4 5 6 Dimethoxy 1 Indanone 2 Methyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

4-[(5,6-dimethoxy-1-indanone)-2-methyl] pyridine

    Specifications

    HS Code

    947199

    Chemical Formula C17H19NO3
    Molecular Weight 285.34
    Appearance Typically a solid (description may vary based on purity and conditions)
    Physical State At Room Temperature Solid
    Solubility In Water Poorly soluble (due to non - polar nature of most of the molecule)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Pka No common value found, likely related to the basicity of the pyridine nitrogen
    Logp Estimated to be relatively high due to non - polar aromatic and aliphatic parts

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    General Information
    Where to Buy 4-[(5,6-dimethoxy-1-indanone)-2-methyl] pyridine in China?
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    Frequently Asked Questions

    As a leading 4-[(5,6-dimethoxy-1-indanone)-2-methyl] pyridine 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- [ (5,6-dimethoxy-1-indanone) -2-methyl] pyridine?
    This is a compound of 4- [ (5,6-diacetyl-1-naphthmanone) - 2-methyl]. Its physical properties are as follows:
    Looking at its appearance, it often takes the form of a white to off-white crystalline powder. Under sunlight, it resembles a delicate frost powder and shines.
    When it comes to the melting point, it is usually in a specific temperature range, roughly within the [specific melting point range]. This property is like its unique "temperature code". When the external temperature rises to this range, the compound will undergo a phase change. < Br >
    In terms of solubility, it shows a certain solubility in organic solvents, such as ethanol and acetone. In ethanol, it is like snowflakes fused into spring water, gradually dispersing and dissolving to form a uniform solution; however, in water, its solubility is poor, just like the ping on the water, and it is difficult to blend. This is due to the difference between its molecular structure and the force between water molecules.
    Density is also one of its important physical properties, with a specific value, like giving it a unique "weight mark", reflecting the compactness of its internal microstructure.
    In addition, the stability of this compound cannot be ignored. In the conventional temperature and humidity environment, it can maintain relative stability, like a calm person, and will not be shaken by slight changes in the outside world; but in the case of extreme chemical environments such as strong acids and alkalis, or conditions such as high temperature and strong light, its structure may change, just like a delicate flower in the face of wind and rain, it is difficult to maintain its original form.
    All the above physical properties are of vital significance in many fields such as chemical synthesis and drug research and development, like the key to opening the door to scientific research, helping researchers to further explore its potential application value.
    What are the chemical synthesis methods of 4- [ (5,6-dimethoxy-1-indanone) -2-methyl] pyridine?
    To obtain 4- [ (5,6-diacetyl-1-naphthalmonone) - 2-acetyl], the chemical synthesis method has various paths, which are described in detail below.
    First, it can be initiated by acylation of naphthalene. With naphthalene as the base, the first reaction with acetic anhydride under the catalysis of an appropriate catalyst, such as anhydrous aluminum trichloride, occurs Fu-gram acylation, and the acetyl group is introduced into the naphthalene ring. Due to the difference between the α and β positions of the naphthalene ring, the control of the reaction conditions is extremely critical. Under suitable conditions, the acetyl group can be mainly introduced into the α position to obtain 1-acetylnaphthalene. Subsequently, 1-acetyl naphthalene is further acylated with another molecule of acetic anhydride under similar conditions, and a second acetyl group is introduced. After a multi-step reaction, the reaction conditions are finely regulated to generate 5,6-diacetyl-1-naphthalmanone. Finally, this product is reacted with an acetylation reagent, such as acetyl chloride, in the presence of a base, and an acetyl group is introduced at the 2 position to obtain the target product.
    Second, other aromatic derivatives can also be started. Select a suitable aromatic hydrocarbon with a functional group that can be converted into an acetyl group, and construct the target structure through a series of functional group conversion and cyclization reactions. For example, an aromatic derivative containing an alkenyl group and a carbonyl group is first cyclized within the molecule under the action of a specific catalyst to form the basic skeleton of naphthenone, and then the acetyl group is gradually introduced at a suitable position through oxidation, acylation and other steps. For example, by using the carbon-carbon bond formation reaction catalyzed by transition metals, the acetyl fragment is cleverly connected to the naphthenone skeleton, and the required 4- [ (5,6-diacetyl-1-naphthenone) -2-acetyl] is obtained after a multi-step reaction.
    Furthermore, the method of biomimetic synthesis can also be considered. Mimicking the mechanism of synthesizing such compounds in vivo, using enzyme catalysis or biotransformation methods. Enzymes with specific activities, such as certain oxidases, acyltransferases, etc., are used to catalyze the conversion of simple substrates under mild reaction conditions. Starting from naturally occurring compounds with relatively simple structures, through the specific catalysis of enzymes, complex target molecular structures are gradually constructed to achieve the synthesis of 4- [ (5,6-diacetyl-1-naphthmanone) -2-acetyl]. This path has the advantages of mild reaction conditions and high selectivity.
    What are the main uses of 4- [ (5,6-dimethoxy-1-indanone) -2-methyl] pyridine?
    4 - [ (5,6 - diacetyl - 1 - naphthmanone) - 2 - methyl] The main use of this substance is related to many fields such as medicine and chemical industry.
    At the end of medicine, it may be a key intermediate for the synthesis of specific drugs. Because the structure has unique chemical activity and spatial configuration, it can be precisely spliced with other molecules through specific chemical reactions to construct complex compounds with specific pharmacological activities. For example, it can be used to develop targeted drugs for specific diseases. By precisely acting on specific targets of diseased cells, efficient treatment can be achieved, and it is expected to reduce damage to normal cells and improve drug efficacy and safety.
    In the chemical industry, it is also widely used. It can be used as an important raw material for the synthesis of high-performance materials. Due to the stable molecular structure and special electron cloud distribution, the synthesized materials may have excellent physical and chemical properties, such as hot topic stability, excellent mechanical properties, etc. It is suitable for the manufacture of high-end engineering plastics, special fibers, etc., to meet the strict requirements of materials in frontier fields such as aerospace and electronic technology. For example, in the manufacture of aerospace parts, the use of this synthesized material can reduce the weight of parts, while maintaining high strength and stability, and help improve the performance of aircraft.
    In addition, in the study of organic synthetic chemistry, it serves as a classical structural unit, providing a basis for organic chemists to explore novel reaction paths and synthesis strategies. By means of chemical modification and transformation, scholars have developed new organic synthesis methods and promoted the development of organic chemistry.
    What are the precautions for storing and transporting 4- [ (5,6-dimethoxy-1-indanone) -2-methyl] pyridine?
    If you want to make 4- [ (5,6-diethoxy-1-naphthalmonone) -2-ethyl], pay attention to everything during its storage and transportation.
    When storing, the first environment. It needs to be placed in a cool, dry and well-ventilated place. Because the substance may be sensitive to temperature and humidity, it is easy to deteriorate due to high temperature and humidity. If it is exposed to high temperature, the molecular activity will increase, or chemical reactions will be triggered to change the composition; humid environment may cause the substance to absorb moisture, which affects the purity.
    Furthermore, it should be stored separately from oxidants, acids, bases, etc. This substance is chemical or active, contact with the above substances, or react violently, causing fire, explosion and other risks. If the oxidant has strong oxidizing properties, mix with it, or cause an oxidation reaction, releasing a lot of heat.
    When transporting, the packaging must be solid. Choose suitable packaging materials to ensure that it is not damaged by vibration or collision during transportation. Otherwise, once it leaks, it will not only lose the material, but also endanger the transporter and the surrounding environment.
    The transportation tool needs to be clean and dry, and there are no impurities that react with the substance. And the transportation process should avoid high temperature and open flames. Summer transportation may require cooling measures; especially when passing through open flame areas such as gas stations.
    The escort personnel also need to be professional and familiar with the characteristics of the substance and emergency treatment methods. In case of emergencies, such as leakage, they can respond quickly and take effective measures to minimize harm.
    What are the market prospects for 4- [ (5,6-dimethoxy-1-indanone) -2-methyl] pyridine?
    Today, there is a product name 4- [ (5,6-diacetyl-1-naphthalmanone) -2-methyl], and its market prospects are as follows:
    This product has considerable applications in today's pharmaceutical industry and chemical industry. In medicine, because of its unique chemical structure or potential biological activity, it can be used as a key intermediate for the development of new drugs. Nowadays, pharmaceutical research and innovation seeks more new drugs with high efficiency and low toxicity. This product may be able to fit with specific targets in the body due to its special structure to achieve the purpose of treating diseases. Looking at the market, new drug R & D requests are eager, and the demand for high-quality intermediates is also rising. Therefore, if this product can be used to develop new drugs, once successful, the market prospect will be limitless.
    In the chemical industry, it can be used as a raw material for the synthesis of special materials. Today's material field pursues high-performance, multi-functional materials. The materials involved in the synthesis may have unique physical and chemical properties, such as high stability, excellent optical properties, etc., which can be applied to high-end fields such as electronics and optics. And these high-end fields are developing rapidly, and the demand for characteristic materials continues to rise, providing them with a broad market space.
    However, its market expansion also faces challenges. The synthesis process of this product may be complicated and costly. Complex processes lead to low production efficiency and high costs weaken market competitiveness. And similar alternatives may already exist in the market. If you want to stand out, you must find a delicate balance between quality and price. And regulatory policies require strict requirements for pharmaceutical and chemical products, and the road to compliance needs to be moved forward cautiously.
    In summary, the market situation of 4- [ (5,6-diacetyl-1-naphthenone) -2-methyl] has bright prospects and challenges. If you can break the technical and cost dilemma and follow the regulatory regulations, you will be able to occupy a place in the market.