4 Pyridinecarboxaldehyde 3 5 Dimethoxy
pyridine pyrrole pyrazine piperidine piperazine

4-pyridinecarboxaldehyde, 3,5-dimethoxy-

    Specifications

    HS Code

    589934

    Chemical Formula C9H11NO3
    Molar Mass 181.19 g/mol
    Appearance Solid (usually)
    Odor May have a characteristic odor
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Limited solubility
    Solubility In Organic Solvents Soluble in some organic solvents
    Density Data needed
    Pka Data needed
    Stability Should be stored properly to maintain stability
    Hazard Class Data needed

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    General Information
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    Frequently Asked Questions

    As a leading 4-pyridinecarboxaldehyde, 3,5-dimethoxy- 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 physical properties of 4-pyridyl formaldehyde, 3,5-dimethoxy -?
    4-Ethylheptanal and 3,5-diethoxy-have their own characteristics.
    First of all, 4-ethylheptanal, its outer surface is often transparent to light color liquid. Smell, with a special aldehyde fragrance, this fragrance has a degree of discrimination, or it can be slightly fruity sweet, but also has the unique flavor of aldehyde. The boiling temperature depends on the molecular force and other factors, roughly at a certain degree of temperature. Due to the existence of aldehyde groups in the molecule, it has a certain degree of solubility, so it has good solubility in soluble solutions such as ethanol and acetone; non-soluble solutions such as hexane, solubility is good. In terms of density, the water is slightly dense and floats on the water. Due to the formation and arrangement of atoms by molecules, the amount of water is small.
    Re-3,5-diethoxy -, often under or solid, or due to the shadow of substituents and molecular integrators, it is a viscous liquid. The melting force of the molecules is closely related, including Vander force, etc. Due to the existence of ethoxy groups, the molecular properties have been changed, and their solubility is also very low. In the solution of alcohols, the solubility of ethoxy alcohols can be reduced due to the formation of interactions such as alcohol. In water, the ethoxy group has a certain water content, but due to molecular integrators and other factors, the solubility may be limited. Its density also depends on the formation of molecules, or the density of similar compounds is similar. The physical properties of the two are determined by their molecular properties, and the differences between them are different. In fields such as chemical research and engineering, they all have different uses due to these characteristics.
    What are the chemical properties of 4-pyridyl formaldehyde, 3,5-dimethoxy -
    The chemical properties of 4-dimethyl ether, 3,5-diethoxy are related to the characteristics of this compound in various chemical situations. This substance has the common properties of ether compounds.
    In terms of physical properties, it generally appears as a liquid state with a specific boiling point and melting point. Due to the existence of ethoxy and methyl ether groups between molecules, the intermolecular forces present a specific situation, so its boiling point may be affected by this. Ether compounds are usually relatively stable at room temperature and pressure, and their solubility in water is limited. This is due to their weak molecular polarity and weak interaction with water molecules.
    From the perspective of chemical properties, the etheric bond (-O-) is an important structural feature. This bond can be broken under certain conditions. For example, in a strong acid environment, the protonation of the ether bond may be initiated, which may lead to the fracture of the ether bond, resulting in the formation of corresponding products such as alcohols or halogenated hydrocarbons.
    Furthermore, the presence of 3,5-diethoxy groups changes the electron cloud density on the benzene ring. Ethoxy groups act as power supply groups, which will increase the electron cloud density of the benzene ring, making the benzene ring more prone to electrophilic substitution reactions. Common electrophilic substitution reactions, such as halogenation reactions, nitrification reactions, sulfonation reactions, etc., may be easier to carry out on this compound, and the reaction check point may be affected by the localization effect of ethoxy groups, which tends to be substituted at specific positions on the benzene ring.
    In addition, although the methyl ether group in this compound is relatively stable, it may be oxidized under the action of some strong oxidants, but compared with the easily oxidized functional groups such as aldodes and ketones, the oxidation conditions may be more severe. In short, the chemical properties of 4-dimethyl ether and 3,5-diethoxy are determined by its unique molecular structure. It has certain research value and application potential in the fields of organic synthesis and chemical reaction mechanism research.
    4-Pyridyl formaldehyde, 3,5-dimethoxy - is used in what fields?
    4-Ethylheptane and 3,5-diethoxy have been used in many fields for a long time, and they are actually the products of natural and artificial ingenious combination.
    In the field of medicine, 4-ethylheptane can be used as a key intermediate for the synthesis of specific drugs. Ancient healers, when seeking a cure for diseases, investigated the characteristics of various substances in detail. Although the exact structure was unknown at that time, after repeated attempts, it has been found that substances containing such structures may have a alleviating effect on diseases. Today, with technological advancements, doctors can accurately integrate them into drug synthesis pathways according to their chemical properties, making drugs more effective. 3,5-Diethoxy is also often found in pharmaceutical ingredients, which can adjust the solubility and stability of drugs, just like what was added when processing drugs in ancient times, which can make the effect of drugs better.
    In the fragrance industry, 4-ethylheptane can give fragrances a unique smell and add a different touch to fragrances. In the past, people made incense, emphasizing the fusion of natural aromas. Although the name of this compound is not known, when mixed with natural raw materials, ingredients containing 4-ethylheptane may have been incorporated into it. As for 3,5-diethoxy, it can create a gentle and lasting fragrance, just like the ancient incense, pursuing the long and pleasant aroma, and it also plays a key role in the preparation of fragrances.
    In the field of organic synthesis, 4-ethylheptane and 3,5-diethoxy are both important raw materials and reagents. Organic synthesis, like ancient artisan creations, requires precise grasp of the characteristics of various materials. Chemists use it as a basis to construct complex organic molecular structures and synthesize many materials with special properties, which are widely used in paints, plastics and other industries. Just like the ancients created exquisite utensils with simple materials to meet different needs.
    What is the preparation method of 4-pyridine formaldehyde, 3,5-dimethoxy -?
    To prepare 4-aminobenzoic acid, 3,5-diethoxyl-, you can do it according to the following method.
    First take appropriate starting materials, such as compounds containing corresponding functional groups. It is better to have a benzene ring and a group that can be converted into a target functional group in an appropriate position. A specific substitution reaction can be carried out on the benzene ring to introduce an ethoxy group. For example, using phenolic compounds as starting materials, reacting with halogenated ethane under basic conditions, using the nucleophilic substitution reaction mechanism, the oxygen anion of the hydroxyphenol group launches a nucleophilic attack on the carbon atom of the halogenated ethane, and the halogen ion leaves, thereby introducing an ethoxy group on the benzene ring to obtain a benzene derivative containing 3,5-diethoxy. < Br >
    Then, consider introducing an amino group. The method of nitro reduction can be used. First, the nitro group is introduced at a suitable position in the benzene ring by nitrification reaction. The mixed acid of concentrated sulfuric acid and concentrated nitric acid is used as the nitrifying reagent. The benzene ring undergoes an electrophilic substitution reaction under the action of mixed acid, and the nitro cation acts as the electrophilic reagent to attack the benzene ring to generate 3,5-diethoxybenzene derivatives containing nitro groups. After
    , the nitro group is reduced to an amino group. The commonly used method is catalytic hydrogenation, with palladium carbon as the catalyst, and the nitro group is gradually reduced to an amino group in a hydrogen atmosphere. Or use chemical reduction method, such as iron filings and hydrochloric acid as reducing agents, nitro can also be reduced to amino groups in this system, and the final product is 4-aminobenzoic acid and 3,5-diethoxy-product.
    During the reaction process, attention should be paid to the precise control of the reaction conditions. Temperature, reaction time, reagent dosage and other factors have a significant impact on the yield and selectivity of the reaction. And after each step of the reaction, it is advisable to separate and purify through suitable means, such as recrystallization, column chromatography, etc., to obtain pure intermediate products and final products to ensure the smooth progress of the reaction and the quality of the products.
    What is the market outlook for 4-pyridyl formaldehyde, 3,5-dimethoxy -?
    Hearing your inquiry, it is also related to the market prospects of 4-aminobutyric acid and 3,5-diethoxy. These two have their own potential in today's market and cannot be ignored.
    First of all, 4-aminobutyric acid has a wide range of uses in the field of medicine. It can help sleep and calm the nerves and relieve anxiety, so in the health care market, the demand is growing. Today's people are often trapped by stress, and there are more and more sleep and emotional diseases. 4-aminobutyric acid, with its natural soothing ability, meets the needs of the public, and the market prospect is promising. And it can also be added to food, such as the development of functional drinks, which can stimulate a consumption boom. In agriculture, it can also be used as a plant growth regulator to improve crop resistance, which opens up new avenues, and the potential of the market needs to be dug deeper.
    As for 3,5-diethoxy group, a genus of chemical raw materials, it is a key component of many fine chemicals. In the industry of coatings and inks, it can increase its performance, make the coating uniform, fresh color, and good durability. When the construction, automotive and other industries are booming, the demand for coatings and inks is on the rise, and 3,5-diethoxy group is also benefited by it, and the dosage is increasing. In the process of pharmaceutical synthesis, as an important intermediate, pharmaceutical research and development continues, and new drugs are emerging, and its demand also rises.
    However, the market is changing, and both are also facing challenges. The rise of competing products and changes in regulations all need to be dealt with. However, looking at the general trend, 4-aminobutyric acid is widely used in health and agriculture, and 3,5-diethoxy is important in chemical and pharmaceutical industries. If you can properly observe the market and study technology, you will be able to win a place in the city, and the prospect is promising.