3 Pyridinecarboxaldehyde 2 Bromo 4 Chloro
pyridine pyrrole pyrazine piperidine piperazine

3-Pyridinecarboxaldehyde, 2-bromo-4-chloro-

    Specifications

    HS Code

    395509

    Chemical Formula C6H3BrClNO
    Molecular Weight 220.45
    Appearance Solid (likely, based on similar compounds)
    Physical State At Room Temperature Solid
    Solubility In Water Low (aromatic and halogen - containing, limited H - bonding with water)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Odor Characteristic aldehyde - like odor (possibly pungent)
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents

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    Frequently Asked Questions

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    3-Pyridinecarboxaldehyde, what are the chemical properties of 2-bromo-4-chloro-
    3-Pyridyl formaldehyde, 2-bromo-4-chlorine, is a kind of organic compound. Its physical properties, at room temperature, are either solid or liquid, depending on its intermolecular forces and lattice structure. Looking at its color, it is colorless and transparent, or has a light hue, which is related to the electron transition and conjugation system in the molecule. Smell, or has a special odor, which is given by its functional group and molecular configuration.
    When it comes to chemical properties, aldehyde is one of its activity check points. The aldehyde group has strong reductivity and can react with many oxidants. In case of weak oxidants, such as Torun reagent, a silver mirror reaction can occur, and the aldehyde group is oxidized to a carboxyl group. This is a typical reaction of aldehyde compounds, which originates from the activity of the aldehyde group carbon-hydrogen bond. In case of strong oxidants, such as potassium permanganate, the aldehyde group is also oxidized, and the product may be a carboxylic acid. The degree of reaction is closely related to the conditions.
    Furthermore, the presence of halogen atoms also gives it unique chemical properties. 2-Bromine and 4-chlorine atoms can undergo substitution reactions under appropriate conditions. Nucleophiles can attack the carbon atoms attached to the halogen atom, and the halogen atom leaves as a leaving group to achieve substitution. This is because the electronegativity of the halogen atom is large, so that the attached carbon atoms are partially positively charged and vulnerable to attack by nucleoph In addition, the electron cloud distribution and aromaticity of the pyridine ring also affect the reactivity and selectivity of the compound, making it potentially valuable in the field of organic synthesis.
    3-Pyridinecarboxaldehyde, what are the common synthesis methods of 2-bromo-4-chloro-
    The common synthesis methods of 3-pyridine formaldehyde and 2-bromo-4-chlorine are as follows:
    First, the corresponding pyridine derivative is used as the starting material. Suitable 2-position and 4-position pyridine compounds with convertible groups can be found. By halogenation reaction, the 2-position is introduced into the bromine atom and the 4-position is introduced into the chlorine atom. This halogenation reaction requires the selection of appropriate halogenation reagents, such as liquid bromine, N-bromosuccinimide (NBS), etc.; chlorine gas and phosphorus oxychloride can be selected as the chlorination agent. When reacting, it is necessary to pay attention to the control of reaction conditions, such as temperature, reaction time, solvent selection, etc. If NBS is used as a brominating agent, carbon tetrachloride is often used as a solvent, and the reaction under the condition of heating and reflux can selectively replace the bromine atom at the target position.
    Second, 2-bromo-4-chloropyridine can also be synthesized first, and then an aldehyde group can be introduced at the 3-position of the pyridine. To introduce an aldehyde group, the common method is through the Vilsmeier-Haack reaction. 2-Bromo-4-chloropyridine is co-heated with N, N-dimethylformamide (DMF) and phosphorus oxychloride to form an intermediate of Vilsmeier reagent, and then hydrolyzed to generate an aldehyde group at the 3-position. This reaction process is critical to the control of reaction temperature and time. If the temperature is too high or the time is too long, it may cause more side reactions and affect the yield and purity of the product.
    Third, there is another coupling reaction route catalyzed by metal. First, pyridine metal reagents containing specific substituents, such as lithium pyridine reagent or pyridine Grignard reagent, are prepared, and then coupled with the corresponding halogenated aldehyde. This method requires a strict anhydrous and oxygen-free reaction environment, and the preparation of metal reagents also requires fine operation to ensure the smooth progress of the reaction and the good yield of the product.
    When synthesizing 3-pyridyl formaldehyde and 2-bromo-4-chlorine, the appropriate synthesis method should be carefully selected according to the availability of starting materials, the difficulty of controlling the reaction conditions, cost and many other factors, and the reaction parameters should be carefully adjusted during the reaction process to achieve the best synthesis effect.
    3-Pyridinecarboxaldehyde, where is 2-bromo-4-chloro-used?
    3-Pyridine formaldehyde and 2-bromo-4-chlorine are useful in various fields. They are key raw materials in the field of pharmaceutical creation. The structural characteristics of pyridine, bromine and chlorine endow the compounds with unique activities, which can pave the way for the development of new drugs, or help the development of antibacterial, antiviral and even anti-cancer drugs.
    In the field of materials science, it also has potential. With its special chemical structure, it may be able to participate in the synthesis of materials with special properties, such as photoelectric materials. With its introduction, it may be able to optimize the properties of light absorption and charge transfer of materials, and play a role in improving performance in the manufacturing of Light Emitting Diode, solar cells and other devices.
    In the field of organic synthesis chemistry, its role cannot be underestimated. As an important intermediate, it can undergo various chemical reactions to derive many complex organic compounds. Chemists can expand the library of organic molecules by modifying its structure, providing rich materials and opportunities for exploring new chemical substances and reaction mechanisms.
    Due to its unique structure and chemical properties, this compound has the potential to play an important role in many fields such as medicine, materials and organic synthesis, just like a key to open many scientific explorations and applications.
    3-Pyridinecarboxaldehyde, what is the market price of 2-bromo-4-chloro-?
    "3 - Pyridinecarboxaldehyde, 2 - bromo - 4 - chloro -" is an organic compound. However, it is not easy to know its market price. The price of this compound often changes due to various factors.
    First, the price of raw materials fluctuates, and its cost has a great impact. If the price of raw materials for this compound rises and falls suddenly, the price of the finished product also fluctuates.
    Second, the difficulty of preparation also affects its price. If the preparation method is complicated, requires exquisite craftsmanship, expensive equipment, and the output is limited, the price will be high; on the contrary, if the preparation is easy and the output is considerable, the price may be easy.
    Third, the supply and demand relationship in the market is the key to the price. If there are many people who need this compound, but the supply is insufficient, the price will rise; if the supply exceeds the demand, the price will tend to fall.
    Fourth, the difference in manufacturers also leads to different prices. The technology, scale, and operating costs of each manufacturer are different, and the price set is also different.
    In the era of "Tiangong Kaiwu", although there is no definite price of such compounds, the reason for everything described in it is also applicable here. To know the market price of this "3-Pyridinecarboxaldehyde, 2-bromo-4-chloro-", you need to carefully observe the dynamics of the chemical market, consult industry experts, or refer to the data of relevant trading platforms to obtain a more accurate price.
    3-Pyridinecarboxaldehyde, what are the storage conditions for 2-bromo-4-chloro-?
    The storage conditions of 3-pyridyl formaldehyde and 2-bromo-4-chlorine are also crucial. This material is special, and if it is not properly stored, it may deteriorate, damage its effectiveness, or risk safety.
    It is better to keep it in a cool and dry place, away from direct sunlight. Hot sunlight can promote its chemical reactions and cause changes in its composition. A cool place with a constant temperature can keep its chemical properties stable. A dry environment is also essential, and moisture is easy to cause hydrolysis or other adverse reactions, so the storage place must be protected from moisture.
    Furthermore, its storage is suitable for sealed devices. Exposed to the air, it is easy to interact with various components in the air, such as oxygen, carbon dioxide, etc. A sealed device can block the entry of air and keep it pure.
    It should also be placed separately from other chemicals. Different chemicals have different properties. If they are mixed in one place, or react violently, it will cause disaster. The 3-pyridine formaldehyde and 2-bromo-4-chlorine must be stored in accordance with the above storage conditions to maintain their quality for future use. And the storage place should be guarded by a special person and inspected frequently. If there is any abnormality, they should be disposed of quickly to obtain complete results.