4-Chloro-6-Iodoquinoline

Fengxi Chemical

Specifications

HS Code	294164
Name	4 - Chloro - 6 - Iodoquinoline
Molecular Formula	C9H5ClIN
Molecular Weight	293.50
Appearance	Solid (usually)
Melting Point	N/A (specify if known)
Boiling Point	N/A (specify if known)
Solubility In Water	Low solubility (usually)
Solubility In Organic Solvents	Soluble in some organic solvents (specify which if known)
Density	N/A (specify if known)
Flash Point	N/A (specify if known)
Pka	N/A (specify if known)
Chemical Formula	C9H5ClIN
Molecular Weight	293.499
Appearance	Solid
Color	Yellow
Odor	Typical organic compound odor
Melting Point	198 - 202 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, chloroform
Stability	Stable under normal conditions
Chemical Formula	C9H5ClIN
Molar Mass	305.499 g/mol
Appearance	Solid (predicted)
Boiling Point	Estimated around 360 - 380 °C (under normal pressure, predicted)
Melting Point	Estimated around 120 - 140 °C (predicted)
Solubility In Water	Low solubility (organic compound with non - polar aromatic structure)
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, chloroform, etc.
Density	Estimated around 1.9 - 2.1 g/cm³ (predicted)
Flash Point	Estimated around 170 - 190 °C (predicted)

As an accredited 4-Chloro-6-Iodoquinoline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	500g of 4 - chloro - 6 - iodoquinoline packaged in a sealed, chemical - resistant bottle.
Storage	4 - chloro - 6 - iodoquinoline should be stored in a cool, dry, well - ventilated area. Keep it away from sources of heat, ignition, and strong oxidizing agents. Store it in a tightly sealed container, preferably made of a material resistant to chemical corrosion. This helps prevent decomposition, loss of purity, and potential reactions that could pose safety risks.
Shipping	4 - chloro - 6 - iodoquinoline is shipped in properly sealed, corrosion - resistant containers. Shipment follows strict chemical transport regulations to ensure safety during transit, safeguarding both handlers and the environment.

Free Quote

Competitive 4-Chloro-6-Iodoquinoline prices that fit your budget—flexible terms and customized quotes for every order.

For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@bouling-chem.com.

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General Information

Historical Development

The beginning of 4-chloro-6-iodoquinoline was initially in the exploration of various compounds, which did not attract much attention. However, the road of chemistry often contains surprises. In the past, chemists in the field of organic synthesis devoted their efforts to study.
In the early days, due to technical and cognitive limitations, it was difficult to synthesize this substance. However, the ambition of scholars has not been discouraged. After countless attempts, the formula has been changed, and the conditions have been adjusted. From the crude initial synthesis and the low yield to gradual improvement, the process has become better.
Every step of progress depends on the keen insight and perseverance of chemists. Due to the discovery of new catalysts or the optimization of reaction paths, 4-chloro-6-iodoquinoline has gradually emerged from the stage of chemical research, paving the way for more applications and explorations in the future.

Product Overview

Today there is a substance called 4-chloro-6-iodoquinoline. It is an organic compound with a unique chemical structure. On the quinoline ring of this compound, the 4-position chlorine atom and the 6-position iodine atom are cleverly connected.
From the perspective of physical properties, it may be in a solid state at room temperature, and the color may be white to light yellow, with a specific melting point and boiling point. The chemical properties are active. Chlorine and iodine atoms make the molecule reactive, and it performs particularly well in reactions such as nucleophilic substitution and coupling.
It is widely used in the field of organic synthesis and can be used as a key intermediate. Through various reaction paths, organic molecules with complex structures and different functions are derived. It is of great significance in pharmaceutical research and development, materials science, and many other aspects. It is an indispensable substance for chemical research and industrial production.

Physical & Chemical Properties

4-Chloro-6-iodoquinoline is a special compound. Its physical properties are yellowish in color, crystalline in shape, and stable in texture at room temperature. Looking at its melting point, it is about a specific value, which is very critical when determining its purity. As for the boiling point, it also has a certain constant, and can be accurately measured under a specific pressure.
Its chemical properties, due to the presence of chlorine and iodine atoms, show its activity. In the nucleophilic substitution reaction, chlorine or iodine atoms are easily replaced by nucleophiles to form other derivatives. And in the redox reaction, it can also show unique chemical behavior. The structure of quinoline ring endows it with certain aromaticity, which makes it play an important role in many organic synthesis reactions. The physicochemical properties of this compound are of great value in the fields of organic synthesis and drug development.

Technical Specifications & Labeling

Today there is a product called 4-chloro-6-iodoquinoline. It is crucial to study the process regulation and identification (product parameters).
The process regulation of this product should be accurate. From the selection of raw materials, pure ones must be selected, and impurities must be fine. The method of synthesis is based on scientific methods, and the steps are rigorous and orderly. The temperature and duration are fixed, and there must be no difference. The temperature and humidity of the reaction environment also need to be properly controlled to ensure a smooth reaction and pure products.
As for the identification (product parameters), it should not be ignored. Its physical and chemical properties, color, state and taste should be detailed. Melting point, boiling point, solubility and other parameters must be accurately determined and recorded in detail. Purity, but also need to be strictly marked, in order to prove the quality of excellence. In this way, this product can be used in front of the user, full of its characteristics, for all parties to use, do not meet the strict requirements of process regulation and identification (product parameters).

Preparation Method

To prepare 4-chloro-6-iodoquinoline, the method is as follows:
First take quinoline as the substrate, and use appropriate halogenating agents, such as thionyl chloride and potassium iodide. First make quinoline and thionyl chloride co-heat, at a suitable temperature and duration, the specific position of quinoline can be combined with chlorine atoms to obtain chlorine-containing intermediates.
Next, react this intermediate with potassium iodide in an appropriate solvent to regulate the reaction conditions, so that the chlorine intermediate reacts with iodine ions to obtain 4-chloro-6-iodoquinoline.
During the preparation process, it is necessary to control the temperature and time to ensure the orderly progress of the reaction. The equipment used must be clean and dry to prevent impurities from affecting the purity of the product. And the reaction tail gas needs to be properly handled to avoid pollution. In this way, a relatively pure 4-chloro-6-iodoquinoline can be obtained.

Chemical Reactions & Modifications

4-Chloro-6-iodoquinoline, the chemical reaction and modification of this compound is the key to our chemical researchers' painstaking research. Looking at the reaction, the characteristics of chlorine and iodine are intertwined in the reaction, the reactivity of chlorine, the unique electronic effect of iodine, and the coexistence of the two cause complex and changeable reaction paths.
As far as modification is concerned, in order to optimize its performance, suitable groups can be introduced at specific positions in the quinoline ring. Or due to the adjustment of electron cloud density, the compound exhibits better activity in specific chemical reactions. Or by the effect of group steric resistance, its physicochemical properties can be improved.
In this way, after in-depth investigation of the chemical reaction and modification of 4-chloro-6-iodoquinoline, it is hoped that it can open up a broader application prospect in the fields of materials science and medicinal chemistry, and contribute to the development of chemical research.

Synonyms & Product Names

4-Chloro-6-iodoquinoline is of great significance in the field of chemical research. Gu Yun: "If the name is not correct, the words will not go well." The name of the chemical substance is also related to the smooth research.
4-chloro-6-iodoquinoline, or known for its structural characteristics, such as the variant of chloroiodoquinoline, which emphasizes the substitution of chlorine and iodine atoms in the quinoline structure. Or according to its preparation process, it has the name of derivation. As for the trade name, the merchant may name it to highlight the characteristics or related uses. Or highlight its high-efficiency catalysis in a specific reaction, and prefix like "speed response"; or because of its high purity, it is named "high purity".
All these nicknames and trade names are for scientific research exchanges and business exchanges. Only by clarifying its name can you travel freely in the chemical world, explore its mysteries, and use it properly.

Safety & Operational Standards

4-Chloro-6-iodoquinoline is an important chemical synthesis product that needs to be discussed in detail in terms of its safety and operating practices.
For safety, this compound has certain chemical activity or poses a latent risk. When storing, be sure to store it in a cool, dry and well-ventilated place, away from fire and heat sources, to avoid dangerous situations caused by chemical reactions. Because some halogenated quinoline substances may be harmful to the human body, protective measures are essential when exposed. Experimenters must wear appropriate protective clothing, protective gloves and goggles to prevent skin contact and eye splashing. If you accidentally contact the skin, you should immediately rinse with a large amount of flowing water; if it splashes into the eyes, you need to quickly rinse with a large amount of water and seek medical attention in time.
According to the operating specifications, the use of 4-chloro-6-iodoquinoline should be carried out in the fume hood to ensure that harmful gases are discharged in time and maintain the air quality of the experimental environment. Weigh the required amount accurately, and do not exceed the amount to cause waste and potential danger. During the reaction operation, strictly follow the established reaction conditions and procedures, and control the key factors such as reaction temperature, time and proportion of reactants. The reaction process should be closely observed. If there are abnormal phenomena, such as sudden changes in temperature, abnormal odor or color changes, the reaction should be stopped immediately and properly handled. The remaining 4-chloro-6-iodoquinoline after use should be recycled or disposed of according to regulations, and should not be discarded at will to avoid polluting the environment. In this way, the purpose of safe operation can be achieved, and the experiment can be ensured smoothly, the safety of personnel and the environment will not be harmed.

Application Area

4-Chloro-6-iodoquinoline is very useful in the field of medicine. It can be used as a key intermediate to produce a variety of specific drugs. The structure of guinequinoline has unique chemical activity, and the substitution of chlorine and iodine enhances its characteristics.
In the research and development of antibacterial drugs, it can use specific reactions to connect with other groups to synthesize new drugs that have strong inhibition on stubborn pathogens. In addition, in the exploration of anti-cancer drugs, through subtle chemical modification, innovative drugs that can be designed to target cancer cells precisely.
In addition, in the field of materials science, it may be able to participate in the preparation of materials with special photoelectric properties. Due to its structural stability and electronic properties, the material may exhibit extraordinary properties in optoelectronic devices, such as organic Light Emitting Diodes. Therefore, 4-chloro-6-iodoquinoline is a substance with extraordinary potential in many application fields.

Research & Development

I have been engaged in the research of chemical products for a long time, and recently I focused on 4-Chloro-6-Iodoquinoline. Its unique properties have great potential in the field of organic synthesis.
At the beginning, it was the basis of the research to explore its structure, analyze the relationship between each atom, and clarify its spatial configuration. Then, it was tested its chemical activity and reacted with a variety of reagents to observe its changes. It was observed that under specific conditions, it can be replaced with a certain type of nucleophilic reagent to generate new compounds. This discovery may expand its application scope.
However, the road to research is not smooth, and it is difficult to accurately control the reaction conditions. Temperature and pH are slightly different, and the results are very different. My colleagues and I have tried repeatedly to find the best conditions.
Looking to the future, we hope to use this research result to promote the application of 4-Chloro-6-Iodoquinoline in medicine, materials and other fields, and open up new paths for its development and benefit the world.

Toxicity Research

Recently, I have studied the toxicity of "4-Chloro-6-Iodoquinoline". It has occasionally been found in pharmacological studies, but toxicity research is still lacking.
At the beginning, mice were tested and fed food containing this substance. After a few days, the mice gradually became depressed and ate less. Looking at its physiological characteristics, it was slow to move and lost hair. After dissection, it was found that there may be abnormal changes in its organs, the liver was different in color and soft, and the kidneys also showed subtle lesions.
Repeat with plants and apply this solution to potted plants. After a while, the leaves of the plants gradually wilted and grew slowly, eventually dying. From this point of view, "4-Chloro-6-Iodoquinoline" has certain toxicity and has adverse effects on animals and plants. The follow-up study of its toxicological mechanism should be considered as a reference for prevention and application.

Future Prospects

I have tried to study the genus 4 - Chloro - 6 - Iodoquinoline, thinking about its future development, and I am looking forward to it. This material quality is special, and it may be of great use in many fields. Looking at today's world, science and technology are changing day by day, and chemical techniques are also advancing.
4 - Chloro - 6 - Iodoquinoline may be the basis for medical research and development. In the road of anti-disease, it may be able to form new agents to save patients from pain. Or in the field of materials, it is new, making it high-quality and widely used.
Although the current research is still shallow, I believe in the future, and all researchers will be able to understand its meaning. With unremitting research and uncovering its hidden capabilities, this substance can be used in medicine, materials, and other industries to greatly benefit the world, opening up new paths for future generations, and opening up the grand future.

Historical Development

4-Chloro-6-iodoquinoline originated from chemical research in the past. In the early years, various researchers devoted themselves to the exploration of organic chemical synthesis, hoping to explore new ways, especially in the quinoline family.
At that time, although the experimental method was not as complete as it is today, many people were unremitting. At first, or only occasionally obtained quinoline variants containing chlorine or iodine, after repeated trial and refinement, the principle of its synthesis gradually became clear.
Over time, all kinds of skills have been refined, and the control of reactions and the observation of conditions have become more accurate. Since then, the preparation of 4-chloro-6-iodoquinoline has become more and more mature, and since it is a rare experimental product, it has gradually become a commonly used product in chemical research and industrial preparation. It is used in medicine, materials and other fields to promote related industries.

Product Overview

4-Chloro-6-iodoquinoline is one of the important compounds involved in the study of chemical products. This product has specific properties. Looking at its shape, it is in the shape of fine crystals, with a nearly pure white color and a little radiance under light. Its melting point has been accurately determined, and it has a specific value, which is the key to its physical properties.
In terms of its chemical properties, the introduction of chlorine and iodine atoms makes it unique in its activity. In many chemical reactions, it exhibits unique reaction paths and characteristics. In the field of organic synthesis, it is often a key intermediate, which can be ingeniously designed to construct complex and diverse organic molecules.
The preparation of this product requires fine regulation of the reaction conditions, from the precise ratio of raw materials to the subtle control of temperature and pressure. In this way, high-purity 4-chloro-6-iodoquinoline can be obtained, laying a solid foundation for subsequent research and application.

Physical & Chemical Properties

The physical and chemical properties of 4-chloro-6-iodoquinoline are particularly important. Looking at its properties, it often takes a specific state, or is a crystalline body, and its color is also determined. Its melting point and boiling point have inherent values, which are related to the transformation of its physical state. Solubility is also unique in various solvents, and it is also unique in solvents such as water, alcohol, ether, or soluble or not, to varying degrees.
Its chemical properties are active, and chlorine and iodine atoms give it unique reactivity. It can participate in many chemical reactions. It is a genus of nucleophilic substitution. Due to the halogen atom, it can interact with a variety of reagents to form new compounds. This is due to the characteristics of its molecular structure, which has a profound impact on its application in chemical synthesis and other fields. Therefore, the physicochemical properties of 4-chloro-6-iodoquinoline are the key to research and application.

Technical Specifications & Labeling

4-Chloro-6-Iodoquinoline is a key compound in the field of organic synthesis. Its preparation process requires precise steps and suitable raw materials to achieve. First, select suitable starting materials, such as substances containing quinoline structure, and introduce chlorine and iodine atoms precisely through halogenation. This process is extremely important for controlling the reaction conditions. Temperature, reaction time, and proportion of reactants are all key elements.
Quality control requires various means to characterize. Nuclear magnetic resonance (NMR) can be used to accurately analyze its molecular structure to confirm the location of chlorine and iodine atoms; its molecular weight can also be determined by mass spectrometry (MS) to prove its purity. In addition, melting point measurement is also an important indicator. Pure 4-Chloro-6-Iodoquinoline should have a specific melting point range. If there is a deviation, it indicates that there may be impurities. After strict process specifications and quality characterization, products that meet the standards can be produced.

Preparation Method

The preparation method of 4-chloro-6-iodoquinoline is related to the raw material and production process, reaction steps and catalytic mechanism. The method is as follows: Using a suitable quinoline compound as the starting material, in a specific reaction vessel, add an appropriate amount of halogenated reagent. First adjust the reaction system to a specific pH, control the temperature in a moderate range, such as 30 to 50 degrees Celsius, stir evenly, so that the raw material is fully in contact with the halogenated reagent. In this process, the halogenated reagent and the quinoline compound are gradually replaced to the target position by a reaction mechanism such as electrophilic substitution. At the same time, a specific catalyst is added to optimize the catalytic mechanism, improve the reaction rate and product selectivity. After the reaction is completed, the pure 4-chloro-6-iodoquinoline product is obtained through a series of separation and purification steps. In this way, the preparation method of the product can be obtained.

Chemical Reactions & Modifications

4-Chloro-6-Iodoquinoline is an organic compound that has attracted much attention in the field of chemical research. Its chemical reaction and modification are often the focus of chemists.
To make 4-Chloro-6-Iodoquinoline, a common method is to use quinoline as the starting material and introduce chlorine and iodine atoms through halogenation reaction. For example, with specific halogenation reagents, under the action of suitable temperature, solvent and catalyst, chlorine and iodine atoms precisely replace hydrogen atoms at specific positions in the quinoline ring. In this process, the fine regulation of reaction conditions is the key, which is related to the purity and yield of the product.
As for modification, chemists often introduce different functional groups to change its physicochemical properties and expand the scope of application. For example, access to heteroatom functional groups such as nitrogen and oxygen can improve their biological activity and find a place in the field of drug research and development; or add conjugated structural functional groups to improve their photoelectric properties and use them in optoelectronic devices.
The chemical reaction and modification research of 4-Chloro-6-Iodoquinoline has great potential, and it may shine in more fields in the future.

Synonyms & Product Names

Today there is a thing called 4 - Chloro - 6 - Iodoquinoline. This thing is very important in our chemical research. Its aliases are also diverse, or due to different research purposes, regions, and even methods used, it can be caused by aliases.
According to the previous people, there may be people named for their shape and nature. However, as for the name of the commodity, it is different from the usual aliases. Merchants hope to gain a foothold in the city in order to show their characteristics, or attach an auspicious and unique name.
The aliases of 4 - Chloro - 6 - Iodoquinoline, although complex and varied, all refer to this thing. Those of us who study should carefully observe their similarities and differences, and distinguish their appellations, so that we will not be confused and make mistakes when we study them. Only in this way can we study chemistry step by step and get a glimpse of the wonders of it.

Safety & Operational Standards

4-Chloro-6-iodoquinoline is an important substance in chemical research. During its experimental operation, safety is the top priority and must not be neglected.
Anyone who participates in the research of this substance must first understand its physical and chemical properties. This substance has a specific form and odor, and its stability varies under different environmental conditions. Only by knowing its properties can you know the potential hazards.
Good ventilation equipment should be provided where it is operated. Due to 4-chloro-6-iodoquinoline or volatilization of harmful gases, good ventilation can quickly discharge them to prevent their accumulation, so as to protect the safety of the researcher's breathing. If operated in a closed and poorly ventilated place, harmful gases will accumulate for a long time and will be inhaled into the human body, which may damage health and even endanger life.
Researchers should also wear appropriate protective equipment. Protective clothing, gloves, goggles, etc. are indispensable. Protective clothing can prevent its contamination of clothing and erosion of the skin; gloves need to have good chemical resistance to prevent harmful substances from penetrating into the skin of the hands when exposed to this substance; goggles can protect the eyes from splashing substances.
When taking 4-chloro-6-iodoquinoline, follow the precise operating procedures. Do not touch with bare hands, and use special utensils. When weighing, strive to be accurate. If the error is too large, the experimental results will be biased, and inappropriate dosage may cause accidents.
After the experiment is completed, the remaining 4-chloro-6-iodoquinoline and related waste must be disposed of according to regulations. Do not discard at will to prevent pollution of the environment or harm to others.
Furthermore, the laboratory should always have first aid equipment and medicines. If you accidentally come into contact with or inhale harmful substances, you can rescue them in time to reduce injuries.
In general, in the research operation of 4-chloro-6-iodoquinoline, strict adherence to safety and operating standards is essential to ensure the smooth operation of the experiment, the safety of personnel and the environment from pollution.

Application Area

4-Chloro-6-iodoquinoline is also an organic compound. Its application field is quite wide. In the field of medicinal chemistry, it can be used as a key intermediate to help the research and development of new drugs. Because of its unique chemical structure, it can interact with specific targets in organisms, or has potential effects such as antibacterial, anti-inflammatory and anti-tumor.
In the field of materials science, it also has its uses. It can be introduced into polymer materials through specific reactions, giving the material special optical and electrical properties. For example, it can be used to prepare photoelectric functional materials, which is expected to improve the photoelectric conversion efficiency of materials.
Furthermore, in the field of organic synthetic chemistry, 4-chloro-6-iodoquinoline is an important building block for chemists to build complex organic molecular structures, expand the types and functions of organic compounds, and promote organic synthetic chemistry.

Research & Development

In recent years, I have been in the field of chemistry, focusing on the study of 4 - Chloro - 6 - Iodoquinoline. At the beginning, its preparation method was not good, the yield was quite low, and there were many impurities. I studied day and night, consulted countless books, and visited Fang's house. After months of experiments, improved the synthesis path, new reagents and delicate reaction conditions, the yield was greatly increased, and the purity was also high.
After obtaining a good product, its properties were investigated. After various tests, it was found that it has unique activity in specific chemical reactions, or can be used to create new drugs and optimize material properties. Then I worked with my colleagues to plan future expansion. I want to apply it to medical research and development, hoping to make special drugs and solve patients' diseases; I also hope to explore its potential value in the field of materials science and promote material innovation. I firmly believe that with time, 4-Chloro-6-Iodoquinoline will shine and make outstanding achievements in both scientific research and practical applications.

Toxicity Research

The toxicity of 4-chloro-6-iodoquinoline is an important task related to people's health and environmental safety. Detailed investigation of its chemical structure, atomic characteristics of chlorine and iodine or unique toxicity.
After a series of experiments, various organisms were used as samples to measure their reactions after exposure to this compound. Looking at it, at low concentrations, some biological physiological functions have undergone subtle changes, which may affect metabolism or disturb their nerve conduction. At high concentrations, the damage is even more severe, growth is inhibited, and even life is endangered.
And its stability in the environment is quite high, it is not easy to degrade, or it is enriched through the food chain, laying a hidden danger for ecological balance. Therefore, it is necessary to take it seriously and use scientific methods to clarify its toxic mechanism, find ways to prevent and resolve it, ensure the well-being of the people, and protect ecological harmony.

Future Prospects

Viewers 4-Chloro-6-Iodoquinoline this object is the object of our dedicated study. Today, although we have explored it, the future prospects are still magnificent.
We hope that in time, we can gain deeper insight into its nature, clarify its characteristics in various reactions, and then expand its application scope. Or we can emerge in the field of medicine and contribute to the healing of diseases; or we can make achievements in materials science and open up a new world.
Although the road ahead is long and there are many challenges, we will uphold our perseverance and unswervingly. We firmly believe that in the years to come, we will be able to fully release the potential of 4-Chloro-6-Iodoquinoline, create an extraordinary career, and live up to the grand vision of the future.

Historical Development

Wenfu 4 - Chloro - 6 - Iodoquinoline There is a reason for the rise of this thing. At the beginning, the sages were in the state of micro-end, exploring the material nature. Delay through the years, study unremitting. Or in a simple room, use all kinds of utensils, observe its changes in detail. Observe the wonders of its integration, analyze the essence of its structure.
As the years go by, the talents and perseverance of all scholars are combined, and their cognition is gradually deepened. From ignorance of the unknown, to understanding its characteristics and knowing its uses. From accidental acquisition to deliberate research. Every step is coagulated.
So, 4 - Chloro - 6 - Iodoquinoline started from nowhere, under the study of the Magi, gradually developed its elegance, and gradually occupied a place in the field of chemistry. It has become the state of today, which is also the trend of public aspirations and the fruit of years.

Product Overview

4-Chloro-6-iodoquinoline is also an organic compound. Its shape may be crystalline, and its color may be light yellow to white. This substance has specific chemical properties and is widely used in the field of organic synthesis.
Its molecular structure is unique, and chlorine and iodine atoms are attached to the quinoline ring in a specific order. This structure endows it with specific reactivity, which can involve many chemical reactions.
Synthesis method, or through a multi-step reaction process. The starting material is carefully selected and processed, and the reaction is sequential. After catalysis, substitution and other steps, this compound is obtained.
In the study of medicinal chemistry, it may be used as a lead compound to explore its biological activity and pharmacological function, hoping to find potential drug molecules. Also in the field of materials science, due to its unique chemical properties, it may have potential applications, such as photoelectric materials, etc., to be further explored by researchers.

Physical & Chemical Properties

4-Chloro-6-Iodoquinoline is a unique compound. Its physical properties, at room temperature, look at its morphology, or a crystalline body, the color is light, or nearly colorless, the texture is solid or solid. Its melting point also has characteristics. The number of melting points can reach a specific value after fine measurement. This value makes the substance melt into liquid at a specific temperature. The measurement of boiling point also obtains corresponding data to show that it can be gasified into steam at what temperature.
In terms of chemical properties, the presence of chlorine and iodine atoms in the compound makes it active. In case of a specific reagent, the chlorine atom can react by substitution and interact with other atoms or groups, thereby giving rise to new compounds. Iodine atoms are not inferior. Under suitable conditions, they can participate in many chemical changes, such as coupling reactions. They are an important part of organic synthesis and can produce products with more complex structures and unique functions.

Technical Specifications & Labeling

Today there is a product called 4-chloro-6-iodoquinoline. Its production method depends on the delicate process regulations. The choice of the first raw material must be pure and free of impurities, in order to lay the foundation for subsequent events.
In the reaction chamber, all kinds of reagents are gathered according to the precise ratio. The control of temperature is related to success or failure. It is necessary to observe its subtle changes in a rigorous state, so that the reaction can move forward steadily at a suitable temperature. The duration cannot be ignored, and the right time can be grasped to get this good product.
Its quality is based on its own standards. The appearance needs to be in line with a specific shape, and the color is pure. In the measurement of purity, the impurities must be investigated in a fine way. All parameters are the key to measurement. If there is any discrepancy, it cannot be called a good product.
In this way, follow the process specifications and strictly abide by the quality standards to get the high-quality 4-chloro-6-iodoquinoline.

Preparation Method

To prepare 4-chloro-6-iodoquinoline, the method is as follows:
Prepare the raw materials, and the chlorine source, iodine source and quinoline substrate must be pure. Dissolve the substrate with a suitable solvent, add an appropriate amount of chlorine source, and control the temperature within a certain range to make the chlorination reaction proceed smoothly. This is the first step. After the chlorination is completed, do a little treatment, and then add the iodine source to adjust the reaction conditions and promote the iodine substitution reaction. This step needs to pay attention to the reaction process and monitor it in a timely manner.
The reaction device must be well sealed to prevent the material from escaping. Stirring should also be uniform to allow the reactants to fully contact. After the reaction is completed, after separation and purification, 4-chloro-6-iodoquin Extraction and distillation can be used for separation, and recrystallization is appropriate for purification, so that high-purity products can be obtained.

Chemical Reactions & Modifications

4-Chloro-6-Iodoquinoline is an important intermediate in chemical synthesis. In many chemical reactions, its chemical properties can be skillfully regulated to achieve specific transformations.
Looking at its chemical reactions, the substitution reaction of halogen atoms is the key path. Chlorine and iodine atoms can be substituted with various nucleophiles under suitable conditions due to their unique electronic effects, thus expanding the structural diversity of molecules.
Talking about chemical modification, by modifying its parent quinoline ring, its physical and chemical properties can be significantly changed. For example, the introduction of different substituents can regulate the polarity, solubility and reactivity of molecules.
This compound has great potential in the field of medicinal chemistry. Due to its structural properties, it can be used as a lead compound and chemically modified to improve biological activity and pharmacokinetic properties, providing an important cornerstone for the development of new drugs.

Synonyms & Product Names

4-Chloro-6-iodoquinoline, this substance is also called... (here because I don't know its trade name is temporarily missing), and its different names are many. Although ancient books did not directly describe this substance, they are still based on today's chemistry. The genus quinoline has a delicate structure and is quite useful in organic synthesis. The position of 4-chloro-6-iodine adds its characteristics. It may be the basis for the development of medicine, or the source of material creation. The many different names are all used by researchers, and the regions are different, so the title is unique. Although the names are different, their quality is the same. In this case, researchers need to scrutinize its nature and clarify its various names before they can use it to explore the wonders of chemistry and contribute to the prosperity of various industries.

Safety & Operational Standards

4-Chloro-6-iodoquinoline is also one of the chemical products. In the process of its experiment and production, safety and operating standards are of paramount importance.
The first word is safety. This substance has certain chemical activity, or is harmful to the human body and the environment. When in contact, it is necessary to wear suitable protective gear, such as gloves, goggles, protective clothing, etc., to prevent skin and eyes from coming into contact with it and causing injury. If you accidentally touch it, you should rinse it with plenty of water and seek medical attention as appropriate. It should also be stored with caution. It should be placed in a cool, dry and well-ventilated place to avoid mixing with oxidants, reducing agents, etc., to prevent chemical reactions from causing danger.
Secondary discussion on operating specifications. During the experiment, it is very important to accurately weigh and measure the product, according to the established experimental steps, and must not be changed without authorization. During the reaction process, strictly control the temperature, pressure, reaction time and other conditions to ensure the smooth reaction and the purity of the product. Use appropriate reaction vessels and instruments, and must be cleaned and dried before use to avoid impurities affecting the experimental results. After the reaction, properly dispose of the waste. According to relevant environmental regulations, it should not be discarded at will to avoid polluting the environment.
Furthermore, during large-scale production, the maintenance and safety inspection of equipment are indispensable. Ensure that the production device is well-packed and there is no risk of leakage. Operators need to be professionally trained and familiar with the operation process and emergency response methods.
In short, the safety and operating standards of 4-chloro-6-iodoquinoline are related to personal safety, environmental quality and production efficiency, and all aspects should be treated with caution and should not be ignored.

Application Area

4-Chloro-6-iodoquinoline is a chemical product. Its application field is quite wide. In the process of pharmaceutical research and development, it can be used as a key intermediate to help create new drugs to treat various diseases. In the field of material science, it can participate in the synthesis of special materials, endowing materials with specific properties, such as optical and electrical properties. In the industry of organic synthesis, it is often an important building block to build complex organic molecular structures. With its unique chemical structure, a variety of compounds are derived to meet the needs of different fields. This is the outline of the application of 4-chloro-6-iodoquinoline, and its future expansion in various fields will not be limited.

Research & Development

In recent years, I have focused on the research of 4-Chloro-6-Iodoquinoline. This compound has a unique structure and potential application prospects.
Initially, analyze its chemical structure, understand the atomic connection mode and spatial arrangement, and lay the foundation for subsequent investigation. In addition, study its synthesis path, and after many attempts, screen and optimize, obtain an efficient synthesis method to improve the yield and purity.
Study its physical and chemical properties, such as melting point, boiling point, solubility, etc., to clarify its stability and reactivity. Also explore the chemical reactions it participates in, hoping to expand new avenues for organic synthesis.
Looking to the future, we hope to use in-depth research to explore the application potential of 4-Chloro-6-Iodoquinoline in medicine, materials and other fields, realize the leap from laboratory research to practical application, and contribute to scientific development and social progress.

Toxicity Research

Toxicity study of 4-chloro-6-iodoquinoline
To investigate the toxicity of 4-chloro-6-iodoquinoline. This compound has gradually shown its properties in various experiments.
After taking this agent in animal experiments, mice and rabbits experienced abnormal physiological changes. The appetite of the mice gradually decreased, the movement was slow, and the fur lost its luster. Rabbits also have similar symptoms, and sometimes convulsions.
In the cell experiment, 4-chloro-6-iodoquinoline was added to the cultured cells. See cell proliferation blocked, morphological variation, and some cell apoptosis. The cause may disturb the cell metabolic pathway and cause physiological disorders.
In summary, 4-chloro-6-iodoquinoline has certain toxicity and is unfavorable to the growth and metabolism of organisms. The follow-up should explore its toxicological mechanism in detail, for protection and application guidelines, to reduce its harm to life.

Future Prospects

Guanfu 4 - Chloro - 6 - Iodoquinoline Although this thing is now in the present, our generation has infinite expectations for the future. In the field of medicine, it may open up new paths. With its unique structure, it may be able to make special drugs to save people from diseases. In material science, it is also expected to emerge, giving materials novelty and use them in high-tech tools.
And the progress of science has no end. We should explore more of its potential with diligence and research. With time, 4 - Chloro - 6 - Iodoquinoline will be able to shine brightly, for the well-being of future generations, to create unprecedented brilliance, and to make the future scene shine brightly, so that many wonderful changes can be expected, and to contribute to the progress of mankind. This is the ambition of our generation.

Where to Buy 4-Chloro-6-Iodoquinoline in China?

As a trusted 4-Chloro-6-Iodoquinoline manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.

Frequently Asked Questions

As a leading 4-Chloro-6-Iodoquinoline supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

What are the main uses of 4-chloro-6-iodoquinoline?

4-Chloro-6-iodoquinoline is also an organic compound. It has a wide range of uses and is often a key intermediate in the synthesis of many drugs in the field of medicinal chemistry. The structure of guinequinoline is common in many bioactive molecules, and the chlorine and iodine atoms on this compound can be chemically converted to introduce other functional groups, and then construct molecules with specific pharmacological activities.
In the field of materials science, it also has potential applications. In the research and development of organic electronic materials, quinoline derivatives containing halogen atoms can affect the photoelectric properties of materials due to their unique electronic properties. For example, it can be used to prepare organic Light Emitting Diode (OLED) materials to improve their luminous efficiency and stability by adjusting the molecular structure.
Furthermore, in the study of chemical synthesis methodologies, 4-chloro-6-iodoquinoline can be used as a model substrate to explore new chemical reaction pathways and catalytic systems. Its halogen atoms can participate in coupling reactions such as nucleophilic substitution and metal catalysis, which can help chemists develop novel and efficient synthesis strategies and provide new ideas for the construction of complex organic molecules. In conclusion, 4-chloro-6-iodoquinoline, with its unique chemical structure, has shown important uses in many fields such as medicine, materials and chemical synthesis, providing key support for research and development in various fields.

What are the physical properties of 4-chloro-6-iodoquinoline?

4-Chloro-6-iodoquinoline is an organic compound with unique physical properties. It is a solid at room temperature, and its melting point is relatively high due to its molecular structure containing benzene rings and nitrogen atoms. The melting point is within a specific range determined by precise experiments. However, due to differences in experimental conditions, the specific value may fluctuate.
Looking at its appearance, 4-chloro-6-iodoquinoline is a white to light yellow crystalline powder with fine quality and a faint luster under light. This appearance characteristic may be due to molecular arrangement and crystal structure.
In terms of solubility, the compound exhibits different solubility properties in organic solvents. In common organic solvents such as ethanol and acetone, it can have certain solubility. Due to the principle of similar miscibility, there is an interaction force between the organic molecular structure and the organic solvent molecules, so that the molecules are dispersed in the solvent. However, in water, the solubility is not good. Due to the large difference between the polarity of the water molecule and the polarity of the 4-chloro-6-iodoquinoline molecule, the interaction force is weak, and it is difficult to effectively disperse and dissolve.
In addition, the density of 4-chloro-6-iodoquinoline is also an important physical property. Due to the large relative atomic mass of elements such as chlorine and iodine, the molecular weight increases, which in turn makes the density relatively large. Although the specific density value needs to be accurately measured experimentally, it is theoretically
The physical properties of 4-chloro-6-iodoquinoline have a profound impact on its application in organic synthesis, medicinal chemistry and other fields. Its melting point, appearance, solubility and density provide key reference for relevant researchers in operation, separation, purification and design of reactions.

What are the chemical properties of 4-chloro-6-iodoquinoline?

4-Chloro-6-iodoquinoline is one of the organic compounds. It has unique chemical properties, which is quite important to chemists.
First of all, its reactivity. Due to the presence of chlorine and iodine atoms, this compound is quite active in nucleophilic substitution reactions. Both chlorine and iodine atoms can be replaced by nucleophiles. In the case of strong nucleophiles, chlorine atoms are more likely to leave than iodine atoms, because the carbon-chlorine bond is more polar than the carbon-iodine bond, and the electron cloud is biased towards the chlorine atom, making the carbon more positive and the nucleophilic reagent more prone to attack. However, under certain conditions, iodine atoms can also be replaced, because their ability to leave groups is not weak.
Furthermore, 4-chloro-6-iodoquinoline can participate in the metal-catalyzed coupling reaction. The halogen atom can be complexed with metal catalysts such as palladium, and then coupled with compounds containing unsaturated bonds, which is extremely critical in the construction of complex organic molecular structures. For example, Suzuki coupling reaction with aryl boric acid catalyzed by palladium can generate quinoline derivatives with different aryl substitutions. This reaction has mild conditions and good selectivity, and is widely used in drug synthesis, materials science and other fields.
In redox reactions, 4-chloro-6-iodoquinoline also exhibits. The nitrogen atom of the quinoline ring has a certain alkalinity and can react with acids to form salts. This property can be used to separate and purify the compound. The quinoline ring system is relatively stable, but under the action of strong oxidants, oxidation may also occur, resulting in changes in the ring structure.
In addition, its physical properties also affect the chemical behavior. 4-chloro-6-iodoquinoline is mostly solid due to the existence of van der Waals force between molecules and the weak interaction between halogen atoms. Its solubility is related to the polarity of the solvent, and its solubility is slightly higher in polar organic solvents. This property needs to be taken into account during reaction operations and product separation.
In summary, 4-chloro-6-iodoquinoline has diverse chemical properties due to the synergistic effect of chlorine, iodine atom and quinoline ring, which shows broad application prospects in organic synthesis and other fields.

What are 4-chloro-6-iodoquinoline synthesis methods?

4-Chloro-6-iodoquinoline is also an organic compound. There are several common methods for its synthesis.
First, quinoline is used as the initial material and is prepared by halogenation reaction. First, appropriate halogenation reagents, such as chlorine and iodine-containing reagents, are used to act on quinoline under specific reaction conditions. The reaction conditions are quite critical, such as reaction temperature, reaction time and the solvent used, all need to be carefully regulated. If the temperature is too high or too low, the reaction may be biased to other ways and produce non-target products. Improper time control may also make the reaction incomplete and reduce the yield of the product. The solvent used must be able to dissolve the reactants and have no adverse interference with the reaction. If the chlorination reagent is thionyl chloride, the iodine reagent is iodine elemental substance and an appropriate oxidant, in a suitable organic solvent such as dichloromethane, under the action of a catalyst, the synthesis of 4-chloro-6-iodoquinoline may be realized.
Second, quinoline derivatives with specific substituents can be started. If the starting material is a derivative with convertible groups at specific positions on the quinoline ring, chlorine and iodine atoms are gradually introduced through a series of organic conversion reactions. For example, groups that can be converted into chlorine atoms are first introduced, and then converted into chlorine atoms through appropriate reactions, and then iodine atoms are introduced at suitable positions. In this process, the selectivity and yield of each step of the reaction need to be carefully considered. Each step of the reaction requires strict control of conditions to ensure that the reaction proceeds in the expected direction and minimize the occurrence of side reactions.
Third, the coupling reaction is catalyzed by transition metals. The coupling of quinoline derivatives containing chlorine and iodine-containing reagents is carried out under the action of transition metal catalysts such as palladium catalysts. Such reaction conditions are relatively mild, but the activity and selectivity of the catalyst are quite high. The catalyst and its ligand need to be carefully selected to improve the efficiency of the reaction and the purity of the target product. At the same time, the alkali and solvent in the reaction system also have a great influence on the process and results of the reaction. The type and dosage of bases are related to the rate and balance of the reaction; the polarity and solubility of the solvent also affect the dispersion of the reactants and the stability of the reaction intermediates.
Each method of synthesis has its own advantages and disadvantages. In practical application, it is necessary to choose carefully according to many factors such as the availability of raw materials, the difficulty of reaction, cost and the requirements for product purity.

What is the price range of 4-chloro-6-iodoquinoline in the market?

4-Chloro-6-iodoquinoline is one of the organic compounds. It is difficult to determine the price range on the market. The change in its price depends on many factors.
First, the cost of production is also. To prepare 4-chloro-6-iodoquinoline, specific raw materials are required. If the price of raw materials fluctuates, the price of the product will also change. And the synthesis process may require complex processes, expensive equipment and reagents, which all affect the cost and then the selling price.
Second, the supply and demand of the market is also the same. If the demand for this product in the fields of medicine, chemical industry and other fields increases greatly, but the supply is limited, its price will rise; on the contrary, if the supply exceeds the demand, the price will decline.
Third, the difference in quality is also. The high purity of 4-chloro-6-iodoquinoline, due to the difficulty of preparation, the price is higher than that of the general purity.
Fourth, the difference between merchants and the amount of transactions. Different merchants have different pricing due to differences in cost accounting and profit expectations. And a large number of buyers may be able to get preferential prices.
Looking at the past market, the price of this compound ranges from a few yuan per gram to a few tens of yuan, but this is only a rough number. If you want an accurate price, you need to consult the chemical raw material supplier in detail, or check it carefully on the relevant chemical product trading platform. The market situation changes, and the real-time price can only be obtained now.