5 Amino 2 Bromo 3 Chloropyridine
pyridine pyrrole pyrazine piperidine piperazine

5-Amino-2-bromo-3-chloropyridine

    Specifications

    HS Code

    482027

    Name 5 - Amino - 2 - bromo - 3 - chloropyridine
    Molecular Formula C5H4BrClN2
    Molecular Weight 207.46
    Appearance Solid (usually)
    Physical State Solid at room temperature
    Solubility Solubility in common solvents like ethanol, dichloromethane etc. would need specific data
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

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    General Information
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    Frequently Asked Questions

    As a leading 5-Amino-2-bromo-3-chloropyridine 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 chemistry of 5-Amino-2-bromo-3-chloropyridine?
    5-Amino-2-bromo-3-chloropyridine, this is an organic compound. Its chemical properties are unique and interesting.
    First of all, its physical properties are mostly solid at room temperature, but the specific melting point varies depending on the preparation method and purity.
    In terms of chemical activity, the presence of amino groups gives it alkalinity. Nitrogen atoms in amino groups have lone pairs of electrons, which can react with acids to form corresponding salts. This property can be used in organic synthesis to separate and purify the compound, or to participate in many nucleophilic substitution reactions.
    Furthermore, the bromine atom at position 2 and the chlorine atom at position 3 are both halogen atoms. Halogen atoms are highly active and prone to nucleophilic substitution reactions. Under appropriate reaction conditions, such as the presence of strong bases and heating, bromine or chlorine atoms can be replaced by other nucleophilic reagents, thus introducing new functional groups, which greatly expands the derivatization ability of the compound. This reaction mechanism is that the nucleophilic reagent attacks the carbon atom connected to the halogen atom, and the halogen atom leaves with a pair of electrons to complete the substitution process.
    In addition, the conjugated system of the pyridine ring makes the compound stable to a certain extent. However, this conjugated system also affects the distribution of its electron cloud, resulting in different reactivity at different positions on the ring. Usually, the electron cloud density of the α and γ positions of the pyridine ring is relatively low, which is more prone to electrophilic substitution reactions; while the electron cloud density of the β position is relatively high, and nucleophilic substitution reactions are more likely to occur at the β position. In 5-amino-2-bromo-3-chloropyridine, the substitution position of the amino group and the halogen atom has a profound impact on its reactivity and selectivity.
    It has a wide range of uses in the field of organic synthesis and can be used as a key intermediate for the preparation of various drugs, pesticides and functional materials. For example, by cleverly selecting reaction reagents and conditions, and using the substitution reaction of halogen atoms, more complex organic molecular structures can be constructed to meet the needs of different fields.
    What are the main uses of 5-Amino-2-bromo-3-chloropyridine?
    5-Amino-2-bromo-3-chloropyridine is an organic compound with a wide range of uses. In the field of medicinal chemistry, it is often a key intermediate for the synthesis of drugs. The structure of the geinpyridine ring exists in many drug molecules, and the amino group, bromine atom and chlorine atom on the compound can be introduced into other functional groups through various chemical reactions to construct drug molecules with specific biological activities.
    It also has important applications in the field of pesticide chemistry. Using it as a raw material, pesticides with insecticidal, bactericidal or herbicidal effects can be prepared through a series of reactions. Due to its unique chemical structure, it may give pesticides a unique mechanism of action, enhancing the activity of target organisms and reducing the impact on non-target organisms.
    In the field of materials science, 5-amino-2-bromo-3-chloropyridine also shows potential. For example, it can participate in the synthesis of functional materials, such as organic semiconductor materials. By rationally designing the reaction, it can be introduced into the polymer structure, which may endow the material with unique electrical and optical properties, and can be used in devices such as organic Light Emitting Diodes and field effect transistors.
    In addition, in organic synthetic chemistry, it can be used as an important intermediate to construct more complex organic molecular structures. Chemists can use the different reactivity of amino, bromine and chlorine to selectively carry out substitution, coupling and other reactions to achieve precise regulation of molecular structure and synthesize organic compounds with special structures and properties.
    In summary, 5-amino-2-bromo-3-chloropyridine has important uses in many fields such as medicine, pesticides, materials and organic synthesis, providing a key chemical basis for the development of related fields.
    What is 5-Amino-2-bromo-3-chloropyridine synthesis method?
    The synthesis of 5-amino-2-bromo-3-chloropyridine is an important topic in the field of organic synthesis. Its synthesis path requires subtle chemical means, specific starting materials, and reasonable reaction steps.
    Pyridine is often used as the starting material because it has a suitable skeleton structure. Halogen atoms are introduced into the pyridine ring before, which can be achieved by halogenation reaction. If you want to introduce bromine atoms, you can choose suitable brominating reagents, such as liquid bromine or N-bromosuccinimide (NBS). Under appropriate reaction conditions, such as specific temperatures and catalysts, bromine atoms can be selectively attached to a specific position of the pyridine ring, that is, the 2-position.
    After the bromine atom is introduced, the chlorination reaction is carried out. A suitable chlorination reagent, such as chlorine gas or phosphorus trichloride, can be used to connect the chlorine atom to the 3-position of the pyridine ring under appropriate conditions.
    However, this process requires fine regulation of the reaction conditions. Due to the selectivity and activity of the halogenation reaction, it is affected by many factors such as temperature, solvent, and catalyst. If the temperature is too high or too low, side reactions may occur, or the reaction rate is poor. After the halogen atom is introduced, an amination reaction is carried out to introduce an amino group. Ammonia or suitable amination reagents can be selected. In an appropriate reaction system, the amino group is substituted for the atom or group at a specific position on the pyridine ring to obtain 5-amino-2-bromo-3-chloropyridine. This process also requires attention to the control of reaction conditions to ensure that the amination reaction is carried out efficiently and selectively. < Br >
    Synthesis of this compound requires careful operation and precise control of conditions at each step to improve the yield and purity of the target product, which is the key to synthesizing this compound.
    5-Amino-2-bromo-3-chloropyridine What are the precautions during storage and transportation?
    5-Amino-2-bromo-3-chloropyridine is one of the organic compounds. During storage and transportation, many matters need to be paid attention to.
    First talk about storage. This compound should be placed in a cool and dry place, away from fire and heat sources. Because of its certain chemical activity, it is dangerous to be heated or exposed to open flames, causing chemical reactions to be disordered, and even causing fire or explosion. Furthermore, the storage environment should be well ventilated to prevent the accumulation of harmful gases. The cover may evaporate harmful gases. If the ventilation is not smooth, it will damage human health and the environment.
    Storage containers are also crucial. It must be made of corrosion-resistant materials, such as glass or containers made of certain plastic materials. Due to the chemical properties of 5-amino-2-bromo-3-chloropyridine, or the reaction with certain materials, the container will be damaged and the compound will leak. And the container must be tightly sealed to avoid contact with air and moisture. Air and moisture may cause oxidation, hydrolysis and other reactions, which affect its chemical purity and stability.
    As for transportation, the first thing is to follow relevant regulations and standards. Transportation personnel should be familiar with the characteristics and safety precautions of this compound and should only be trained professionally. During transportation, it is also necessary to ensure its stability and avoid violent vibration and collision. Compound leakage due to vibration and collision or rupture of the container. If transported in a vehicle, the vehicle should be equipped with necessary safety equipment, such as fire extinguishers, leakage emergency treatment tools, etc. Once a leak occurs, it can be responded to in time to reduce the harm.
    In short, 5-amino-2-bromo-3-chloropyridine needs to be treated with caution during storage and transportation, from the environment, containers to personnel operation and safety equipment, to ensure safety and avoid disasters.
    What is the market outlook for 5-Amino-2-bromo-3-chloropyridine?
    5-Amino-2-bromo-3-chloropyridine is an important chemical substance in the field of organic synthesis. Looking at its market prospects, it needs to be reviewed in detail from many aspects.
    From the perspective of pharmaceutical research and development, such pyridine derivatives often have unique biological activities and are often used as key intermediates when creating new drug molecules. Today, the pharmaceutical industry has an increasing demand for highly effective and specific drugs, and the development of new antimicrobial, anticancer and neurological drugs has become a general trend. 5-Amino-2-bromo-3-chloropyridine has broad prospects in the pharmaceutical intermediates market due to its special structure, which may provide a novel structural framework for the design of new target drugs.
    In the field of materials science, with the vigorous development of organic electronic materials research, nitrogen-containing heterocyclic compounds have attracted extensive attention due to their good photoelectric properties. 5-Amino-2-bromo-3-chloropyridine, after appropriate chemical modification, may be applied to the preparation of organic Light Emitting Diode (OLED), organic solar cells and other materials, which is also one of the potential directions for its market expansion.
    However, its market development also faces several challenges. The complexity of the synthesis process is a major obstacle. The preparation of this compound often requires multi-step reactions, and many harsh reaction conditions and expensive reagents are involved, which makes the production cost high and restricts large-scale production and marketing activities. In addition, the global chemical market is highly competitive, and there are many similar or alternative compounds. If you want to occupy a place in the market, you need to continuously improve product quality and optimize production processes to reduce costs.
    Overall, although 5-amino-2-bromo-3-chloropyridine shows potential application value in the field of medicine and materials due to its unique structure, it is necessary to overcome many difficulties such as synthesis cost and competitive pressure in order to fully tap the market potential. With time, we can overcome the problem and usher in a broader market prospect.