2 Chloro 3 Iodopyridine
Iodobenzene

2 Chloro 3 Iodopyridine

Fengxi Chemical

Specifications

HS Code

287948

Chemical Formula C5H3ClIN
Molecular Weight 239.44
Appearance Solid (Typical for many organic halopyridines)
Boiling Point Estimated based on similar compounds, around 240 - 260°C (approximate, can vary depending on purity and pressure)
Melting Point Data might be limited, estimated based on related compounds, around 30 - 50°C (approximate)
Solubility In Water Poorly soluble, like most halogenated heterocyclic compounds
Solubility In Organic Solvents Soluble in common organic solvents such as dichloromethane, chloroform, and ethyl acetate
Flash Point Estimated to be around 100 - 120°C (approximate, based on similar halogenated pyridines)
Stability Stable under normal conditions, but can react with strong oxidizing agents and reducing agents
Chemical Formula C5H3ClIN
Molar Mass 255.44 g/mol
Appearance Solid (presumably, based on similar compounds)
Solubility In Water Low (due to non - polar aromatic structure and presence of halogens)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Reactivity Reactive towards nucleophiles due to the presence of chlorine and iodine which can be displaced
Chemical Formula C5H3ClIN
Molecular Weight 241.44
Appearance Solid (usually)
Odor Typical organic compound odor
Melting Point Data specific to the compound needed
Boiling Point Data specific to the compound needed
Density Data specific to the compound needed
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Flash Point Data specific to the compound needed
Stability Stable under normal conditions but reactive with strong oxidizing agents
Name 2-chloro-3-iodopyridine
Molecular Formula C5H3ClIN
Molecular Weight 239.44
Appearance Solid (likely, typical for many such organic compounds)
Boiling Point Data needed
Melting Point Data needed
Density Data needed
Solubility In Water Low solubility expected, due to non - polar nature of the organic ring
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Flash Point Data needed
Vapor Pressure Data needed
Pka Data needed
Packing & Storage
Packing 2 - chloro - 3 - iodopyridine packaged in 100 - gram bottles for secure storage and transport.
Storage 2 - Chloro - 3 - iodopyridine should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly - sealed container to prevent moisture absorption and potential degradation. It should be separated from incompatible substances. Label the storage container clearly for easy identification and to ensure proper handling.
Shipping 2 - chloro - 3 - iodopyridine is shipped in sealed, corrosion - resistant containers. Compliance with hazardous chemical shipping regulations is ensured. Adequate labeling indicates its nature, and it's transported with precautions to prevent breakage and leakage.
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2-chloro-3-iodopyridine 2-chloro-3-iodopyridine 2-chloro-3-iodopyridine
General Information
Frequently Asked Questions
What are the physical properties of 2-chloro-3-iodopyridine?
2-Chloro-3-iodopyridine, which is an organic compound. Looking at its physical properties, at room temperature, this substance is mostly in a solid state, but its specific melting point has not yet been determined, and it needs to be accurately determined by professional experiments. Its appearance may be a white to light yellow crystalline powder. Due to the introduction of halogen atoms, the intermolecular force changes.
On solubility, because it contains polar pyridine rings and halogen atoms, it should have a certain solubility in polar organic solvents, such as methanol, ethanol, dichloromethane, etc. Halogen atoms are lipophilic, so that they can be better dispersed in some organic solvents. However, in water, due to the limited force between water molecules and organic molecules, the solubility may be low.
Furthermore, its volatility is relatively large due to the relatively large molecule, and the mass of the halogen atom is large, the van der Waals force is strong, and the volatility is weak. Under normal circumstances, it is not easy to volatilize into the air.
Its density is greater than that of general pyridine compounds due to the substitution of halogen atoms. The relative atomic weight of halogen atoms is large, which increases the molecular weight and increases the density.
In addition, the stability of this substance is due to the conjugation of halogen atoms with pyridine rings, which has certain stability. However, it encounters special chemical reagents such as strong reducing agents, strong acids, and strong bases, or chemical reactions may occur to cause structural changes. In conclusion, the physical properties of 2-chloro-3-iodine pyridine are influenced by the pyridine ring and the halogen atom, and their applications in organic synthesis are closely related to these properties.
What are the chemical properties of 2-chloro-3-iodopyridine?
2-Chloro-3-iodine pyridine, this is an organic compound. Its molecules contain chlorine atoms and iodine atoms, which are connected to specific positions in the pyridine ring. Due to the electronegativity of chlorine and iodine atoms and the conjugation system of the pyridine ring, the substance has unique chemical properties.
In terms of nucleophilic substitution reaction, the chlorine and iodine atoms of this compound can form a check point for the attack of nucleophilic reagents. Chlorine atoms are relatively active, and nucleophilic reagents such as alkoxides and amines can react with them to replace chlorine atoms and form new organic compounds. For example, the attack of alkoxides can generate corresponding ether derivatives; the reaction of amines can obtain nitrogen-containing substitution products. Although the iodine atom is slightly more stable than the chlorine atom, under certain conditions, it can also participate in nucleophilic substitution, because the negative ions formed after the iodine atom leaves are relatively stable.
Let's talk about its redox properties. The nitrogen atom of the pyridine ring has lone pair electrons and can participate in the redox process. Under the action of appropriate oxidants, the pyridine ring may be oxidized, changing its electron cloud distribution and affecting the reactivity of chlorine and iodine atoms. At the same time, in some reduction systems of this compound, chlorine and iodine atoms may be reduced and removed to form pyridine derivatives.
And because its structure contains halogen atoms, 2-chloro-3-iodine pyridine can also play a role in the coupling reaction catalyzed by metals. For example, under palladium catalysis, it can be coupled with compounds containing borate esters to form carbon-carbon bonds and synthesize more complex organic molecules, which is of great significance in the field of organic synthetic chemistry, assisting chemists in creating organic materials with diverse structures, pharmaceutical intermediates, etc.
In short, the rich chemical properties of 2-chloro-3-iodopyridine provide many possibilities for organic synthetic chemistry, and many valuable compounds can be derived through different reaction conditions and reagents.
What are 2-chloro-3-iodopyridine synthesis methods?
2-Chloro-3-iodopyridine is also an organic compound. There are several common methods for its synthesis.
One is to take pyridine as the starting material and obtain it by halogenation. First, pyridine can be reacted with chlorine sources such as chlorine gas and chlorinating agents under the conditions of constant temperature and pressure and the presence of catalysts, and chlorine atoms can be introduced into the 2-position of the pyridine ring to obtain 2-chloropyridine. Then let 2-chloropyridine and iodine source, such as iodine elemental substance and appropriate oxidant, act in a suitable reaction environment, so that iodine atoms are introduced into the third position, and finally 2-chloro-3-iodine is obtained. In this way, the control of chlorination and iodine reaction conditions is quite important, such as temperature, amount of catalyst, ratio of reactants, etc., all of which are related to the yield and purity of the product.
Second, or can be started from pyridine derivatives with specific substituents. If there are compounds with partially convertible groups on the pyridine ring, they are obtained through a series of functional group conversion reactions. For example, the group on a pyridine derivative can be gradually converted into chlorine atoms and iodine atoms by suitable reagents and reactions, and its substitution at the 2nd and 3rd positions can be precisely controlled. This approach requires detailed design of the structure of the starting derivative, and familiarity with the mechanism and conditions of the conversion of each functional group, in order to achieve the purpose of synthesis smoothly.
Third, there are also those based on the coupling reaction catalyzed by transition metals. Select suitable halogenated pyridine derivatives, and react with chlorine sources and iodine catalysts derived from transition metals, such as palladium, nickel, etc., to obtain 2-chloro-3-iodopyridine through coupling reaction. Among them, the activity of transition metal catalysts, the choice of ligands, the type of reaction solvent and base all have a great influence on the process and result of the reaction. Only by adjusting various factors can the reaction efficiency be improved and the target product be obtained.
What are the main uses of 2-chloro-3-iodopyridine?
2-Chloro-3-iodopyridine is also an organic compound. It has a wide range of uses and plays an important role in the field of organic synthesis.
First, it is often a key intermediate in drug synthesis. Due to the unique structure of the pyridine ring, the compound is endowed with special chemical activity and pharmacological properties. In the process of many drug development, 2-chloro-3-iodopyridine is used as the starting material, and through a series of chemical reactions, molecular structures with specific pharmacological activities can be constructed. For example, in the synthesis of some antibacterial drugs, by modifying and transforming their functional groups, drug molecules with high inhibitory effect on specific bacteria can be obtained.
Second, it is also used in the field of materials science. Materials with special optoelectronic properties can be prepared by polymerization or combination with other functional materials. For example, in the preparation of organic optoelectronic materials, the introduction of 2-chloro-3-iodopyridine structure can adjust the electronic transport properties and optical absorption properties of the materials, providing possibilities for the development of new optoelectronic devices, such as organic Light Emitting Diode (OLED), solar cells, etc.
Third, it plays an important role in the synthesis of pesticides. Pesticides with high insecticidal, bactericidal or herbicidal activities can be synthesized through chemical modification. The presence of its pyridine ring and halogen atoms helps to enhance the interaction between pesticides and specific receptors or enzymes in target organisms, improve the biological activity and selectivity of pesticides, and reduce the impact on non-target organisms.
In short, 2-chloro-3-iodopyridine has shown important application value in many fields such as drugs, materials and pesticides due to its unique chemical structure, providing a key material basis and technical support for the development of related industries.
What are the precautions in storage and transportation of 2-chloro-3-iodopyridine?
2-Chloro-3-iodopyridine is an organic compound. During storage and transportation, many matters need to be paid special attention.
First, when storing, be sure to choose a cool, dry and well-ventilated place. This compound may decompose or deteriorate when heated or damp. The temperature of the warehouse should be maintained in an appropriate range, and the humidity should also be strictly controlled to prevent damage to its moisture absorption.
Second, because of its certain chemical activity, it needs to be stored separately from oxidants, strong bases, strong acids and other substances. Contact with these substances is very likely to trigger violent chemical reactions, or even cause serious consequences such as explosions. Just like water and fire are incompatible, contact between the two will inevitably change.
Third, the storage container needs to be carefully selected. Corrosion-resistant materials should be used, such as glass bottles or specific plastic containers, and ensure a tight seal. In this way, it can not only prevent its volatilization and leakage, but also avoid reactions with external substances.
Fourth, during transportation, strict transportation specifications should be followed. The packaging must be stable to prevent the container from breaking during handling and bumping. At the same time, the transportation vehicle needs to be equipped with corresponding emergency treatment equipment to prepare for emergencies. In case of leakage, effective emergency measures need to be taken quickly to prevent the spread of pollution.
Fifth, whether it is storage or transportation, the relevant operators should be professionally trained and familiar with the characteristics of the compound and emergency treatment methods. In the event of an emergency, be able to respond calmly and minimize the harm.
In short, the storage and transportation of 2-chloro-3-iodopyridine needs to be strictly controlled in terms of environment, material isolation, container selection, transportation specifications, and personnel training, and must not be slack in order to ensure safety.