2 Bromo 5 Nitro 3 Trifluoromethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

2-Bromo-5-nitro-3-(trifluoromethyl)pyridine

    Specifications

    HS Code

    633201

    Chemical Formula C6H2BrF3N2O2
    Molar Mass 285.009 g/mol
    Appearance Solid (usually)
    Physical State At Room Temperature Solid
    Solubility In Water Low solubility, as it is an organic halide - nitro - fluorinated compound
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Stability Stable under normal conditions, but can react with strong reducing or oxidizing agents
    Reactivity Reactive towards nucleophiles due to the presence of bromine and nitro groups

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    Frequently Asked Questions

    As a leading 2-Bromo-5-nitro-3-(trifluoromethyl)pyridine 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 main use of 2-Bromo-5-nitro-3- (trifluoromethyl) pyridine?
    2-Bromo-5-nitro-3- (trifluoromethyl) pyridine is a crucial compound in the field of organic synthesis. It has a wide range of uses, especially in the field of pesticide creation. Due to its unique chemical structure, it can derive many pesticide products with high-efficiency insecticidal and bactericidal activities. For example, it can be used as a key intermediate to construct new pyridine pesticides through a series of chemical reactions, showing excellent control effects on common crop pests, ensuring strong crop growth, and improving agricultural yield and quality.
    In the field of pharmaceutical research and development, it also plays a role that cannot be ignored. Studies have shown that compounds containing pyridine structures often have diverse biological activities. 2-Bromo-5-nitro-3- (trifluoromethyl) pyridine can be used as a starting material. After ingenious chemical modification, compounds with specific pharmacological activities can be prepared, providing an important basis for the development of new drugs. It is expected to develop innovative drugs with significant efficacy for specific diseases.
    In addition, in the field of materials science, with its special structure and properties, it can participate in the synthesis of functional materials. For example, by polymerizing with other organic or inorganic monomers, materials with special electrical, optical or thermal properties can be prepared, which can be used in electronic devices, optical coatings and many other aspects to promote technological innovation and development in the field of materials science. Overall, 2-bromo-5-nitro-3- (trifluoromethyl) pyridine has important uses in many fields and has a profound impact on the development of related industries.
    What are the synthesis methods of 2-Bromo-5-nitro-3- (trifluoromethyl) pyridine
    There are several common methods for the synthesis of 2-bromo-5-nitro-3- (trifluoromethyl) pyridine. First, it can be formed by starting from the corresponding pyridine derivative, by a series of reactions such as halogenation, nitration and the introduction of trifluoromethyl. First, take a suitable pyridine substrate, and under suitable conditions, bromide with a brominating reagent. For example, liquid bromine reacts with a pyridine substrate in the presence of a suitable catalyst, allowing bromine atoms to be substituted at specific positions in the pyridine ring.
    Then, nitro is introduced. Mixed acid (a mixture of nitric acid and sulfuric acid) is often used as a nitrifying agent to control the reaction temperature, time and ratio of reactants to introduce nitro into the pyridine ring to obtain brominated nitropyridine intermediates. Finally, with specific reagents and conditions, trifluoromethyl is introduced into this intermediate. Trifluoromethyl-containing reagents can be selected, and nucleophilic substitution or other suitable reaction paths can be used to obtain 2-bromo-5-nitro-3- (trifluoromethyl) pyridine.
    Another way of synthesis is to start with the construction of pyridine rings. With suitable raw materials containing bromine, nitro and trifluoromethyl, the pyridine ring structure is first established through multi-step reaction. For example, with suitable nitrogen-containing compounds, carbonyl compounds and halogenates, through condensation, cyclization and other reactions, the pyridine ring is gradually constructed, and the target substituent is introduced at the same time. During the reaction process, it is necessary to precisely regulate the reaction conditions of each step, such as temperature, pH, reaction time, etc., to ensure that the reaction proceeds according to the expected path and improve the yield and purity of the target product. All synthesis methods have their own advantages and disadvantages. In practical application, when considering factors such as raw material availability, cost, reaction conditions and product purity requirements, the appropriate one is selected.
    What are the physical properties of 2-Bromo-5-nitro-3- (trifluoromethyl) pyridine
    2-Bromo-5-nitro-3- (trifluoromethyl) pyridine, this is a very important compound in the field of organic chemistry. Its physical properties are very interesting, let me tell them one by one.
    Looking at its appearance, under room temperature and pressure, it usually appears as a light yellow to yellow solid. This color state is its externally significant characteristic, like the skin color of a person, which is easy to identify.
    When it comes to the melting point, it is between 56 and 60 degrees Celsius. The melting point is the specific temperature at which a substance changes from a solid state to a liquid state, which is like a door. Across this temperature limit, the form of the substance undergoes wonderful changes. In this temperature range, 2-bromo-5-nitro-3- (trifluoromethyl) pyridine will change from a solid state to a liquid state.
    The boiling point is also one of its important physical properties, which is about 268-270 ° C. At the boiling point, the temperature node at which the liquid converts to a gas. At this time, the molecules in the liquid gain enough energy to break free from the shackles of the liquid phase and escape into the gas phase.
    Furthermore, its density is about 1.92 g/³ cm. Density represents the mass per unit volume of a substance. This value reflects that 2-bromo-5-nitro-3- (trifluoromethyl) pyridine is denser than water. If placed in water, it will sink to the bottom.
    In terms of solubility, the compound is slightly soluble in water. Water is the source of all things, and many substances have different solubility in it. 2-bromo-5-nitro-3- (trifluoromethyl) pyridine has a weak affinity for water, and only a small amount can be dispersed in water. However, it is soluble in organic solvents such as dichloromethane, chloroform, and acetonitrile. Organic solvents are like their close partners, providing them with a suitable dissolution environment. This property is of great significance in organic synthesis and related chemical operations, and is related to the progress of reactions, the separation and purification of products.
    The physical properties of 2-bromo-5-nitro-3- (trifluoromethyl) pyridine play a pivotal role in the research, synthesis and application of organic chemistry, laying the foundation for chemists to explore its chemical mysteries and expand its application range.
    What are the chemical properties of 2-Bromo-5-nitro-3- (trifluoromethyl) pyridine
    2-Bromo-5-nitro-3- (trifluoromethyl) pyridine is an important compound in the field of organic synthesis. Its chemical properties are unique, containing functional groups such as bromine atom, nitro group and trifluoromethyl group, which endow the compound with various reactivity and characteristics.
    First, the bromine atom, which is a good leaving group, can undergo nucleophilic substitution reactions. Under suitable conditions, nucleophiles such as hydroxyl groups and amino groups can replace bromine atoms to form corresponding substitution products. This reaction is quite commonly used in the construction of new carbon-heteroatom bonds, laying the foundation for the synthesis of complex organic molecules. The
    nitro group is also a key functional group. It has strong electron-absorbing properties, which will reduce the electron cloud density of the pyridine ring, making the electrophilic substitution reaction on the pyridine ring more difficult, and the selective change of the reaction check point is more inclined to react at the position where the steric resistance is small and the electron cloud density is relatively high. However, the nitro group can be reduced and can be converted into an amino group after being treated with an appropriate reducing agent, which is of great significance in the preparation of amino-containing pyridine derivatives. Due to the further reaction of the amino group, many compounds with biological activity or special functions can be derived. The introduction of
    trifluoromethyl has greatly changed the physical and chemical properties of the molecule. Due to its strong electron absorption and unique spatial effect, it can significantly improve the lipid solubility and stability of compounds, while affecting the acidity and alkalinity of molecules. In the field of medicinal chemistry, compounds containing trifluoromethyl groups often exhibit good biological activity and metabolic stability, so 2-bromo-5-nitro-3- (trifluoromethyl) pyridine has great application potential in drug synthesis.
    In addition, the electronic structure and aromaticity of the pyridine ring itself enable it to participate in a variety of reactions involving aromatic rings, such as transition metal-catalyzed coupling reactions, which provide the possibility for the construction of more complex polycyclic or fused ring systems, and also have potential applications in materials science, pesticide chemistry and other fields.
    What is the price range of 2-Bromo-5-nitro-3- (trifluoromethyl) pyridine in the market?
    In my opinion, it is not easy to know the price range of 2 - Bromo - 5 - nitro - 3 - (trifluoromethyl) pyridine in the market. Due to the complex and changeable market conditions, its price is often influenced by many factors.
    The first to bear the brunt is the difficulty of production. If the synthesis process of this compound is complicated, and the requirements for raw materials, equipment and technology are quite high, the cost will increase, and the price will also be high. On the contrary, if the process is simple, the cost is controllable, and the price may be relatively low.
    Furthermore, the market supply and demand situation has a great impact. If there are many people in need, but the quantity produced is small, the supply is in short supply, and the price will rise; if there is an oversupply, the merchant will sell the goods or reduce the price.
    In addition, the price of raw materials also affects its price. If raw materials are scarce or expensive, the price of 2-Bromo-5-nitro-3 - (trifluoromethyl) pyridine obtained based on this is bound to rise.
    In addition, factors such as manufacturer brand and product purity should not be underestimated. Well-known manufacturers and high-purity products often have high prices; those produced by small factories with slightly lower purity may have low prices.
    However, it is difficult to determine its exact price range after searching for past market information. Roughly speaking, in the chemical raw material market, the price of such fine chemicals varies greatly. If it is ordinary purity, the price per gram may be between tens of yuan and 100 yuan; if the purity requirements are extremely high, the price per gram may exceed 100 yuan or even higher, up to hundreds of yuan per gram. However, this is only a rough guess, and the actual price still needs to be consulted with chemical product suppliers, subject to real-time quotations.