2 6 Dichloro 5 Fluoropyridine 3 Carbonyl Chloride
pyridine pyrrole pyrazine piperidine piperazine

2,6-dichloro-5-fluoropyridine-3-carbonyl chloride

    Specifications

    HS Code

    133582

    Chemical Formula C6HCl2FNOCl
    Molecular Weight 228.43
    Appearance Typically a solid or liquid, color may vary
    Odor Pungent odor likely due to carbonyl chloride group
    Melting Point Data may vary, needs experimental determination
    Boiling Point Data may vary, needs experimental determination
    Solubility Soluble in some organic solvents, limited in water
    Density Data may vary, needs experimental determination
    Reactivity Highly reactive, especially with nucleophiles
    Hazard Class Corrosive, may cause burns to skin and eyes

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    General Information
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    Frequently Asked Questions

    As a leading 2,6-dichloro-5-fluoropyridine-3-carbonyl chloride 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 2,6-dichloro-5-fluoropyridine-3-formyl chloride?
    2% 2C6-difluoro-5-methoxypyrimidine-3-formaldehyde, which was not available in the era of "Tiangong Kaiwu". However, from today's perspective, it has a wide range of uses.
    In the field of pharmaceutical chemistry, it is an important intermediate in organic synthesis. It can introduce specific functional groups through a series of chemical reactions to build complex chemical structures and be used to create new drugs. For example, for specific disease targets, design and synthesize compounds with unique pharmacological activities, bringing new opportunities for drug research and development, or to optimize the molecular structure of existing drugs, improve efficacy and reduce side effects.
    In the field of pesticide chemistry, compounds with high insecticidal, bactericidal or herbicidal properties can be derived. After reasonable modification, the molecules are highly selective and biologically active to specific pests, pathogens or weeds, providing safer and more efficient pesticide products for agricultural production, helping to increase crop production and reduce pest infestation.
    Although this object is not included in "Tiangong Kaiwu", it is deduced from the spirit of exploration and utilization of all things in ancient times. If born in this world, the ancients would also study and utilize its various uses to serve people's livelihood and promote production. Just as the excavation and application of many materials and processes in "Tiangong Kaiwu" is to meet the needs of life and production, and constantly explore and innovate.
    What are the synthesis methods of 2,6-dichloro-5-fluoropyridine-3-formyl chloride?
    To prepare 2,6-difluoro-5-formyl-3-methoxypyridine, there are many methods, which can be carried out according to different routes and raw materials.
    First, the pyridine derivative with appropriate substituents is used as the starting material, and fluorine atoms are introduced by halogenation reaction. Suitable halogenating reagents can be selected, and under suitable reaction conditions, the pyridine ring is halogenated at a specific position to obtain fluorine-containing pyridine intermediates. After formylation, formyl groups are introduced into the pyridine ring. The choice of formylating reagents and conditions depends on the structure of the intermediate and the reaction characteristics. Then through the methoxylation step, with appropriate methoxylation reagents, under specific reaction conditions, methoxy groups are introduced to achieve the synthesis of the target product.
    Second, benzene derivatives containing different substituents are used as starting materials to construct pyridine rings through multi-step reactions. First, the benzene ring is properly substituted, and the functional groups required to construct the pyridine ring and the target substituent are introduced. After cyclization, benzene derivatives are converted into pyridine derivatives. This process requires precise control of reaction conditions and reagent dosage. After cyclization, the pyridine ring is modified through halogenation, formylation, methoxylation and other steps to obtain 2,6-difluoro-5-formyl-3-methoxy pyridine.
    Third, it can also start from simpler small molecule raw materials and gradually build the target molecular structure through multi-step reactions. After rational design and connection of multi-step reactions, with small molecules as the basis, through addition, substitution, cyclization and other reactions, pyridine rings are constructed and fluorine atoms, formyl groups, methoxy groups and other substituents are introduced. Although this path is complicated, the raw materials are simple and easy to obtain, which has unique advantages.
    Each synthetic method has its own advantages and disadvantages. In practical application, it is necessary to comprehensively consider factors such as raw material cost, reaction conditions, yield, selectivity and difficulty of subsequent separation and purification, and choose the most suitable synthetic route to efficiently synthesize 2,6-difluoro-5-formyl-3-methoxypyridine.
    What are the physical properties of 2,6-dichloro-5-fluoropyridine-3-formyl chloride?
    2% 2C6-difluoro-5-methoxypyridine-3-methyl fluoride, although this substance is not contained in Tiangong Kaiwu, its physical properties can be described as follows in terms of current chemical knowledge:
    It may be in a liquid state at room temperature, because it contains fluorine, methoxy and other groups, and the intermolecular force has its unique features. Looking at its boiling point, due to the high electronegativity of fluorine atoms, the intermolecular force is formed, and methoxy groups can participate in weak interactions, so the boiling point may be slightly higher than that of general pyridine derivatives. However, the specific value needs to be accurately determined by experiments. < Br >
    When it comes to melting point, due to the limited regularity of its molecular structure and the influence of the spatial distribution of fluorine atoms and methoxy groups, the lattice energy is not extremely high, and the melting point may not be very significant. It is estimated that the relatively low temperature range, or near normal temperature, but the exact melting point also depends on experimental investigation.
    Its density is related to the molecular mass and the way of packing. The relative molecular mass of the molecule is increased due to the fluorine atom, and the structure is compact, so the density is slightly larger than that of common organic liquids. The specific value depends on the experimental measurement.
    In terms of solubility, it is slightly soluble in water due to the hydrophilicity of the methoxy group; it is also an organic compound, which may have good solubility in common organic solvents such as ethanol, ether, dichloromethane, etc. According to the principle of similar phase solubility, the force between the organic solvent and the compound molecules is adapted, which is favorable for dissolution.
    In appearance, it may be a colorless to light yellow transparent liquid, and its color is not dark due to the absence of too many conjugated systems in the structure. And the substance may be volatile and may have a slight odor in the air. However, the odor properties are due to the combined action of various groups in the molecular structure, and the actual smell perception is required. When smelling, it should be handled carefully according to the experimental specifications to prevent health hazards.
    What are the precautions for storing and transporting 2,6-dichloro-5-fluoropyridine-3-formyl chloride?
    2% 2C6-difluoro-5-vinyl-3-methoxypyridine should pay attention to the following matters during storage and transportation:
    First, when storing, choose the place carefully. It should be selected in a cool, dry and well-ventilated place, away from fire and heat sources. This is because the substance may be flammable, and it is easy to cause danger in case of open flames and hot topics. If the storage environment temperature is too high, or its volatilization accelerates, the concentration will accumulate in the air, increasing the risk of fire and explosion; if the environment is humid, or reacts with water vapor, its quality will be damaged.
    Second, it should be stored separately from oxidants, acids, bases, etc., and should not be mixed. Because of its active chemical properties, contact with these substances, or trigger violent chemical reactions, and even explode. For example, when it encounters a strong oxidizing agent, or triggers an oxidation reaction, it is dangerous to lose control of the reaction.
    Third, the storage container should also be paid attention to, and it must be tightly sealed. First, to prevent it from evaporating and escaping, polluting the environment and endangering human health; second, to avoid the intrusion of external substances, affecting its purity and stability. The material of the container used also needs to be suitable, and it cannot chemically react with the substance.
    Fourth, during transportation, it is necessary to ensure that the container does not leak, collapse, fall, or damage. The means of transportation need to be equipped with corresponding fire protection and explosion-proof facilities. The speed of the vehicle during transportation should not be too fast, so as to avoid sudden braking to prevent the container from During loading and unloading, the operation should be light and light, and it is strictly forbidden to drop, touch, or bump to prevent damage to the packaging and containers.
    Fifth, transportation and storage personnel must undergo professional training to be familiar with the characteristics, hazards, and emergency treatment measures of the substance. In the event of a leak and other accidents, they can respond quickly and correctly to reduce the harm.
    What are the market prospects for 2,6-dichloro-5-fluoropyridine-3-formyl chloride?
    Today, there are 2,6-dihydro-5-ene to its-3-methoxylene related market prospects, and I will analyze them in detail.
    In the field of Guanfu medicine, this compound may have unique pharmacological activities. Because of its special structure, or can play a role in specific targets, it provides an opportunity for the development of new drugs. In the process of innovative drug creation, researchers often look for compounds with unique structures to find new therapeutic methods. If this 2,6-dihydro-5-ene to its-3-methoxylene can show good biological activity and safety, pharmaceutical companies must pay attention, and the market prospect may be even broader.
    Within the scope of material chemistry, it may be used as a key intermediate for functional materials. By chemical modification, materials can be endowed with special optical, electrical or mechanical properties. Today, the high-tech industry has an increasing demand for materials with special properties. If this compound is used as a basis to develop materials that meet the needs, it has application potential in electronics, optics and other fields, and the market demand is expected to grow gradually.
    However, its market prospects also pose challenges. The process of synthesizing this compound may be complex and costly. If the process cannot be optimized to reduce costs, it will be hindered in large-scale production and marketing activities. Moreover, strict regulations in the fields of medicine and materials require many tests and approvals, which is time-consuming and laborious. This is also an obstacle to entering the market.
    Overall, if 2,6-dihydro-5-ene to its-3-methoxy-ene can overcome the difficulties of synthesis and regulations, it will have considerable market prospects in the fields of medicine and materials, and is expected to emerge in the future market. However, the road ahead still needs to be worked out.