3 5 Dimethyl 2 Hydroxymethyl 4 Methoxypyridine
pyridine pyrrole pyrazine piperidine piperazine

3,5-Dimethyl-2-Hydroxymethyl-4-Methoxypyridine

    Specifications

    HS Code

    225702

    Chemical Formula C8H13NO3
    Molar Mass 171.194 g/mol
    Appearance Solid (predicted)
    Boiling Point Estimated value
    Melting Point Estimated value
    Solubility In Water Limited solubility (predicted)
    Density Estimated value
    Flash Point Estimated value
    Pka Estimated value
    Logp Estimated value

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    General Information
    Where to Buy 3,5-Dimethyl-2-Hydroxymethyl-4-Methoxypyridine in China?
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    Frequently Asked Questions

    As a leading 3,5-Dimethyl-2-Hydroxymethyl-4-Methoxypyridine 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-dimethyl-2-hydroxymethyl-4-methoxypyridine?
    3,5-Dimethyl-2-methoxy-4-methoxybenzaldehyde is an important organic compound with a wide range of uses in the field of organic synthesis. Its main uses are as follows:
    First, it plays a key role in drug synthesis. It can be used as a key intermediate to prepare a variety of drugs with specific biological activities. In the synthesis process of some drugs with antibacterial, anti-inflammatory, and anti-tumor effects, 3,5-dimethyl-2-methoxy-4-methoxybenzaldehyde can use a series of organic reactions to build the core skeleton of drug molecules or introduce key functional groups, thereby endowing the drug with specific pharmacological activities.
    Second, it also has outstanding performance in the field of fragrance synthesis. Due to its unique molecular structure, compounds with special aroma can be derived. Fragrance masters can use it as a starting material, chemically modify and prepare to create unique fragrances, which are used in perfumes, cosmetics, food additives and other industries to add the aroma charm of products.
    Third, it has emerged in the field of materials science. It can be used as an important raw material for the synthesis of functional materials. By polymerization or modification with other compounds, materials with specific optical, electrical or thermal properties can be prepared, showing potential application value in optoelectronic materials, polymer materials and other fields.
    Fourth, it provides an important tool for organic chemistry research. Scientists use it as a substrate to explore various reaction mechanisms, and by studying the chemical reactions it participates in, they can deeply understand the laws and characteristics of organic reactions, providing theoretical support and practical experience for the development of organic synthesis methodologies.
    What are the synthesis methods of 3,5-dimethyl-2-hydroxymethyl-4-methoxypyridine?
    To prepare 3% 2C5-dimethyl-2-methoxy-4-methoxybenzaldehyde, there are many methods, each with its advantages and disadvantages. The following are a few kinds.
    First, phenolic compounds are used as starting materials and are obtained by a series of reactions such as methoxylation and methylation. First, the phenolic hydroxyl group is reacted with reagents such as halomethane or dimethyl sulfate under basic conditions to introduce methoxy group, and then methyl group is introduced at the corresponding position under the action of a specific catalyst. Finally, the specific group is converted into an aldehyde group by oxidation and other steps. The raw materials in this way are often easy to obtain, but the reaction steps are complicated, and the reaction conditions need to be carefully adjusted to ensure the selectivity and yield of each step.
    Second, aromatic aldehyde derivatives are used as the starting materials and are achieved through selective methoxylation and methylation modification. First select aromatic aldodes with suitable substituents, use specific methoxylation reagents, introduce methoxy groups at the desired positions according to the reactivity and localization rules, and then carry out methylation operations. This method can simplify some steps and improve product selectivity by leveraging the localization effect of aldehyde groups in the starting materials, but the purity and source of the starting materials are quite high, and some reagents are expensive.
    Third, the coupling reaction strategy catalyzed by transition metals is used. Using halogen-containing aromatic compounds as substrates, methoxylating reagents and methylating reagents, and catalyzed by transition metal catalysts such as palladium and copper, methoxy groups and methyl groups are introduced, and then the basic skeleton of the target molecule is constructed, and then the aldehyde group is modified. The reaction conditions of this method are relatively mild, the atomic economy is good, and complex aromatic structures can be efficiently constructed. However, transition metal catalysts are expensive, and the post-reaction treatment requires fine operation to remove residual metal impurities.
    What are the physicochemical properties of 3,5-dimethyl-2-hydroxymethyl-4-methoxypyridine?
    3,5-Dimethyl-2-isopropyl-4-methoxybenzene is an organic compound with unique physical and chemical properties. Its physical properties are as follows: It is mostly liquid or solid at room temperature, and the melting and boiling points are different due to differences in intermolecular forces. The molecular structure causes its relative density to be different from that of water, or lighter than that of water floating on the water surface, or heavier than that of water sinking on the bottom. The compound is insoluble in water because it is an organic molecule with small polarity, and it is difficult to form effective interactions with water molecules; but it is soluble in organic solvents, such as ethanol, ether, etc., and follows the principle of similar compatibility. Organic solvents are similar to the structure and polarity of the compound. In terms of chemical properties, the benzene ring imparts its aromaticity and can undergo electrophilic substitution reactions, such as halogenation reactions. Under suitable catalysts, halogen atoms can replace hydrogen atoms on the benzene ring; in nitration reactions, nitro groups replace hydrogen atoms; in sulfonation reactions, sulfonic acid groups enter the benzene ring. Methoxy groups are the power supply subgroups, which can affect the electron cloud density distribution of the benzene ring, so that the electron cloud density of the adjacent and para-sites of the benzene ring increases, and electrophilic substitution reactions are more likely to occur in the adjacent and para-sites. Alkyl side chains can undergo oxidation reactions. For example, under specific conditions, isopropyl groups and methyl groups can be oxidized to corresponding oxygen-containing functional groups. These physical and chemical properties are of great significance in the fields of organic synthesis and medicinal chemistry, and can be used to prepare various organic compounds
    What is the price range of 3,5-dimethyl-2-hydroxymethyl-4-methoxypyridine in the market?
    Wen Jun inquired about the market price of 3% 2C5-dimethyl-2-methoxy-4-methoxybenzaldehyde, which is a fine chemical industry. Its price often varies depending on quality, quantity, current situation, and supply and demand.
    If it is of ordinary quality, if you buy a small amount, the price per gram may be in the range of tens to hundreds of yuan. However, if it is a high-purity boutique used in high-end scientific research and pharmaceuticals, the price will be high, or hundreds of yuan per gram, or even higher.
    If the purchase quantity is quite large, in terms of kilograms, the price per gram may drop significantly, or drop to tens of yuan per gram due to the benefits of wholesale. < Br >
    And the supply and demand of the market are also the main reasons for the price. If there are many applicants and few suppliers, the price will rise; if the supply exceeds the demand, the price will decline. The situation is different, and the price of raw materials, production costs, and transportation costs all change, causing their prices to fluctuate.
    In order to determine the price, it is advisable to consult the chemical raw material supplier and specify the required quality and quantity in detail before the exact number can be obtained.
    What are the storage conditions for 3,5-dimethyl-2-hydroxymethyl-4-methoxypyridine?
    The storage conditions of 3% 2C5-dimethyl-2-fluoromethyl-4-methoxybenzene need to be carefully considered for the preservation of these delicate things.
    These substances are fragile and easy to be disturbed by various external factors. The first to bear the brunt is the control of temperature. It should be placed in a cool place, and must not be exposed to the hot sun or in a hot place. Due to high temperature, it is easy to cause changes in its properties, or cause unpredictable changes. The ideal temperature is between 2 and 8 degrees Celsius, which is like the mild climate at the turn of spring and autumn, which can protect its stability.
    Furthermore, humidity is also the key. In a humid environment, the water vapor is dense, which makes it easy for the substance to absorb moisture, causing its purity to be damaged, or even breeding impurities. Therefore, the storage place must be dry, and a desiccant can be placed on the side to absorb excess moisture and keep it dry and clean.
    Light is also an element that cannot be ignored. Light, although it has the appearance of light, is too strong, especially ultraviolet light, which has powerful energy and can stimulate chemical reactions and damage the structure of the substance. Therefore, it needs to be hidden in a dark container, or placed in a dark room, free from light disturbance.
    And it should be separated from oxidizing and reducing substances. Due to the chemical nature or activity of the substance, it is easy to react with them and cause quality deterioration.
    The storage place also needs to be well ventilated. If the turbid gas gathers, it may cause poor local environment and affect the stability of the substance. The circulating air can carry away bad gas and keep the environment fresh. In this way, it is necessary to properly store and nourish 3% 2C5-dimethyl-2-fluoromethyl-4-methoxybenzene to maintain its inherent properties for a long time for future needs.