2 Cyanopyridine 3 Boronic Acid
pyridine pyrrole pyrazine piperidine piperazine

2-Cyanopyridine-3-boronic acid

    Specifications

    HS Code

    791312

    Chemical Formula C6H5BN2O2
    Molecular Weight 146.92 g/mol
    Appearance White to off - white solid
    Cas Number 1256355-23-0
    Melting Point 125 - 129 °C
    Solubility In Water Moderate
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, ethanol
    Pka Value ~8.5 (approximate value for boronic acid group)
    Stability Stable under normal conditions, but sensitive to moisture
    Boiling Point Decomposes before boiling

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    Frequently Asked Questions

    As a leading 2-Cyanopyridine-3-boronic acid 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 2-Cyanopyridine-3-boronic acid?
    2-Cyanopyridine-3-boronic acid is an important reagent in organic synthesis. It has many unique chemical properties and has a profound impact on the process of organic synthesis.
    In terms of its acidity, boric acid partially contains hydroxyl groups, which can give protons under specific conditions and exhibit a certain acidity. However, its acidity is weaker than that of common inorganic acids. This acidic property can be used as a mild acidic catalyst in many organic reactions to help the reaction progress smoothly. For example, some condensation reactions, esterification reactions, etc., it can speed up the reaction rate and improve the reaction efficiency by providing a moderately acidic environment.
    Furthermore, the presence of cyanyl groups endows the compound with unique reactivity. The cyanyl group is a strong electron-absorbing group, which can reduce the electron cloud density on the pyridine ring, making the pyridine ring more vulnerable to electrophilic attack. At the same time, the cyanyl group itself can also participate in many reactions, such as hydrolysis reaction can be converted into carboxyl group, reduction reaction can be changed to amino group, etc., which greatly expands the reaction path and derivation possibility of the compound.
    From the perspective of spatial structure, the planar structure of the pyridine ring and the spatial distribution of boric acid and cyano groups determine the stereochemical properties of its molecules. This spatial structure factor plays a key role in the process of molecular recognition and interaction with other molecules. For example, in some coordination reactions or supramolecular assembly processes, its unique spatial structure can precisely match specific receptors to achieve specific functions.
    In addition, the stability of 2-cyanopyridine-3-boronic acid also affects its chemical properties to a certain extent. Under normal temperature and pressure and conventional storage conditions, the compound is relatively stable. In case of extreme conditions such as high temperature, strong acid, and strong base, its structure may change, triggering various chemical reactions.
    2-cyanopyridine-3-boronic acid occupies an important position in the field of organic synthesis chemistry due to its acidity, cyano activity, spatial structure and stability. It provides a rich strategy and approach for the synthesis of many complex organic compounds.
    What are the main uses of 2-Cyanopyridine-3-boronic acid?
    2-Cyanopyridine-3-boronic acid, an important reagent in organic synthesis, is widely used in many fields.
    First, in the field of medicinal chemistry, it is often a key intermediate. Drug development is dedicated to creating compounds with specific biological activities. 2-cyanopyridine-3-boronic acid can be coupled with other organic molecules to build complex drug molecular structures. For example, in the synthesis process of many anti-tumor drugs, using this as a raw material, through clever reaction design, specific functional groups are introduced, giving the drug the ability to precisely target tumor cells, and helping to improve the stability and bioavailability of the drug.
    Second, it is also of great value in the field of materials science. With the increase in demand for advanced materials, it can participate in the preparation of functional materials. For example, when preparing photoelectric materials, 2-cyanopyridine-3-boric acid participates in the reaction, which can regulate the electronic structure and optical properties of the material, so that the material exhibits excellent performance in Light Emitting Diode, solar cells and other devices, such as improving photoelectric conversion efficiency.
    Furthermore, in the methodological research of organic synthesis chemistry, it is a commonly used substrate. Chemists use this to explore novel reaction pathways and catalytic systems to expand the boundaries of organic synthesis. Such as exploring new transition metal catalyzed reactions, the special structure of 2-cyanopyridine-3-boronic acid can provide a unique reaction check point, help to discover efficient and green synthesis methods, promote the development of organic synthesis chemistry, and provide new strategies for the construction of more complex organic molecules.
    What are the synthetic methods of 2-Cyanopyridine-3-boronic acid?
    The synthesis method of 2-cyanopyridine-3-boronic acid is an important topic in the field of organic synthesis. Common synthesis routes include the reaction of boron-containing reagents with pyridine derivatives.
    First, it can be prepared by the cross-coupling reaction of halogenated pyridinonitrile and organoboron reagents catalyzed by metal catalysts such as palladium. This reaction condition needs to be precisely regulated. The halogen atom activity of halogenated pyridinitrile and the structure of organoboron reagents have a great influence on the reaction. The type and dosage of bases in the reaction system, and the polarity of solvents are also key factors. Appropriate bases can promote the reaction, and suitable solvents can improve the solubility and reactivity of reactants.
    Second, using pyridine-3-boronic acid as the starting material, the target product can also be obtained by cyanylation reaction. In this process, the selection of cyanylation reagents is very important, and the reaction activity and selectivity of different cyanylation reagents are different. The reaction temperature, time and other conditions also need to be carefully optimized to achieve the best yield and purity.
    Furthermore, with the help of the functional group conversion strategy of pyridine derivatives. Introduce convertible groups at specific positions of pyridine first, and then gradually construct cyano and boric acid groups through a series of reactions. This method requires strict control of the intermediates in each step to ensure the reaction direction and product purity. < Br >
    Synthesis of 2-cyanopyridine-3-boronic acid requires comprehensive consideration of various reaction conditions and raw material characteristics, and repeated optimization can achieve high-efficiency and high-purity synthesis.
    What to pay attention to when storing and transporting 2-Cyanopyridine-3-boronic acid
    2-Cyanopyridine-3-boronic acid is a chemical substance. When storing and transporting, there are several matters that need to be paid attention to.
    This substance should be stored in a dry, cool and well-ventilated place. Because of its certain chemical activity, it is afraid of adverse reactions when exposed to moisture or high temperature. Moisture can easily cause its hydrolysis, and high temperature may cause decomposition, which will damage its quality and purity. Therefore, when storing, it is necessary to keep the environment dry and cool, and it can be placed next to the desiccant to avoid the risk of moisture.
    When transporting, caution is also required. Packaging must be tight to prevent leakage. If the package is damaged, the substance may interact with the external environment, which will damage itself or endanger the surrounding area. And the transportation process should avoid vibration and collision, because of its stability or affected by such external forces.
    Furthermore, this substance may have certain toxicity and irritation. Storage and transportation personnel, in front of appropriate protective equipment, such as gloves, goggles, etc., to prevent contact injury. If inadvertent contact, rinse with plenty of water quickly, and seek medical treatment according to the severity of the injury.
    In general, the storage and transportation of 2-cyanopyridine-3-boronic acid requires attention to the environment, packaging and personnel protection to ensure its quality and safety and avoid accidents.
    What is the market price range for 2-Cyanopyridine-3-boronic acid?
    2-Cyanopyridine-3-boronic acid, the price of this product fluctuates in the market, due to various reasons. Looking at the market conditions in the past, its price often varies depending on the price of raw materials, the complexity of the process, and the situation of demand.
    If the raw materials are abundant and cheap, the preparation method is simple, and when the supply exceeds the demand, the price may decrease. On the contrary, raw materials are scarce, the process is complicated, and the demand exceeds the supply, and the price will rise.
    Past records show that the price per gram may range from tens of yuan to hundreds of yuan. However, the market situation is unpredictable and it is difficult to determine the value. If there is no big difference in recent times, the price per gram may be around 100 yuan. This is just speculation, and the actual price must be consulted with various chemical material suppliers to be sure. Because the chemical industry market is changing rapidly, the opening of new sources, the issuance of new regulations, and the change of times can all cause changes in prices. Therefore, in order to get accurate prices, the current question is the way to go.