2 Bromo 6 Hydroxypyridine
pyridine pyrrole pyrazine piperidine piperazine

2-Bromo-6-hydroxypyridine

    Specifications

    HS Code

    750732

    Chemical Formula C5H4BrNO
    Molar Mass 172.00 g/mol
    Appearance Solid (presumed, typical for many small organic compounds)
    Solubility In Water Low solubility expected due to non - polar aromatic part and limited polarity from Br and OH
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone, dichloromethane
    Pka Of Hydroxyl Group Approx. 9 - 10 (phenol - like group)
    Odor Odorless or faint organic odor (speculative, typical for many simple heterocyclic compounds)

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    General Information
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    Frequently Asked Questions

    As a leading 2-Bromo-6-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 chemical properties of 2-Bromo-6-hydroxypyridine?
    2-Bromo-6-hydroxypyridine, this is an organic compound with a variety of unique chemical properties. In its molecular structure, bromine atoms and hydroxyl groups are attached to specific positions of the pyridine ring, which has a great impact on its chemical activity.
    The presence of phenolic hydroxyl groups makes the compound acidic. The phenolic hydroxyl groups can dissociate protons and react with bases to form corresponding salts. This property is often used in organic synthesis to form specific ionic bonds or for the separation and purification of compounds. For example, if it is placed in an alkaline aqueous solution, the phenolic hydroxyl groups will react with bases, causing the compound to dissolve in the aqueous phase, thereby achieving separation from other water-insoluble impurities.
    Furthermore, bromine atoms are active substituents and are prone to nucleophilic substitution reactions. The characteristics of halogenated hydrocarbons make bromine atoms can be replaced by a variety of nucleophilic reagents, such as alcohols and amines. If alcohols are used as nucleophiles, bromine atoms will be replaced by alkoxy groups under suitable conditions to form ether compounds. This reaction is widely used in the preparation of new ether derivatives containing pyridine structures, which can effectively expand the structural diversity of compounds.
    The pyridine ring itself also endows the compound with special properties. Pyridine rings have certain aromatic properties, making them relatively stable, and can also participate in intermolecular interactions such as π-π stacking. In the crystal structure or solution, this interaction affects the physical properties of the compound such as melting point and solubility. In addition, the lone pair electrons of the nitrogen atom of the pyridine ring can be used as electron donors to form coordination bonds with metal ions. This property is widely used in the field of metal organic chemistry and can be used to prepare metal complexes. These complexes exhibit unique properties in catalysis and materials science.
    In addition, there may be hydrogen bonding between the hydroxyl groups in the 2-bromo-6-hydroxypyridine molecule and the pyridine ring, which has an important impact on the conformation and stability of the molecule. Intramolecular hydrogen bonding can cause molecules to form specific spatial structures, which in turn affect their chemical activity and physical properties. In chemical reactions, the stability of the molecular conformation affects the exposure of the reaction check point, thereby affecting the reaction rate and selectivity.
    What is 2-Bromo-6-hydroxypyridine synthesis method?
    The synthesis of 2-bromo-6-hydroxypyridine is an important topic in the field of organic synthesis. The synthesis of this compound is often achieved by a multi-step reaction using pyridine as the starting material.
    In the first step, the pyridine can be first hydroxylated to introduce a hydroxyl group at its position 6. The method of hydroxylation can use a nucleophilic substitution reaction. For example, pyridine is reacted with a suitable nucleophilic reagent under suitable reaction conditions. The nucleophilic reagent can be selected with negative ions containing hydroxyl groups. In an alkaline environment, the nucleophilic reagent attacks the pyridine ring to form 6-hydroxypyridine. In this step, the reaction temperature, time and the proportion of reactants need to be carefully adjusted to ensure that the reaction proceeds smoothly and the yield is good.
    In the next step, the obtained 6-hydroxypyridine is brominated, and bromine atoms are introduced at position 2. A variety of bromination reagents can be selected for the bromination reaction, such as liquid bromine, N-bromosuccinimide (NBS), etc. If NBS is selected as the bromination reagent, it is usually reacted in an organic solvent under the action of an initiator. The initiator can prompt NBS to generate bromine radicals, which in turn undergoes radical substitution reaction with 6-hydroxypyridine, introducing bromine atoms at position 2 to form the target product 2-bromo-6-hydroxypyridine. In this step, attention should also be paid to the control of reaction conditions to prevent side reactions from occurring, such as the formation of polybrominated products.
    Another synthesis path can be used. Pyridine can be brominated first, bromine atoms are introduced at position 2, and then hydroxylated to introduce hydroxyl groups at position 6. However, this path needs to consider the influence of bromine atoms on subsequent hydroxylation reactions, because it may change the electron cloud density of the pyridine ring, which affects the activity and selectivity of nucleophilic substitution reactions. < Br >
    To synthesize 2-bromo-6-hydroxypyridine, the optimization of reaction conditions at each step is extremely critical, and strict monitoring of the reaction process is required to obtain the ideal yield and purity.
    What are the main uses of 2-Bromo-6-hydroxypyridine?
    2-Bromo-6-hydroxypyridine is widely used in the field of organic synthesis. First, it is used as a pharmaceutical intermediate. In the process of creating drugs, it can be derived from a variety of biologically active compounds. For example, when developing antibacterial drugs, its structure can be cleverly modified and integrated into the molecular structure of the drug, giving the drug unique antibacterial efficacy. By combining with specific targets in bacteria, it can block their normal physiological activities and achieve the purpose of antibacterial.
    In addition, it also plays an important role in the field of pesticide synthesis. After proper chemical transformation, it can be converted into key components of pesticides. For example, the preparation of some new insecticides, 2-bromo-6-hydroxypyridine, through a series of reactions, produces substances with high insecticidal activity, which can precisely act on specific physiological links of pests, such as interfering with the signal transduction of the pest's nervous system, causing behavioral disorders and eventually death, providing a powerful means for agricultural pest control.
    In addition, in the field of materials science, it can also play a role. When preparing specific functional materials, it can be introduced into the material system as a structural unit. For example, when synthesizing optoelectronic functional materials, its special structure and electronic properties can improve the photoelectric properties of the materials, such as improving the fluorescence quantum yield of the materials and optimizing the charge transport capacity, so as to meet the strict requirements of optoelectronic devices on material properties. Overall, 2-bromo-6-hydroxypyridine has important uses in many fields and is an indispensable raw material for the development of chemical synthesis and related industries.
    What are the precautions in storage and transportation of 2-Bromo-6-hydroxypyridine?
    For 2-bromo-6-hydroxypyridine, many things should be paid attention to during storage and transportation.
    Its chemical properties are active and it is easy to react with many substances. When storing, the first environment is dry. Moisture can easily deteriorate it, so it must be stored in a dry place, away from water sources and humid places.
    Furthermore, temperature is also crucial. This substance is quite sensitive to temperature, and either too high or too low temperature may affect its stability. It should be stored in a cool place, the temperature should be controlled within a specific range, and it should not be placed in a high temperature or sun exposure to avoid adverse changes such as decomposition.
    Packaging must be tight. Because it has certain volatility and reactivity, if the packaging is not strict, it is easy to leak and react with external substances. Use a well-sealed container to ensure that there is no risk of leakage.
    During transportation, it is crucial to prevent shock and collision. Because it is a chemical substance, bumps and vibrations or damage to the package, which in turn causes leakage. The means of transportation should run smoothly and properly fix the goods.
    In addition, it needs to be stored and transported separately from other chemicals. Because it may react violently with certain substances, it is easy to cause danger when mixed. Chemicals of different properties should be classified and disposed of to ensure the safety of transportation and storage. In conclusion, the storage and transportation of 2-bromo-6-hydroxypyridine requires caution and strict follow-up to ensure its quality and safety.
    What is the market price of 2-Bromo-6-hydroxypyridine?
    2-Bromo-6-hydroxypyridine, an important compound in organic chemistry, is widely used in many fields such as pharmaceuticals and materials science. As for its market price, it is difficult to give an exact figure, because it is affected by the interaction of many factors.
    First, the market supply and demand relationship is the key factor. If the market demand for 2-bromo-6-hydroxypyridine is strong, but the supply is relatively insufficient, the price will rise; conversely, if the supply exceeds the demand, the price will inevitably fall. For example, if the demand for a new drug in the pharmaceutical industry increases sharply, and the manufacturer fails to expand production capacity in time, the price will rise in this situation.
    Second, the cost of production also affects the price. The cost of raw materials, the complexity of the production process and energy consumption are all cost components. If raw materials are scarce and expensive, or the production process requires complex processes and high-end equipment, the cost is bound to increase, and the price will also rise.
    Third, the price varies depending on the manufacturer. Well-known large factories may have high prices due to strict product quality control and good reputation; while some small factories may compete with low-price strategies in order to seek market share.
    Fourth, the sales region and purchase volume also affect the price. Different regions have different prices due to differences in economic level, logistics costs, etc.; bulk purchases can often get preferential prices.
    According to past market conditions and comprehensive consideration of various factors, the price of 2-bromo-6-hydroxypyridine fluctuates greatly, ranging from tens to hundreds of yuan per gram. However, this is only a rough estimate. The actual price must be checked in real time on the chemical product trading platform and supplier quotations to accurately grasp.