2 Formyl 5 Bromopyridine
pyridine pyrrole pyrazine piperidine piperazine

2-Formyl-5-Bromopyridine

    Specifications

    HS Code

    402621

    Chemical Formula C6H4BrNO
    Molecular Weight 186.006 g/mol
    Appearance Solid
    Color Off - white to light yellow
    Boiling Point 238 - 240 °C
    Melting Point 54 - 58 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
    Density 1.676 g/cm³
    Flash Point 102.2 °C

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    General Information
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    Frequently Asked Questions

    As a leading 2-Formyl-5-Bromopyridine 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 2-formyl-5-bromopyridine?
    2-% methylpropyl-5-bromopyridine is an organic compound. Its physical properties are unique. Under normal temperature and pressure, it is mostly liquid and has a specific odor. The boiling point and melting point of this substance have certain values. The boiling point is about a certain range, and the melting point is also a specific value. The specific value will vary slightly depending on impurities and measurement conditions.
    Looking at its solubility, 2-% methylpropyl-5-bromopyridine has good solubility in organic solvents such as ethanol and ether, and can be miscible with these solvents in a certain proportion, but the solubility in water is relatively low. This is due to its molecular structure characteristics, containing hydrophobic alkyl and pyridine rings, so the hydrophilicity is not good.
    Its density is also one of the important physical properties. Compared with the density of water, there will be a specific numerical relationship, which has a significant impact in operations such as separation and extraction.
    In terms of appearance, pure 2-% methylpropyl-5-bromopyridine is usually a colorless to light yellow transparent liquid. If there are impurities, the color may change and the appearance may become cloudy.
    Its refractive index is also a parameter characterizing its physical properties. By measuring the refractive index, it can assist in the identification of the purity of the substance and the determination of its molecular structure characteristics.
    In addition, the vapor pressure of 2-% methyl propyl-5-bromopyridine has corresponding values at different temperatures. This property is related to its behavior and volatility in the gas phase, and also affects the requirements of storage and use environments. Understanding the above physical properties is of great significance for the application of 2-% methyl propyl-5-bromopyridine in organic synthesis, pharmaceutical research and development, etc.
    What are the chemical properties of 2-formyl-5-bromopyridine?
    2-% methylpropyl-5-bromopyridine is an organic compound with unique chemical properties. It is active and is a key raw material in many organic reactions.
    First, in the nucleophilic substitution reaction, the bromine atom has high activity and is easily replaced by nucleophilic reagents. In case of alcohol nucleophilic reagents, under alkali catalysis, bromine will be replaced by alkoxy groups to form ether compounds. This reaction principle is that the nucleophilic reagent has a high electron cloud density, attacks the partially positively charged bromine atom, and the bromine ions leave to complete the substitution.
    Second, in the metal-organic reaction, 2-% methylpropyl-5-bromopyridine can interact with metal reagents such as magnesium and lithium to form corresponding organometallic compounds. Taking the reaction with magnesium as an example, in anhydrous ether and other solvents, Grignard reagents are formed. This reagent can participate in a variety of nucleophilic addition and substitution reactions, such as reacting with carbonyl compounds to build new carbon-carbon bonds and enrich the structure of organic compounds.
    Third, it is aromatic. Because the pyridine ring conforms to the Shocker rule, it has a stable conjugate system. This makes it exhibit special properties in some reactions involving aromatic rings, such as electrophilic substitution reactions. Although the activity is weaker than benzene, under suitable conditions, an electrophilic group can be introduced at a specific position of the pyridine ring.
    Fourth, due to the long chain of methyl propyl in the molecule, it has a certain lipid solubility, which affects its solubility in different solvents. It has good solubility in organic solvents such as dichloromethane and chloroform, but poor solubility in water. This solubility difference is extremely important in the separation, purification and reaction system selection of compounds.
    In conclusion, the diverse chemical properties of 2-% methylpropyl-5-bromopyridine provide a powerful tool for the construction of complex organic molecular structures in the field of organic synthesis.
    What is the main use of 2-formyl-5-bromopyridine?
    2-% methylpropyl-5-bromopyridine, although this substance has not been detailed in "Tiangong Kaiji", it can be seen that it has a wide range of uses.
    First, it is often a key intermediate in the field of pharmaceutical synthesis. The structural characteristics of the pyridine ring have good biological activity and adaptability. If you want to make some antibacterial drugs, 2-% methylpropyl-5-bromopyridine can be used as a starting material. After multiple steps of delicate chemical reactions, specific functional groups are introduced to shape the molecular structure that fits the target of bacteria, so as to exert the antibacterial effect.
    Second, it also has its application in the field of materials science. In the synthesis of organic optoelectronic materials, the electron cloud distribution and energy level structure of the material can be adjusted by virtue of its unique chemical structure. In this way, the light absorption and charge transport properties of the material can be optimized, providing assistance for the manufacture of high-performance organic Light Emitting Diodes (OLEDs), solar cells and other materials.
    Third, it is also indispensable in the field of pesticide research and development. After rational molecular design and modification, compounds based on 2-% methylpropyl-5-bromopyridine can exhibit high killing or inhibitory activity against specific pests or weeds. And compared with traditional pesticides, such new pesticides developed based on specific structures may have higher selectivity and environmental friendliness, which can reduce the impact on non-target organisms and reduce environmental pollution.
    In summary, although 2-% methylpropyl-5-bromopyridine was not found in the ancient "Tiangong Kaiwu", it plays a pivotal role in many important fields such as medicine, materials, and pesticides today, and contributes greatly to the development of related industries.
    What are the synthesis methods of 2-formyl-5-bromopyridine?
    To prepare 2-methyl-5-nitropyridine, there are various methods.
    First, pyridine is used as a group to nitrate. In a suitable reaction environment, select suitable nitrifying reagents, such as mixed acid (mixed solution of sulfuric acid and nitric acid), pyridine can undergo electrophilic substitution reaction with nitrate. However, the electron cloud distribution of the pyridine ring is unique, and the nitrogen atom has electron absorption, which makes the electron cloud density on the pyridine ring uneven. The localization selectivity of the nitrification reaction needs to be studied carefully. Usually, the 3-position and 5-position are easier to introduce nitro, but to obtain 2-methyl-5-nitropyridine, the reaction conditions need to be regulated in detail, such as precise temperature control, selection of suitable catalysts, etc., or the reaction can be carried out in the direction of the desired product.
    Second, it can be converted by substituted pyridine derivatives. First, pyridine derivatives with specific substituents, such as 2-methylpyridine. In 2-methylpyridine, methyl is the power supply group, which can affect the electron cloud distribution of the pyridine ring, causing the density of the adjacent and para-potential electron clouds to increase relatively. At this time, the nitration reaction is carried out again. Under suitable conditions, it is easier to introduce nitro at the 5-position, so that the target product can be obtained. This process also requires strict control of the reaction conditions to achieve high yield and high selectivity.
    Third, a synthesis strategy through a multi-step reaction may be considered. Starting from readily available raw materials, the target molecule is constructed through a multi-step functional group transformation, cyclization and other reactions. For example, select a suitable chain compound, form a pyridine ring through condensation and cyclization, and ingeniously introduce methyl and nitro groups. Although there are many steps in this path, the selectivity and controllability of each step of the reaction may be better. By rationally designing the reaction route, it is also expected to produce 2-methyl-5-nitropyridine efficiently.
    All synthesis methods have their own advantages and disadvantages. In actual synthesis, it is necessary to weigh multiple factors such as the availability of raw materials, cost, difficulty in controlling reaction conditions, and purity and yield of the product. The optimal method should be implemented.
    What are the precautions for 2-formyl-5-bromopyridine in storage and transportation?
    2-% methyl-5-nitroimidazole requires attention to many key matters during storage and transportation.
    For storage, one should choose a dry, cool and well-ventilated place. This medicine is prone to moisture and deterioration, and high humidity will cause its chemical properties to change and impair its efficacy. If stored in a humid place, it may agglomerate and decompose. Second, keep away from fire and heat sources. Because of its certain chemical activity, high temperature or open flame may cause combustion or even explosion, as if placed on the edge of danger. Third, it needs to be stored separately from oxidants, acids, etc. Contact with these substances may cause violent chemical reactions, causing accidents. For example, the oxidant meets it, or triggers an oxidation reaction, destroying its structure. Fourth, the storage place should be equipped with the corresponding variety and quantity of fire-fighting equipment and leakage emergency treatment equipment to prepare for emergencies and prevent problems before they occur.
    As for transportation, first of all, the transportation vehicle must be in good condition, with reliable fire and explosion-proof devices, just like a strong fortress, to build a solid foundation for transportation safety. Secondly, the transportation process should be protected from sun exposure, rain and high temperature. Exposure to hot sun and rain may affect the quality of the drug, and high temperature will also make the drug unstable. Furthermore, it should be handled lightly to avoid collisions and heavy pressure. Due to its special nature, severe collisions or heavy pressure may cause packaging damage and drug leakage, which not only wastes and pollutes the environment, but also threatens personnel safety. Finally, transportation personnel need to undergo professional training, be familiar with the characteristics of the drug and emergency treatment methods, and be able to deal with emergencies calmly and avoid danger.