3 Bromo 2 Hydroxypyridine
pyridine pyrrole pyrazine piperidine piperazine

3-Bromo-2-hydroxypyridine

    Specifications

    HS Code

    286093

    Chemical Formula C5H4BrNO
    Molar Mass 172.00 g/mol
    Appearance Solid
    Color Off - white to light yellow
    Melting Point 140 - 144 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Pka Approximate 8 - 9

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    General Information
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    Frequently Asked Questions

    As a leading 3-Bromo-2-hydroxypyridine 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 3-Bromo-2-hydroxypyridine?
    3-Bromo-2-hydroxypyridine, this is an organic compound. Its physical properties are particularly important and are fundamental to many chemical applications.
    Looking at its appearance, it is usually white to light yellow crystalline powder, just like fine sand, with a pure and soft color. This form is easy to store and use, and is convenient for laboratory operation and industrial production.
    When it comes to the melting point, it is between 146 and 149 ° C. When the temperature gradually rises, the compound gradually melts from the solid state to the liquid state, just like ice and snow melting when warm. The exact value of the melting point is crucial for the identification of its purity. The higher the purity, the closer the melting point approaches the standard value in this range.
    In addition to solubility, it exhibits unique properties in organic solvents. It is easily soluble in halogenated hydrocarbon solvents such as dichloromethane and chloroform, just like fish getting water, and can be uniformly mixed with it. It also has a certain solubility in alcoholic solvents such as methanol and ethanol, but the degree of solubility may vary depending on the characteristics and temperature of the solvent. In water, the solubility is relatively low, and it seems to be slightly estranged from water and only slightly soluble. This difference in solubility provides various possibilities in the separation, purification and reaction medium selection of compounds.
    In addition, 3-bromo-2-hydroxypyridine has a certain stability. At room temperature and pressure, its chemical structure is not easy to change without special chemical reagents or environmental factors. In case of extreme conditions such as strong oxidizing agents or high temperatures, chemical reactions will also occur, resulting in structural changes and subsequent changes in physical properties.
    It can be seen from the above that the physical properties of 3-bromo-2-hydroxypyridine are diverse and unique, laying a solid foundation for its application in many fields such as organic synthesis and drug development.
    What are the chemical properties of 3-Bromo-2-hydroxypyridine?
    3-Bromo-2-hydroxypyridine is one of the organic compounds. Its chemical properties are unique and valuable for investigation.
    Let's talk about its acidity and alkalinity first. Because the molecule contains hydroxyl groups, the oxygen atoms in the hydroxyl groups have lone pairs of electrons, and they are conjugated with the pyridine ring, so that the hydroxyl hydrogen is easy to dissociate, so it has a certain acidity. In the presence of appropriate bases, deprotonation can occur to generate corresponding salts. This is one of its important acid-base properties.
    Let's talk about nucleophilic substitution. Bromine atoms, as a good leaving group, are prone to nucleophilic substitution under suitable nucleophilic reagents and reaction conditions. For example, when there are nucleophiles such as alkoxides, amines, etc., the nucleophilic part of the nucleophilic reagent will attack the carbon atoms connected to the bromine, and the bromine ions will leave, thus forming new compounds. This reaction is widely used in organic synthesis, and can be used to construct various organic molecules of different structures.
    also says its redox properties. The pyridine ring is relatively stable, but under the action of strong oxidants, the pyridine ring may be oxidized, and the hydroxyl group may also be oxidized to other oxygen-containing functional groups such as carbonyl groups. When the reducing agent acts, the pyridine ring or the bromine atom may undergo a reduction reaction, but the specific situation depends on the type of reducing agent and the reaction conditions.
    In addition, 3-bromo-2-hydroxypyridine may also undergo metal-catalyzed reactions. In the presence of transition metal catalysts such as palladium and nickel, it can couple with other organic halides or olefins to form carbon-carbon bonds or carbon-heteroatomic bonds, providing an effective way for the synthesis of complex organic molecules.
    In short, 3-bromo-2-hydroxypyridine is rich in chemical properties and has shown broad application prospects in the fields of organic synthesis and medicinal chemistry, which can help chemists create many novel and valuable organic compounds.
    What are the main uses of 3-Bromo-2-hydroxypyridine?
    3-Bromo-2-hydroxypyridine has a wide range of uses in the field of organic synthesis. First, it can be used as a pharmaceutical intermediate. In the creation of many drugs, it is often relied on as a basis to build a specific molecular structure. Because of its unique structure, it can introduce key groups between reactions, which becomes the cornerstone of building complex drug molecules.
    Furthermore, it is also useful in the field of materials science. For example, it can be used in the preparation of materials with special properties through specific reactions and modifications. Or it can enhance the stability of the material, or it can give it unique optical and electrical properties to meet different needs.
    In addition, in the field of pesticide synthesis, 3-bromo-2-hydroxypyridine is also an important angle. It can be made into a pesticide with high insecticidal, bactericidal or herbicidal properties through a series of chemical transformations. It can precisely act on target organisms, inhibit their physiological processes, and achieve the purpose of preventing and controlling pests.
    In addition, it is also an important model compound in the study of reaction mechanisms in organic synthesis. Chemists can gain insight into the nature and laws of reactions by exploring the reactions they participate in, thus providing a solid theoretical foundation for the development of new synthetic methods and the optimization of reaction conditions. Therefore, 3-bromo-2-hydroxypyridine plays a key role in many fields and is indispensable for chemical research and industrial production.
    What are 3-Bromo-2-hydroxypyridine synthesis methods?
    The synthesis methods of 3-bromo-2-hydroxypyridine are various. One method is to use 2-hydroxypyridine as the starting material, add an appropriate amount of brominating reagent, such as liquid bromine or N-bromosuccinimide (NBS), under suitable reaction conditions, such as in an organic solvent (such as dichloromethane), at low temperature or room temperature, and in the presence of a catalyst (such as Lewis acid, etc.), the bromine atom can replace the hydrogen atom at the 3-position on the pyridine ring to obtain 3-bromo-2-hydroxypyridine. < Br >
    There is another method, using pyridine as the starting material, the hydroxyl group is introduced into the pyridine ring through a specific reaction, and then the bromination reaction is carried out. The hydroxyl group can be introduced by the reaction of pyridine with appropriate electrophilic reagents. This process may be completed under high temperature, high pressure or specific catalyst. Then bromination is carried out, and the conditions are similar to the above, so the target product can also be obtained.
    In addition, other nitrogen-containing heterocyclic compounds can also be used to gradually construct the pyridine ring and introduce hydroxyl and bromine atoms through a series of complex reactions. For example, some five-membered heterocyclic compounds with suitable substituents can finally produce 3-bromo-2-hydroxypyridine through cyclization and functional group transformation. All these methods require fine control of reaction conditions to obtain higher yield and purity.
    What are the precautions in storage and transportation of 3-Bromo-2-hydroxypyridine?
    3-Bromo-2-hydroxypyridine is also an organic compound. During storage and transportation, many matters must be paid attention to.
    First words storage, because it has a certain chemical activity, should be placed in a cool, dry and well ventilated place. If it is in a high temperature, humid environment, or causes deterioration. Keep away from fires and heat sources to prevent danger. Because of its flammability, it may encounter open flames, hot topics or risk of combustion. And should be stored separately from oxidants, acids, bases, etc., to avoid mixed storage. These substances come into contact with it, or cause violent chemical reactions, causing accidents.
    Furthermore, before transportation, make sure that the packaging is complete and sealed. Choose the appropriate means of transportation and follow the relevant regulations. During transportation, be protected from exposure to the sun, rain and high temperature. If it is road transportation, drive according to the specified route and do not stop in densely populated areas and residential areas. When handling, it must also be handled lightly to prevent damage to packaging and containers.
    In short, in the storage and transportation of 3-bromo-2-hydroxypyridine, it is necessary to be careful and follow relevant procedures to ensure the safety of personnel and the integrity of materials.