1 3 2h 4h Isoquinolinedione 7 Methoxy 2 4 4 Trimethyl
quinoline thiophene imidazole thiazole

1,3(2H,4H)-isoquinolinedione, 7-methoxy-2,4,4-trimethyl-

Taiy Chemical

    Specifications

    HS Code

    868949

    Chemical Name 1,3(2H,4H)-isoquinolinedione, 7-methoxy-2,4,4-trimethyl-
    Molecular Formula C14H17NO3
    Molecular Weight 247.29
    Appearance Unknown
    Melting Point Unknown
    Boiling Point Unknown
    Solubility Unknown
    Density Unknown
    Flash Point Unknown
    Pka Unknown

    As an accredited 1,3(2H,4H)-isoquinolinedione, 7-methoxy-2,4,4-trimethyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    General Information
    Where to Buy 1,3(2H,4H)-isoquinolinedione, 7-methoxy-2,4,4-trimethyl- in China?
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    Frequently Asked Questions

    As a leading 1,3(2H,4H)-isoquinolinedione, 7-methoxy-2,4,4-trimethyl- supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of 1,3 (2H, 4H) -isoquinolinedione, 7-methoxy-2,4,4-trimethyl-
    This is an investigation into the chemical structure of 7-methoxy-2,4,4-trimethyl-1,3 (2H, 4H) -isoquinolinedione. According to this designation, according to the rules of organic chemistry, isoquinoline is the parent nucleus. In the isoquinoline structure, there is a carbonyl group attached to the carbon at positions 1 and 3, and this dicarbonyl group is related to 2H and 4H, respectively, or is a specific reaction check point or bonding state. The 7-position is connected with a methoxy group, that is, an -OCH group. And the 2,4,4-position is connected with a methyl group, that is, a -CH group.
    As a whole, the structure of this compound has a unique spatial configuration and chemical properties due to these substituents. The electron characteristics of methoxy groups may affect the distribution of the electron cloud of the parent nucleus, and the introduction of methyl groups will also change the properties of molecular polarity and steric hindrance.
    In this structure, the conjugated system of the parent nucleus of isoquinoline may endow it with specific optical and electronic properties. The presence of carbonyl groups may make it electrophilic and can participate in many organic reactions, such as nucleophilic addition. The synergistic effect of substituents at different positions shapes the unique chemical behavior of this compound, which may have specific applications in organic synthesis, medicinal chemistry and other fields.
    What are the physical properties of 1,3 (2H, 4H) -isoquinolinedione, 7-methoxy-2,4,4-trimethyl-
    7-Methoxy-2,4,4-trimethyl-1,3 (2H, 4H) -isoquinolinedione, which has the following physical properties:
    Its appearance or crystalline, white and pure is the top grade, like suet jade. Melting point or in a specific range, just like the process that needs to be precisely controlled by the heat, this is the key node of its thermal change, related to its morphological transformation. In terms of solubility, in some organic solvents, such as alcohols, it is as soluble as fish in water, but in water, it is as difficult to blend as oil and water. This property is like the difference between things.
    Its density is like a scale for measuring its internal compactness, with a specific value, similar to the density of human bones, giving it a unique texture. Its stability cannot be ignored. Under normal temperature, it is like a calm old man, which can maintain its own structure and properties for a long time; in case of extreme situations such as high temperature, strong acid and alkali, it will be in case of rough seas, and the structure or change will also change, and the properties will also change.
    In addition, its spectral characteristics are unique. In the infrared spectrum, each absorption peak is distributed like a star, corresponding to the vibration of a specific functional group, which is like a unique fingerprint, which becomes an important basis for identifying this substance. In mass spectrometry, the arrangement and combination of the ion peaks of the fragments are also like a code, waiting for the wise to interpret to clarify their molecular structure and composition. Such various physical properties are like a delicate picture, outlining the unique appearance of 7-methoxy-2,4,4-trimethyl-1,3 (2H, 4H) -isoquinolinodione.
    What are the common uses of 1,3 (2H, 4H) -isoquinolinedione, 7-methoxy-2,4,4-trimethyl-
    1% 2C3% 282H% 2C4H% 29 - isoquinolinedione%2C + 7 - methoxy - 2% 2C4% 2C4 - trimethyl - that is, 7 - methoxy - 2,4,4 - trimethyl - 1,3 (2H, 4H) - isoquinolinedione, this is an organic compound. However, there is no relevant record of this compound in ancient China, nor is there any description of its common use. Because it is the product of modern chemical synthesis, it is difficult to find in ancient books, medical techniques, and other records. Ancient chemical technology is far less than today, and it is not capable of synthesizing such complex organic compounds.
    The common use of this compound depends on modern chemical and scientific research. In modern times, it can be used as a key intermediate in the field of organic synthesis to prepare complex organic molecules with special structures and functions. In medicinal chemistry, the relationship between its structure and activity can be studied, and new drugs can be developed, which will contribute to the development of medicine. In the field of materials science, modification and modification may endow materials with unique properties, such as optical and electrical properties, and are used in fields such as luminescent materials and semiconductor materials. However, these are all uses discovered based on modern scientific cognition and technology, and cannot be found in ancient times.
    What are the preparation methods of 1,3 (2H, 4H) -isoquinolinedione, 7-methoxy-2,4,4-trimethyl-
    To prepare 7-methoxy-2,4,4-trimethyl-1,3 (2H, 4H) -isoquinolinedione, the method is as follows:
    Take an appropriate amount of starting material first, and after many fine steps, this product can be achieved. The starting material needs to be skillfully processed before entering the reaction process.
    The first step is to select a suitable organic compound, mix it in a specific ratio, and place it in a delicate reaction vessel. In the meantime, precise temperature and pressure are controlled to make a delicate chemical reaction take place between the materials. This reaction, such as the harmony of yin and yang between heaven and earth, blends the materials with each other, and gradually generates the prototype of the desired product.
    In the second step, after the first step of the reaction is slightly completed, a specific reagent is applied. This reagent is like a stroke of magic, guiding the reaction in the expected direction. In the meantime, closely monitor the progress of the reaction, such as observing changes in celestial phenomena. If there is a slight mistake, it may fall short.
    Furthermore, after the reaction is completed, it needs to go through the process of separation and purification. This process is like panning gold in sand, removing its impurities and leaving its essence. With exquisite separation technology, the product is precipitated from the reaction mixture and purified, so that the purity of the product is extremely high.
    The whole process requires exquisite skills, subtle conditions, step by step caution, and walking on thin ice to obtain this 7-methoxy-2,4,4-trimethyl-1,3 (2H, 4H) -isoquinolinodione. Each step contains the wonders of heaven and earth creation and the ingenuity of human control. Only when you are done can you achieve success.
    What are the safety precautions for 1,3 (2H, 4H) -isoquinolinedione, 7-methoxy-2,4,4-trimethyl-
    7-Methoxy-2,4,4-trimethyl-1,3 (2H, 4H) -isoquinolinedione, this is an organic compound. Regarding its safety precautions, it should be described in detail in the old saying:
    This compound has certain chemical activity, and it must be handled with caution. First and foremost, users should use suitable protective equipment, such as special clothes, gloves, and face masks, to prevent the compound from coming into contact with the body and skin, or accidentally entering the eyes, because it may cause skin discomfort, eye damage.
    Furthermore, the operation should be in a well-ventilated place. If in a secret room, the gas released by the compound may cause air pollution, endangering the user's breathing. If the gas is heavy, or makes people dizzy, nauseous, and even damages the lungs.
    When storing, it is also important to pay attention. It must be placed in a cool, dry place, away from fire and heat sources. This compound encounters fire or heat, or reacts violently, or even causes an explosion, endangering the safety of the surrounding area.
    In addition, the use of this compound must be based on precise methods and dosages. If the dosage is excessive, or the reaction is out of control, an accident will occur. And after use, the residue should also be properly disposed of, and it should not be discarded at will, so as to prevent pollution and soil and harm the environment.
    In short, handle 7-methoxy-2,4,4-trimethyl-1,3 (2H, 4H) -isoquinolinedione with care at every step to ensure safety.