organic compounds. It has the structure of halogenated pyridine, and chlorine, iodine and methyl are respectively connected to specific positions in the pyridine ring. The chemical properties of this substance are unique and worthy of investigation.
First, due to the existence of halogen atoms and methyl groups, the electron cloud distribution is different from that of the pyridine body. Chlorine and iodine have high electronegativity and have electron-absorbing induction effects, which can reduce the electron cloud density of the pyridine ring and change the electrophilic substitution reaction activity on the ring. Compared with pyridine, the check point and rate of electrophilic substitution of this compound may be different. The superconjugation effect of methyl to electrons or partially cancels the electron-withdrawing effect of halogen atoms, which affects the reaction selectivity.
Secondly, halogen atoms can participate in a variety of reactions. Chlorine and iodine atoms are active and can undergo nucleophilic substitution reactions. Under suitable nucleophilic reagents and reaction conditions, chlorine or iodine can be replaced to form new derivatives, such as reacting with sodium alcohol or ether products; reacting with amines or forming nitrogen-containing derivatives, which is an important way to synthesize complex organic compounds.
Furthermore, due to the conjugated structure of the pyridine ring, 2-chloro-5-iodine-6-methylpyridine may have certain stability and aromaticity, and can participate in some reactions based on aromatic rings, such as oxidation and reduction reactions. The presence of the pyridine ring makes the molecule alkaline to a certain extent, and forms salts under acidic conditions or protonation.
In short, 2-chloro-5-iodine-6-methylpyridine has important uses in organic synthesis, medicinal chemistry and other fields due to its special structure. Its unique chemical properties lay the foundation for related research and applications.
What are 2-chloro-5-iodo-6-methylpyridine synthesis methods?
The synthesis method of 2-chloro-5-iodine-6-methylpyridine is a very important research content in the field of organic synthesis. The common synthesis path is to use the compound containing the pyridine structure as the starting material, and to introduce the chlorine atom and the iodine atom through the halogenation reaction, and to realize the introduction of the methyl group at the same time.
First, 6-methylpyridine can be selected as the starting material. First, a suitable chlorination reagent, such as thionyl chloride or phosphorus oxychloride, is used under suitable reaction conditions to chlorinate the specific position on the pyridine ring to generate 2-chloro-6-methylpyridine. In this step, factors such as reaction temperature, reaction time, and reagent dosage all have a significant impact on the yield and selectivity of the reaction. Usually, the reaction temperature needs to be strictly controlled, or the reaction should be started at a low temperature, and then gradually heated to a moderate temperature to ensure that the chlorination reaction mainly occurs at the second position.
After 2-chloro-6-methylpyridine is obtained, the iodization reaction is carried out. Commonly used iodizing reagents such as mixtures of iodine elemental substance and potassium iodide, in the presence of oxidants such as hydrogen peroxide or nitric acid, induce the introduction of iodine atoms into the fifth position. The type and amount of oxidant, as well as the pH of the reaction system, are all key factors affecting the iodization reaction. For example, selecting a mild oxidizing agent and precisely adjusting its dosage can reduce the occurrence of side reactions and increase the yield of 2-chloro-5-iodine-6-methylpyridine.
Second, other pyridine derivatives can also be used as starting materials. If some substituents already exist on the pyridine ring of the starting material, the target substituents can be gradually introduced through selective substituent conversion reactions. For example, if there are groups that can be converted into methyl groups on the starting pyridine ring, a methylation reaction can be carried out first; then, chlorine atoms and iodine atoms are introduced in sequence according to the reactivity and positioning laws. This process requires a deep understanding of the mechanism and conditions of each step of the reaction in order to precisely control the reaction process and obtain high-purity 2-chloro-5-iodine-6-methylpyridine.
In addition, during the reaction process, analytical methods such as thin-layer chromatography (TLC), gas chromatography (GC) or high-performance liquid chromatography (HPLC) are used to monitor the reaction process in real time to ensure that the reaction proceeds in the expected direction. Product separation and purification are also very important, and column chromatography and recrystallization are often used to obtain high-purity 2-chloro-5-iodine-6-methylpyridine to meet the needs of subsequent experiments or industrial applications.
What are the main uses of 2-chloro-5-iodo-6-methylpyridine?
2-Chloro-5-iodine-6-methylpyridine is also an organic compound. It has a wide range of uses and is often a key intermediate in the field of pharmaceutical synthesis. To cover the creation of medicine, an exquisite molecular structure is required. The unique structure of this compound can pave the way for the development of new drugs. Chemists can use its activity check point to derive a variety of derivatives to explore molecules with specific pharmacological activities, which is expected to become a good medicine for curing diseases and saving people.
In the field of pesticide synthesis, it also plays an important role. The effect of pesticides is related to the prosperity of crops. 2-Chloro-5-iodine-6-methylpyridine can be used as a starting material, and through a series of reactions, high-efficiency pesticides can be prepared. Such pesticides can precisely combat pests and diseases, and are environmentally friendly, reduce pollution, and maintain the sustainable development of agriculture.
Furthermore, in the field of materials science, there are also opportunities for application. With the advance of science and technology, the demand for special materials is increasing. This compound may participate in the preparation of materials with unique properties, such as optoelectronic materials. Its structural properties may endow materials with special optical and electrical properties, which play an important role in electronic devices, optical equipment, etc., and promote the development of related fields. In conclusion, although 2-chloro-5-iodine-6-methylpyridine is a micro molecule, it has great potential in many fields, providing opportunities for the progress of many industries.
2-chloro-5-iodo-6-methylpyridine what are the precautions in storage and transportation?
2-Chloro-5-iodine-6-methylpyridine is an organic chemical. When storing and transporting, many things should be paid attention to to to avoid safety risks or quality deterioration.
First, storage temperature and environment are critical. This chemical should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Because it is quite sensitive to temperature, high temperature can easily promote its decomposition or initiate chemical reactions. If the temperature is too high, the chemical bonds in the molecule may become active, causing structural changes and affecting its chemical properties. And humid environment or causing reactions such as hydrolysis, so be sure to keep the storage place dry.
Second, avoid contact with incompatible substances. 2-Chloro-5-iodine-6-methylpyridine may react violently with strong oxidants, strong bases, etc. Oxidants will oxidize it, change the molecular structure; strong bases may cause substitution, elimination and other reactions. Therefore, when storing, it should be separated from such substances and clearly marked to prevent mismixing.
Third, the transportation packaging should be stable and sealed. Vibration and collision during transportation are unavoidable. If the packaging is not firm, it is easy to cause damage to the container and leakage of chemicals. Good sealing can prevent it from volatilizing and avoid contact with outside air and moisture. Containers of commonly used glass, plastic and other materials should be ensured to be free of damage and leakage before use.
Fourth, follow regulations and standards. Storage and transportation of this chemical must be strictly in accordance with relevant national and local regulations. From packaging labels to shipping documents, compliance is required. Packaging labels should clearly indicate the name, nature, hazards and other information of the chemical, and transportation documents should be complete, recording the transportation route, time, person in charge, etc., for traceability.
Fifth, personnel protection is indispensable. Personnel exposed to this chemical should wear appropriate protective equipment, such as protective clothing, gloves, goggles, etc. Because of its irritation and toxicity, direct contact or skin, eye damage, inhalation or absorption through the skin will also threaten health. Therefore, personnel protection is the guarantee of storage and transportation safety.