3 5 Dichloropyridine 4 Carbaldehyde
pyridine pyrrole pyrazine piperidine piperazine

3,5-dichloropyridine-4-carbaldehyde

    Specifications

    HS Code

    573491

    Chemical Formula C6H3Cl2NO
    Molar Mass 176.00 g/mol
    Appearance Solid
    Color Typically white to off - white
    Odor Characteristic organic odor
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Melting Point 93 - 95 °C

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    General Information
    Where to Buy 3,5-dichloropyridine-4-carbaldehyde in China?
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    Frequently Asked Questions

    As a leading 3,5-dichloropyridine-4-carbaldehyde 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 3,5-dichloropyridine-4-formaldehyde?
    3,2,5-Dihydroxybenzene-4-methoxyacetophenone has a wide range of uses. In the field of medicine, it can be used as a key intermediate to help synthesize a variety of drugs. For example, in the preparation process of some compounds with specific pharmacological activities, 3,2,5-Dihydroxybenzene-4-methoxyacetophenone can provide key structural units for the reaction by virtue of its unique chemical structure, thereby promoting the construction of target drug molecules, or affecting the efficacy and stability of drugs.
    In the field of materials science, it can participate in the creation of functional materials. Because its functional groups can undergo specific chemical reactions with other substances, they can be introduced into polymer materials and other systems, endowing materials with new properties, such as changing the optical properties, electrical properties or enhancing the stability of materials, etc., opening up new paths for the research and development of new materials.
    In the field of organic synthesis, 3,2,5-dihydroxybenzene-4-methoxyacetophenone plays a cornerstone role. It can be combined with various reagents through a series of organic reactions to derive organic compounds with diverse structures, which greatly enriches the library of organic compounds and contributes to the development of organic synthetic chemistry. No matter whether it is to build complex natural product analogs or design novel organic molecular structures, it may be used as a starting material or a key intermediate to start the synthesis journey.
    What are the synthesis methods of 3,5-dichloropyridine-4-formaldehyde?
    The synthesis method of 3,5-dihydroxybenzoic acid-4-methyl ether is related to the delicate skills of organic chemistry. This article describes its common synthesis methods for those who seek knowledge.
    First, it can be extracted from natural products and then modified. Many plants contain compounds with similar structures. The initial raw materials are obtained through extraction, separation, purification and other steps, and then chemically modified, such as methylation reaction, methoxy group is introduced to obtain 3,5-dihydroxybenzoic acid-4-methyl ether. Although the raw materials are natural, the extraction process is complicated and the yield may not be very high.
    Second, benzoic acid derivatives are used as starting materials. The hydroxyl group can be introduced at a specific position of the benzene ring of benzoate first, and the electrophilic substitution reaction of phenolic compounds is commonly used, which is achieved through a series of steps such as halogenation and hydrolysis. After the hydroxyl group is positioned correctly, the methylation operation is carried out. This step usually selects methylating reagents such as iodomethane and dimethyl sulfate, and reacts under alkali catalysis to obtain the target product. The raw materials in this way are easy to obtain, and the reaction steps are relatively clear, but the reaction conditions of each step need to be precisely controlled to ensure the purity and yield of the product.
    Third, the Diels-Alder reaction strategy is used. Select suitable dienes and dienes, and construct the basic skeleton of the benzene ring through cyclization addition reaction. Subsequent functional group conversion is used to introduce hydroxyl and methoxy groups. This method can efficiently construct complex cyclic structures, but it requires strict reaction substrates and special reaction conditions, which can be carried out smoothly under high temperature or specific catalyst action.
    All this synthesis method has its own advantages and disadvantages. In practical applications, when considering the availability of raw materials, cost considerations, product purity requirements and many other factors, in order to find the optimal synthesis path, the delicate creation of this organic compound can be achieved.
    What are the physical and chemical properties of 3,5-dichloropyridine-4-formaldehyde?
    3,5-Dinitro-4-methoxypyridine, this is an organic compound. Its physical and chemical properties are quite characteristic, let me explain in detail for you.
    Looking at its physical properties, under normal conditions, this compound is mostly solid. Its melting point has a specific value due to the interaction between atoms in the molecular structure, which is crucial for determining the purity and characteristics of the compound. Its solubility is also worthy of attention, and it varies in different solvents. In polar organic solvents, such as ethanol, acetone, etc., due to the polarity of nitro and methoxy groups in the molecule, it can show a certain solubility. Due to the principle of "similar miscibility", polar molecules are easily soluble in polar solvents. However, in non-polar solvents, such as n-hexane, benzene, etc., the solubility is poor.
    As for the chemical properties, the nitro group of 3,5-dinitro-4-methoxypyridine is extremely reactive. Nitro is a strong electron-absorbing group, which can reduce the electron cloud density on the pyridine ring, making the pyridine ring more susceptible to nucleophilic attack. For example, when encountering nucleophilic reagents, such as sodium alcohol, amines, etc., nitro ortho or para-carbon atoms are prone to nucleophilic substitution reactions with them. Although methoxy is a donator group, its effect is slightly weaker than that of nitro. This compound is also sensitive to redox reactions. Nitro groups can be reduced to amino groups under appropriate conditions, which is often used in organic synthesis to introduce amino functional groups to prepare a variety of nitrogen-containing compounds. Due to its structure containing heteroatoms such as nitrogen and oxygen, it can also participate in coordination chemistry-related reactions under specific conditions to form complexes with metal ions. This property may have potential applications in the fields of materials science and catalysis.
    What is the price range of 3,5-dichloropyridine-4-formaldehyde in the market?
    3,5-Dihydroxybenzoic acid-4-methyl ether is available in the market, and its price range varies, depending on quality, supply and demand, and time and place.
    If its quality is pure and refined, and it is made by good methods, without impurities and flaws, and there are many people in the market who want it, and the supply is thin, the price will be high. Its price may range from tens of gold to hundreds of gold per catty.
    However, if the quality is uneven, mixed with other things, and the system is not good, and it is worth oversupply, the price will drop. Or only a few gold spectra per catty.
    It varies from time to time, and the price is also different. In the city of Duhui, merchants converge, and those who seek are easy to gather, and the price may be a little high; in remote places, transportation is inconvenient, and those who seek are few, and the price may be a little low. And when the age is rich, I apologize, and the government is relaxed, all of which are related to the price. In order to know the exact price, when visiting merchants in various cities and scrutinizing the situation at that time, you can get it.
    What are the storage conditions for 3,5-dichloropyridine-4-formaldehyde?
    For 3,5-dihydroxybenzoic acid-4-methyl ether, the stored parts are especially important. This kind of material should be placed in a place where it is dry, dry and good.
    It is important to avoid the harm of high temperature. If it is exposed to heat, its molecules may be damaged due to energy loss, causing its properties to be changed and its original efficacy to be lost. And high temperature is easy to cause it to be reversed and reversed, so that it will not be damaged.
    In the environment of dryness, prevent it from being damp. If water invades, or causes hydrolysis, it will be destroyed and transformed, resulting in effectiveness. It is also damp and prone to microorganisms such as molds, polluting its properties.
    It is good to pass the goods around it, so that it can be scattered and gathered, so as to prevent it from being stained by bad conditions. And it can help to protect the dryness and reduce the severity of the environment.
    It is also necessary to avoid direct light. Light, especially ultraviolet light, has energy, which can stimulate the reaction and make it disappear. Therefore, it is advisable to use opaque devices, such as brown glass bottles, which can block part of the light and reduce its performance.

    It is also important to pay attention to the separation of other things. Different materials, chemical products, or due to the reaction of the phase, causing it to fail, or even produce harmful things. Therefore, be careful to keep this general product in order to obtain the properties of 3,5-dihydroxybenzoic acid-4-methyl ether and ensure its effectiveness.