4 Bromoisoquinoline Hydrobromide
quinoline thiophene imidazole thiazole

4-bromoisoquinoline hydrobromide

Taiy Chemical

    Specifications

    HS Code

    108441

    Chemical Formula C9H7Br2N
    Molecular Weight 274.97
    Appearance Solid
    Color Off - white to light yellow
    Melting Point 240 - 245 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane
    Purity Typically high - purity available, e.g., 98%+
    Odor Odorless or very faint odor
    Stability Stable under normal conditions, but avoid strong oxidizing agents

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    General Information
    Where to Buy 4-bromoisoquinoline hydrobromide in China?
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    Frequently Asked Questions

    As a leading 4-bromoisoquinoline hydrobromide 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 4-bromoisoquinoline hydrobromide?
    4-Bromoisoquinoline hydrobromide is an organic compound. It has unique chemical properties and can be discussed from the poly-end.
    Looking at its structure, 4-bromoisoquinoline partially contains nitrogen heterocycles, which makes it alkaline to a certain extent. Nitrogen atoms can be combined with protons to form a salt, that is, hydrobromide. The salt should have good solubility in polar solvents such as water. Due to its ionization structure, it can have strong interactions with water molecules. For example, the ion-dipole force makes the molecules uniformly dispersed in the solvent.
    On its reactivity, the bromine atom is the active check point. Nucleophilic substitution reaction can occur. In case of nucleophilic reagents, the halogen atom bromine can be replaced to form new organic compounds. If the nucleophilic reagents are alkoxides, amines, etc., ether or amine substitution products can be formed respectively. And due to the electron cloud distribution of the isoquinoline ring, the reactivity of the 4-position bromine atom is affected by the electron effect on the ring. The change of electron cloud density on the ring can change the difficulty of nucleophilic substitution reaction.
    And because of its nitrogen-containing heterocyclic ring, it can participate in various cyclization reactions. If it reacts with compounds with appropriate functional groups, through the cyclization process, a more complex polycyclic system can be formed. It has important uses in the field of organic synthesis and can be used to construct drug intermediates or functional materials 4-Bromoisoquinoline hydrobromide has many potential applications and research values in organic synthesis and related fields due to its structure and properties.
    What are the common uses of 4-bromoisoquinoline hydrobromide?
    4-Bromoisoquinoline hydrobromide, its common uses are as follows:
    In the field of medicinal chemistry, it is often used as an important intermediate in organic synthesis. Due to its unique structure, a series of chemical reactions can be used to construct the structural skeleton of compounds with specific pharmacological activities. For example, using 4-bromoisoquinoline hydrobromide as the starting material, through substitution reaction, different functional groups are introduced to synthesize new drug molecules with potential antibacterial, anti-tumor and other biological activities.
    In materials science, it also plays a certain role. Can participate in the preparation of organic materials with special photoelectric properties. With the help of the reactivity of its bromine atom, it can be condensed with other organic molecules containing specific functional groups to synthesize functional materials that can be used in organic Light Emitting Diode (OLED), solar cells and other devices, and improve the properties of charge transport and luminous efficiency of the materials.
    In organic synthetic chemistry, it is a key starting material for the construction of complex isoquinoline derivatives. Through palladium-catalyzed cross-coupling reaction, it can react with aryl boric acid and other reagents to realize arylation modification on the isoquinoline ring, thereby expanding the conjugation system of the molecule and laying the foundation for the synthesis of organic compounds with unique physical and chemical properties.
    What is the synthesis method of 4-bromoisoquinoline hydrobromide?
    The synthesis of 4-bromoisoquinoline hydrobromide is a key research point in the field of organic synthesis. The synthesis path can be initiated by isoquinoline and reached by bromination reaction.
    First, in an appropriate reaction vessel, put an appropriate amount of isoquinoline and dissolve it in a specific organic solvent, such as dichloromethane. This solvent has good solubility and chemical stability, which is conducive to the smooth progress of the reaction. Then, in a low temperature environment, such as ice bath conditions, slowly add brominating reagents dropwise, usually bromine or N-bromosuccinimide (NBS). The amount of brominating reagent needs to be precisely controlled according to the reaction stoichiometry to prevent excessive bromination. < Br >
    When the brominating reagent is added dropwise, gradually heat up to room temperature or moderate temperature, so that the reaction can be fully carried out. During this period, the reaction progress is often monitored by means of thin layer chromatography (TLC). When the raw material point disappears and the product point appears significantly, the reaction is almost complete.
    After the reaction is completed, pour the reaction mixture into an appropriate amount of ice water to quench the unreacted reagent. Subsequently, extract the product with a suitable organic solvent, such as ether. The extract is dried with anhydrous sodium sulfate to remove water. Finally, the organic solvent is removed by vacuum distillation to obtain a crude product.
    The crude product can be refined by column chromatography or recrystallization. In column chromatography, appropriate silica gel and eluent are selected to achieve effective separation of the product and impurities; recrystallization is based on the solubility difference of the product in different solvents, and a suitable solvent is selected, such as ethanol-water mixed solvent. After recrystallization, pure 4-bromoisoquinoline can be obtained.
    To obtain 4-bromoisoquinoline hydrobromide, the purified 4-bromoisoquinoline can be dissolved into an appropriate amount of hydrobromic acid solution, stirred evenly, so that the two can fully react. After the reaction is completed, the solvent is evaporated to obtain the white crystalline product of 4-bromoisoquinoline hydrobromide. The whole synthesis process requires strict control of reaction conditions and precise operation to obtain high-purity target products.
    What are the precautions for 4-bromoisoquinoline hydrobromide in storage and transportation?
    For 4-bromoisoquinoline hydrobromide, there are several ends that need to be paid attention to during storage and transportation.
    First storage environment. When placed in a cool, dry and well-ventilated place. This medicine is easy to decompose and deteriorate when heated. If it is exposed to high temperature, its chemical structure may be damaged, resulting in drug efficacy loss. Therefore, the warehouse temperature should be controlled within an appropriate range, and it should not be overheated. And humid gas is also a big taboo, because it may lead to drug deliquescence, which will cause chemical reactions and damage its quality.
    Times and packaging. It must be stored in a sealed container to prevent it from contacting with air and moisture. High-quality packaging can ensure that the medicine can be stored for a long time without changing. After taking it, it should also be sealed immediately and not exposed to the outside.
    As for transportation, shock resistance and anti-collision are extremely important. This medicine is a chemical substance, and the structure may be fragile, causing bumps and vibrations during transportation, or causing package damage and drug leakage. Therefore, when handling, it is advisable to handle it with care and fix it properly to avoid damage.
    Furthermore, transportation and storage must be kept away from fire sources, heat sources and strong oxidants. 4-Bromoisoquinoline hydrobromide may react violently when encountering such substances, causing fire, explosion and other risks, endangering personnel and environmental safety.
    It also needs to be operated in accordance with relevant regulations and standards. When storing and transporting such chemicals, it is necessary to comply with national and local safety regulations, and make labels and records to clarify their characteristics, hazards, and disposal methods. In case of emergencies, it can also be handled calmly.
    What is the market price of 4-bromoisoquinoline hydrobromide?
    Today there are 4-bromoisoquinoline hydrobromide, but the price in the market is difficult to say for sure. The price of 4-bromoisoquinoline hydrobromide varies due to many reasons, such as the distance of the source, the difficulty of preparation, and the amount of purchase, all of which are related to it.
    In the past, the price of chemical materials often moved due to world events. If there are many producers, the supply will exceed the demand, and the price will drop; if the raw materials are rare and difficult to produce, or there are many applicants, the supply will exceed the demand, and the price will rise.
    4-bromoisoquinoline hydrobromide is used in various chemical industries, such as the genus of pharmaceutical synthesis. In the market, if it comes from a nearby place, and it is convenient to make, the raw materials are also easy to produce, and the supply is sufficient but the demand is not burning, the price is flat. However, if it needs to be done far away, and the production is complicated, the raw materials are rare, and there are many people seeking, the price will be high.
    With common sense, the inter-market price may be between a few yuan and a few dozen yuan per gram, but this is only a rough estimate. The actual price must be consulted in the cities, or the price of recent transactions can be obtained. The market is impermanent, and the price changes at any time. Therefore, if you want to know the details, you must refer to the real-time situation.