6 7 Dihydroxy 3 4 Dihydroisoquinoline
quinoline thiophene imidazole thiazole

6,7-Dihydroxy-3,4-Dihydroisoquinoline

Taiy Chemical

    Specifications

    HS Code

    567661

    Chemical Formula C9H9NO2
    Molar Mass 163.173 g/mol
    Appearance Solid (predicted)
    Solubility In Water Low solubility (predicted)
    Solubility In Organic Solvents Soluble in some organic solvents (predicted)
    Stability Stable under normal conditions (predicted)
    Potential Reactivity Reactive towards certain reagents (predicted)

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    General Information
    Where to Buy 6,7-Dihydroxy-3,4-Dihydroisoquinoline in China?
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    Frequently Asked Questions

    As a leading 6,7-Dihydroxy-3,4-Dihydroisoquinoline 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 main use of 6,7-dihydroxy-3,4-dihydroisoquinoline?
    6,7-diamino-3,4-dihydroxyisoflavone, this is a kind of very important organic compounds, which has key uses in many fields.
    In the field of medicine, it has shown quite excellent biological activity. Many studies have shown that the substance has certain antioxidant effects. It can effectively scavenge free radicals in the body, slow down the process of oxidative damage to cells, and may help prevent diseases such as cardiovascular diseases and neurodegenerative diseases caused by oxidative stress. At the same time, it has also attracted much attention in anti-tumor. Some experiments suggest that 6,7-diamino-3,4-dihydroxy isoflavones may inhibit the proliferation of tumor cells, or induce tumor cell apoptosis by affecting the signaling pathway of tumor cells, providing new ideas and directions for the development of anti-tumor drugs.
    In the field of agriculture, it also has unique applications. Because of its structural characteristics, it may have a positive impact on plant growth and development. For example, it can regulate the hormone balance of plants, promote the growth and development of plant roots, enhance the resistance of plants to environmental stress, such as improving the ability of plants to resist drought, cold and pests, thereby improving the yield and quality of crops.
    In addition, in the field of materials science, 6,7-diamino-3,4-dihydroxyisoflavone may be used as a key raw material for the construction of new functional materials due to its special molecular structure. Through reasonable molecular design and modification, materials with specific optical, electrical or magnetic properties may be prepared, which have potential application value in optoelectronic devices, sensors and other fields.
    In conclusion, 6,7-diamino-3,4-dihydroxyisoflavone, with its unique structure and diverse properties, has played an important role in many important fields such as medicine, agriculture and materials science. In-depth research and development of it is expected to bring innovative breakthroughs and development in many fields.
    What are the physical properties of 6,7-dihydroxy-3,4-dihydroisoquinoline
    6,7-Diamino-3,4-dihydroxyquinoxaline dihydrochloride is a special compound with unique physical properties.
    Looking at its morphology, it is usually solid, mostly crystalline, and the crystals are fine and regular, just like natural delicate things. Its color is usually white to light yellow. When it is pure, it is white like frost, but if there are a little impurities or affected by external factors, it is slightly yellowish, just like a thin cloud in the early morning light.
    When it comes to solubility, this compound exhibits a certain solubility in water. Water is the source of life, and the dissolution properties of many substances in it are crucial. 6,7-diamino-3,4-dihydroxyquinoxaline dihydrochloride can be moderately dissolved in water to form a uniform dispersion system, but its solubility is not infinite and is restricted by factors such as temperature and concentration. In organic solvents, its solubility varies. In some polar organic solvents, the solubility may be slightly higher, while in non-polar organic solvents, the solubility is relatively weak.
    Let's talk about the melting point, which is one of the important physical properties of matter. 6,7-diamino-3,4-dihydroxyquinoxaline dihydrochloride has a specific melting point. When the temperature rises to a certain value, its solid state begins to transform into a liquid state. This transformation process, like the melting of ice and snow, is the embodiment of the change of the internal structure of the substance and the force between molecules. By accurately measuring the melting point, the purity and other properties of the compound can be effectively judged.
    Its stability cannot be ignored. Under normal temperature and pressure without special external interference, 6,7-diamino-3,4-dihydroxyquinoxaline dihydrochloride can maintain a relatively stable state. However, in the event of extreme environments such as high temperature, strong acid, and strong alkali, its structure may change, just as a building encounters strong earthquakes, challenging its stability, which in turn affects its physical and chemical properties.
    What are the chemical properties of 6,7-dihydroxy-3,4-dihydroisoquinoline
    6,7-diamino-3,4-dihydroxyisoflavone, this is a rather unique organic compound, its chemical properties are particularly rich.
    It is weakly acidic. Because of the hydroxyl groups in the molecule, protons can be dissociated under appropriate conditions, showing acidic characteristics. Although this acid is not a strong acid, it can neutralize with bases in a specific chemical reaction environment to generate corresponding salts.
    Furthermore, it is nucleophilic. The amino and hydroxyl groups in the molecule are rich in lone pair electrons, so they have nucleophilic ability. In nucleophilic substitution reactions, lone electrons of amino or hydroxyl groups can attack electrophilic reagents, resulting in the formation of new chemical bonds, such as nucleophilic substitution with halogenated hydrocarbons to form novel nitrogenous or oxygen-containing derivatives.
    The conjugated system also gives it unique chemical activity. The conjugated structure of 6,7-diamino-3,4-dihydroxyisoflavone allows electrons to delocalize throughout the conjugated system, enhancing the stability of the molecule. However, this conjugated system also makes the molecule more susceptible to attack by electrophilic reagents, triggering electrophilic substitution reactions. In electrophilic substitution, electrophilic reagents will attack the higher electron cloud density of the conjugated system and generate various substitution products.
    In addition, it can also participate in hydrogen bonding. Both amino and hydroxyl groups in the molecule can be used as hydrogen bond donors, and their carbonyl groups can also be used as hydrogen bond receptors. Through hydrogen bonding, the compound can interact with other molecules containing hydrogen bond receptors or donors, which plays a key role in the aggregation state in solution, mutual recognition with biological macromolecules, and the formation of crystal structures.
    And the compound has certain coordination ability to some metal ions. The amino and hydroxyl oxygen atoms in the molecule can be used as ligands to form coordination bonds with metal ions to form metal complexes. This coordination may have a significant impact on its physicochemical properties and biological activities.
    What are the synthesis methods of 6,7-dihydroxy-3,4-dihydroisoquinoline
    The synthesis method of 6,7-difluoro-3,4-dicyanoisosquaric acid is a key research in the field of chemical synthesis. Its synthesis paths are diverse, each has its own advantages and disadvantages, and needs to be carefully selected according to the actual situation.
    First, it can be initiated by a specific halogenation reaction. Using aromatic hydrocarbons containing appropriate substituents as raw materials, fluorine atoms are introduced precisely through halogenation reactions to construct fluorine-containing intermediates. This step requires careful control of the reaction conditions, such as temperature, catalyst type and dosage, etc. Due to the selectivity and yield of halogenation reactions, this condition is closely related. Then, through a series of reactions such as nucleophilic substitution, cyanide groups are introduced to gradually build the target molecular structure. The advantage of this path is that the raw materials are relatively easy to obtain, and the logic of the steps is clear; however, the selective regulation of the halogenation reaction is quite difficult, which is prone to side reactions, resulting in product purity and yield being affected.
    Second, the cyclization reaction strategy can be adopted. Select chain compounds with specific functional groups, and through carefully designed cyclization reactions, one step builds the core skeleton of isosquaric acid, and at the same time ingeniously introduce fluorine and cyanyl groups. The key to this path lies in the optimization of the conditions of the cyclization reaction, involving factors such as reaction solvent, reaction time and temperature. If the conditions are suitable, the target product can be efficiently synthesized, the steps can be reduced, and the atomic economy can be improved. However, the structural design requirements of the starting materials are extremely high, and the positions and activities of each functional group in the molecule need to be carefully planned to ensure that the cyclization reaction can occur as expected.
    Third, there are also simple compounds containing fluorine and cyanide groups as starting materials, and the target synthesis is achieved through functional group conversion and condensation reactions. The advantage of this approach is that it can take advantage of the characteristics of existing compounds to simplify some synthesis steps. However, it is necessary to pay attention to the selectivity of functional group conversion and the matching of condensation reaction conditions to avoid unnecessary by-products.
    All these synthesis methods require chemists to use their exquisite skills and in-depth understanding, comprehensively consider factors such as raw material cost, feasibility of reaction conditions, product yield and purity, and through repeated experiments and optimization, to find the most suitable synthesis strategy. To achieve the efficient and high-purity synthesis of 6,7-difluoro-3,4-dicyanoisosquaric acid.
    What is the price range of 6,7-dihydroxy-3,4-dihydroisoquinoline in the market?
    In today's market, the price of 6,7-dimethyl-3,4-dihydroxyisoflavone varies depending on the category, quality, supply and demand.
    If it is an ordinary product, its price may be between tens and hundreds of dollars per gram. Such a price is mostly for daily business use, the quality is moderate, and it can meet general needs.
    However, if it is a refined top product, with excellent selection of materials, exquisite craftsmanship, and extremely high purity, its price is much more than this. The price per gram may reach thousands or even thousands of dollars. These top products are mostly needed by high-seeking businesses and are used for fine research and precious systems.
    There are also changes due to the supply and demand of the city. If there are many people who ask for it, but there are few people who supply it, the price will inevitably increase; on the contrary, if the supply exceeds the demand, the price may also drop.
    And the price varies in different places. The prosperous capital is Dayi, where business is frequent, the price may be slightly higher because of it; in remote places, the circulation is inconvenient, and the price may vary.
    Therefore, if you want to know the exact price, you need to carefully check the city conditions and visit merchants before you can get it.