5 8 Difluoro 1 2 3 4 Tetrahydroisoquinoline Hydrochloride
quinoline thiophene imidazole thiazole

5,8-Difluoro-1,2,3,4-Tetrahydroisoquinoline Hydrochloride

Taiy Chemical

    Specifications

    HS Code

    551389

    Chemical Formula C9H9F2N·HCl
    Molecular Weight 205.63
    Appearance Typically a white to off - white solid
    Physical State Solid at room temperature
    Solubility Soluble in polar solvents like water and alcohols to some extent
    Melting Point Data may vary, needs specific experimental determination
    Purity Can be obtained in high purity grades, e.g., 95%+ in commercial products
    Stability Should be stored in a cool, dry place away from light and moisture to maintain stability
    Hazard Class May cause skin, eye and respiratory irritation; handle with appropriate safety measures

    As an accredited 5,8-Difluoro-1,2,3,4-Tetrahydroisoquinoline Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Competitive 5,8-Difluoro-1,2,3,4-Tetrahydroisoquinoline Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.

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    General Information
    Where to Buy 5,8-Difluoro-1,2,3,4-Tetrahydroisoquinoline Hydrochloride in China?
    As a trusted 5,8-Difluoro-1,2,3,4-Tetrahydroisoquinoline Hydrochloride manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading 5,8-Difluoro-1,2,3,4-Tetrahydroisoquinoline Hydrochloride 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 chemical properties of 5,8-difluoro-1,2,3,4-tetrahydroisoquinoline hydrochloride?
    5,8-Diene-1,2,3,4-tetrahydroisobenzofuranic anhydride is one of the organic compounds. Its chemical properties are quite unique and have the generality of acid anhydride.
    In this compound, the acid anhydride group is very active and can react with alcohols to form esters and carboxylic acids. When exposed to water, it is also easy to hydrolyze and convert into corresponding carboxylic acids. This hydrolysis reaction can proceed steadily under moderate conditions.
    And because of its diene-containing structure, it can participate in the Diels-Alder reaction. When suitable dienes and dienophiles coexist, new carbon-carbon bonds can be formed through this reaction to form complex cyclic compounds. This reaction is widely used in the field of organic synthesis.
    In addition, the conjugated double bond structure of 5,8-diene-1,2,3,4-tetrahydroisobenzofuranic anhydride shows certain optical properties under specific conditions. Its electron cloud distribution and conjugate system affect its absorption and emission of light. Chemists can adjust its optical properties by adjusting reaction conditions and modifying surrounding groups.
    Due to its structure and properties, 5,8-diene-1,2,3,4-tetrahydroisobenzofuranic anhydride has potential application value in many fields such as organic synthesis, materials science and medicinal chemistry. It can be used as a synthetic intermediate to prepare various compounds with special structures and properties.
    What are the main uses of 5,8-difluoro-1,2,3,4-tetrahydroisoquinoline hydrochloride?
    5,2,8-Diene-1,2,3,4-tetraaminoisopentene-photoflavin anhydride, which has important uses in many fields.
    In the field of medicine, its unique chemical structure shows potential biological activity, or can be used to create new drugs. After careful study, doctors have found that it has significant effects on specific disease-related targets, and it is expected to develop a good drug for difficult diseases and bring hope for recovery to patients.
    In the field of materials science, this compound may become a key raw material for the preparation of special functional materials. After repeated trials, craftsmen can use their characteristics to prepare materials with unique optical and electrical properties, such as high-sensitivity optical sensor materials, which can be used to accurately detect specific substances in the environment, and are of great significance in environmental monitoring, biological detection, etc.; or prepare special conductive materials, which can be used in advanced electronic devices to improve device performance.
    In the field of organic synthesis, 5,2,8-diene-1,2,3,4-tetraaminoisopentene photoflavin anhydride is like a delicate "key", which is an important intermediate for the construction of complex organic molecules. This allows us to design and synthesize organic compounds with novel structures and unique functions, opening up new paths for the development of organic chemistry, driving the field forward, and generating more innovative research results.
    What is the synthesis method of 5,8-difluoro-1,2,3,4-tetrahydroisoquinoline hydrochloride?
    To prepare 5% 2C8-diene-1% 2C2% 2C3% 2C4-tetraaminoisosquare photocysteine anhydride, the following method can be used.
    First take an appropriate starting material, which needs to contain a group capable of deriving the target structure. Usually start with unsaturated hydrocarbons or nitrogen-containing compounds with specific substituents. After ingenious reaction design, the unsaturated bond and the nitrogen-containing part gradually build the skeleton of the target molecule.
    One method can first introduce the amino group at a suitable position through nucleophilic substitution reaction. Select a halogenated hydrocarbon or sulfonate with suitable activity and react with ammonia or amine compounds under appropriate conditions. The conditions of the reaction are crucial, and the temperature, pH and reaction time need to be precisely regulated. Generally speaking, mild alkaline environments, such as aqueous solutions of potassium carbonate or sodium carbonate, can react at moderate temperatures (such as 50-80 degrees Celsius) to enable nucleophilic substitution reactions to proceed smoothly.
    When unsaturated bonds are formed, the elimination reaction is often achieved. Alcohols or halogenated hydrocarbons can be used to remove small molecules (such as water or hydrogen halide) under basic reagents and appropriate heating conditions to form carbon-carbon double bonds. Alcoholic solutions of sodium hydroxide can be selected for basic reagents, and heated to a reflux state to promote the elimination reaction to occur and construct a 5% 2C8-diene structure.
    During the synthesis process, the reaction process needs to be closely monitored. Thin-layer chromatography (TLC) can be used to observe the consumption of raw materials and the formation of products. According to the location and color changes of the spots on the TLC plate, determine whether the reaction is complete. When the reaction reaches the desired stage, it needs to go through the separation and purification step.
    The commonly used separation method is column chromatography. Silica gel is used as the stationary phase, and a suitable eluent, such as a mixed solvent of petroleum ether and ethyl acetate, is selected to achieve high-efficiency separation according to the difference in the polarity of the product and impurities. Finally, the product was further purified by recrystallization and other means to obtain pure 5% 2C8-diene-1% 2C2% 2C3% 2C4-tetraaminoisosquare cysteine anhydride. The whole synthesis process requires fine operation, paying attention to the condition control and product monitoring at each step, in order to successfully achieve the preparation of the target product.
    What is the price range of 5,8-difluoro-1,2,3,4-tetrahydroisoquinoline hydrochloride in the market?
    What is the market price of 5% 2C8-diene-1% 2C2% 2C3% 2C4-tetraaminoisoprene photosuccinate amber?
    In Guanfu City, the price of various materials is often different due to changes in time, place, quality and supply and demand. This 5% 2C8-diene-1% 2C2% 2C3% 2C4-tetraaminoisoprene photosuccinate amber is an unusually easy product. Its preparation may require exquisite methods, and the raw materials used may also be rare.
    If in the prosperous city of Kyoto, there are many businesses and many traders, when supply and demand, the price may be slightly higher. If the quality is high, the price per catty may reach tens of gold; if the quality is slightly inferior, it will also cost more than ten gold.
    And in remote cities, the transportation is inconvenient, and merchants are rare. This thing may be hard to find. Even if it is there, its price will be high, because the transshipment is difficult and the cost is doubled.
    Moreover, in times of abundance, the material resources are rich, and all workers are prosperous. These materials may be slightly increased due to the production, and the price may drop; if it is a famine, everything is difficult, the material resources are scarce, and the price will rise, which is not reasonable.
    As for the exact number, it is difficult to determine it quickly. The situation in the market is fickle, and you can only know the current price if you are close to the market and consult all merchants.
    What are the storage conditions for 5,8-difluoro-1,2,3,4-tetrahydroisoquinoline hydrochloride?
    5,8-Diene-1,2,3,4-tetraaminoisosquaric acid dicamide is a rather special chemical substance. Its storage conditions are crucial to the stability and effectiveness of this substance.
    According to the concept of "Tiangong Kaiwu", everything needs to be properly placed to maintain its properties. 5,8-diene-1,2,3,4-tetraaminoisquaric acid dicamide should be stored in a cool and dry place. Because the temperature is too high, or the chemical reaction of this substance occurs, its structure is damaged, and its original characteristics are lost. And humid environment is not advisable, moisture or interaction with the substance can cause adverse reactions such as hydrolysis.
    Furthermore, this substance should be placed in a dark place. Light can be used as an energy source to induce luminescent chemical reactions, which affect the chemical structure of 5,8-diene-1,2,3,4-tetraaminoisosquaric acid dicamide. Therefore, it needs to be stored in opaque containers, such as brown glass bottles, which can effectively block light and reduce the probability of photochemical reactions.
    In addition, the storage place should be kept away from fire sources and oxidants. 5,8-Diene-1,2,3,4-tetraaminoisosquaric acid dicamide may be flammable to a certain extent, and it is easy to cause fire when exposed to fire sources; and the contact of oxidants with it, or triggering a violent oxidation reaction, not only endangers the preservation of the substance itself, but also may lead to safety accidents.
    In short, in order to properly store 5,8-diene-1,2,3,4-tetraaminoisquaric acid dicamide, it must be cool, dry, protected from light, and away from fire sources and oxidants, so as to maintain the stability of its chemical properties for subsequent use.