2 Pyridinecarbonitrile 5 Nitro 3 Trifluoromethyl
pyridine pyrrole pyrazine piperidine piperazine

2-Pyridinecarbonitrile, 5-nitro-3-(trifluoromethyl)-

    Specifications

    HS Code

    289151

    Chemical Formula C7H2F3N3O2
    Molar Mass 217.105 g/mol
    Appearance Solid (predicted)
    Boiling Point 326.9 °C at 760 mmHg (predicted)
    Melting Point 107 - 111 °C
    Density 1.606 g/cm³ (predicted)
    Flash Point 151.5 °C (predicted)
    Water Solubility Insoluble (predicted)
    Logp 2.31 (predicted)
    Pka 0.61±0.10 (predicted)

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    Frequently Asked Questions

    As a leading 2-Pyridinecarbonitrile, 5-nitro-3-(trifluoromethyl)- supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    2-Pyridinecarbonitrile, what are the chemical properties of 5-nitro-3- (trifluoromethyl) -
    2-Pyridineformonitrile, 5-nitro-3- (trifluoromethyl), is one of the organic compounds. Its physical properties are mostly solid at room temperature, and the color is either white or nearly white, and the powder is common. This substance has a specific melting point, but the exact value varies depending on the purity. It has a certain solubility in organic solvents, such as common ethanol and dichloromethane, but its solubility in water is quite small.
    When it comes to chemical properties, it is active because its structure contains cyano (-CN), nitro (-NO 2) and trifluoromethyl (-CF). The cyanyl group can be hydrolyzed to form a carboxyl group (-COOH), or reduced to an amino group (-NH2O). Nitro is a strong electron-absorbing group, which reduces the electron cloud density of the pyridine ring, making the electrophilic substitution reaction difficult, but making the nucleophilic substitution reaction easy. Trifluoromethyl has strong electronegativity and hydrophobicity, which not only affects the polarity of the molecule, but also plays a great role in the reactivity and selectivity. This compound may be involved in organic synthesis, in the field of drug development, materials science, or as a key intermediate. It can be reacted in multiple steps to construct complex and functional molecular structures.
    2-Pyridinecarbonitrile, what are the main uses of 5-nitro-3- (trifluoromethyl) -
    2-Pyridineformonitrile, 5-nitro-3- (trifluoromethyl) This substance has a wide range of uses. In the field of pharmaceutical synthesis, it is often a key intermediate. With this substance, a variety of drugs with unique curative effects can be prepared through various delicate chemical reactions, or used to treat difficult diseases, or as a medicine to relieve common pain.
    It can also be seen in the field of materials science. Its unique chemical structure can give materials different properties. By ingeniously fusing with other substances, it can improve the stability of the material and make it durable in changing environments; or it can enhance the special functions of the material, such as electrical conductivity, optical properties, etc., so as to meet the strict needs of high-performance materials in electronic, optical and other industries.
    In the industry of pesticide research and development, 2-pyridyl formonitrile, 5-nitro-3 - (trifluoromethyl) also play an important role. Based on it, it can create efficient pesticides, kill pests precisely, and reduce the impact on the environment to a low degree, help agriculture produce a lot, and protect the ecological balance. This is its main use, and it has outstanding performance in many fields, making great contributions to human production and life.
    2-Pyridinecarbonitrile, what is the synthesis method of 5-nitro-3- (trifluoromethyl) -
    To prepare 2-pyridyl methanonitrile, 5-nitro-3- (trifluoromethyl), the method is as follows. The compound containing the pyridine structure is often used as the starting material and is delicately converted through several steps.
    The first step is to find a suitable pyridine derivative, which needs to have a modifiable check point and skillfully react with the nitro introduction reagent. The method of nitro introduction is to rely on the nitrification reaction. In a specific reaction medium, the temperature is controlled and controlled, so that the nitro group precisely falls at the 5-position of the pyridine ring. This reaction requires strict reaction conditions. If the temperature is high, it is easy to cause a cluster of side reactions, and if the temperature is low, the reaction is slow and difficult to progress. The choice of medium is also crucial, and it needs to have good compatibility with the reactants and reagents without interfering with the reaction process.
    Then, trifluoromethyl is introduced. This step is also not easy. You can choose a suitable trifluoromethylation reagent, and with the help of a catalyst, the trifluoromethyl is connected to the 3-position of the pyridine ring. The choice of catalyst is related to the rate and selectivity of the reaction. High-quality catalysts can accelerate the reaction and guide the precise binding of trifluoromethyl to reduce unnecessary by-products.
    At the end, the specific position of the pyridine ring is converted into a nitrile group through nitrile reaction, and the final product is 2-pyridyl formonitrile, 5-nitro-3 - (trifluoromethyl). This step requires controlling the reaction conditions, the amount of nitrile reagents, and the pH of the reaction environment, which all have a profound impact on the purity and yield of the product. After each step of the reaction, it needs to be separated and purified to remove impurities and retain essence to achieve high purity of the product. The steps are interconnected, and any slight error in any link may cause the product to fail to meet expectations.
    2-Pyridinecarbonitrile, 5-nitro-3- (trifluoromethyl) - what are the precautions during storage and transportation
    2-Pyridineformonitrile, 5-nitro-3- (trifluoromethyl) This material needs to be paid attention to during storage and transportation.
    Its chemical properties are relatively active, and the first environment is dry during storage. Moisture is easy to cause reactions such as hydrolysis, resulting in quality deterioration. The humidity in the warehouse should be controlled within a specific range, such as the relative humidity does not exceed 60%. And it should be placed in a cool place, away from heat and fire sources. Because it is easy to decompose when heated, it is even dangerous to explode. The temperature should be maintained between 15 ° C and 30 ° C.
    Furthermore, it should be stored in isolation. Do not store with oxidants, acids, bases, etc. Because of its nitrile, nitro and trifluoromethyl groups, it is easy to react violently when exposed to oxidants or acid and alkali.
    When transporting, the packaging must be solid. Select special chemical packaging materials to prevent leakage, collision and damage. Transportation vehicles should be equipped with fire and emergency treatment equipment to prepare for emergencies. During transportation, avoid high temperature periods and bad road conditions. In case of rollover, leakage, etc., drivers and passengers should evacuate as soon as possible and deal with them according to emergency plans to prevent pollution and accident expansion. In short, all aspects of storage and transportation of 2-pyridinonitrile, 5-nitro-3- (trifluoromethyl) should be prudent, strictly abide by norms, and ensure the safety of personnel and the environment.
    2-Pyridinecarbonitrile, 5-nitro-3- (trifluoromethyl) - What are the effects on the environment and human health?
    2-Pyridineformonitrile, 5-nitro-3- (trifluoromethyl) This substance has a significant impact on the environment and human health. Here's a detailed analysis.
    In terms of the environment, it may pose multiple hazards. If this substance flows into natural water bodies, it accumulates in the water body due to its special chemical structure or difficulty to be easily decomposed by microorganisms. Once aquatic organisms are exposed to or poisoned. For example, fish contact with water bodies containing this substance may cause physiological disorders, affecting their reproduction, growth, and even death, thereby destroying the balance of aquatic ecosystems.
    In the soil environment, it may change the physical and chemical properties of the soil and affect the community structure and function of microorganisms in the soil. Soil microorganisms are crucial to soil fertility and material circulation. Once they are disturbed, they will affect plant growth, affect crop yield and quality, and then cause a chain reaction to the entire terrestrial ecosystem.
    There are also many hidden dangers to human health. If the human body ingests through breathing, skin contact or accidental ingestion, groups such as nitro and trifluoromethyl may interfere with the normal physiological and biochemical processes of the human body. After entering the human body, it may damage important organs such as the liver and kidneys. The liver is the hub of detoxification in the human body, and the kidneys are responsible for excreting waste. This substance may interfere with its normal metabolic function, causing toxins to accumulate in the body and causing organ diseases.
    Furthermore, this substance may be potentially carcinogenic. Although there is no conclusive conclusion, according to the study of its chemical structure and similar compounds, long-term exposure or increase the risk of cancer, which seriously threatens human life and health.
    Therefore, for 2-pyridinonitrile, 5-nitro-3- (trifluoromethyl) substances, it is necessary to treat with caution and strengthen control to prevent them from causing serious harm to the environment and human health.