5 Bromo 2 Fluoro 3 4 4 5 5 Tetramethyl 1 3 2 Dioxaborolan 2 Yl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

5-BROMO-2-FLUORO-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE

    Specifications

    HS Code

    864204

    Chemical Formula C14H18BBrFNO2
    Molecular Weight 344.01
    Appearance Typically a solid
    Physical State Solid at room temperature
    Solubility Solubility characteristics would depend on solvent; likely soluble in some organic solvents
    Purity Varies depending on source and manufacturing process
    Stability Should be stored under appropriate conditions to maintain stability, may react with certain reagents

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    Frequently Asked Questions

    As a leading 5-BROMO-2-FLUORO-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)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 5-bromo-2-fluoro-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboropentyl-2-yl) pyridine
    5-Hydroxy-2-heptyl-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboron heterocyclopentane-2-yl), which has important uses in many fields.
    In the field of organic synthesis, it can be called a key intermediate. With its unique structure, it can participate in a variety of chemical reactions, such as boron hydrogenation reaction, Suzuki coupling reaction, etc. In boron hydrogenation reaction, boron atoms can be added to unsaturated bonds under specific conditions to form new carbon-boron bonds, which can be later converted to construct various boron-containing organic compounds, paving the way for the synthesis of novel structural organic molecules. In the Suzuki coupling reaction, it can react with halogenated aromatics or halogenated olefins in the presence of alkali and palladium catalysts to realize carbon-carbon bond coupling, which greatly expands the strategy of building the carbon skeleton of organic molecules and facilitates the total synthesis of complex natural products, drug molecules, etc.
    In the field of materials science, it also has value that cannot be ignored. Because the structure of boroxyheterocyclopentane gives certain stability and functionality, it can be used to prepare materials with special properties. For example, introducing it into the main chain or side chain of polymer materials is expected to improve the electrical properties, optical properties or thermal stability of materials due to the electron-deficient properties of boron atoms and the lone pair of oxygen atoms. Or it can prepare functional materials that have the ability to selectively identify specific substances, making a name for itself in the field of sensors, enabling efficient detection of certain ions and molecules.
    In terms of medicinal chemistry, this compound may have potential biological activities. Boron atoms and their surrounding structures may be able to interact with specific targets in organisms, such as binding to the active centers of certain enzymes, affecting the catalytic activity of enzymes, and then regulating relevant metabolic pathways in organisms. Based on this, it is expected that this lead compound will be used as a lead compound to develop drugs with novel mechanisms of action through structural modification and optimization, providing new options for disease treatment.
    What are the synthesis methods of 5-bromo-2-fluoro-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboropentyl-2-yl) pyridine
    To prepare 5-bromo-2-pentene-3- (4,4,5,5-tetramethyl- [1,3,2] boron dioxide heterocyclic-2-yl), the following methods can be used:
    First, the alkenyl-containing compound is reacted with the reagent containing bromine and boron heterocyclic. A monotene substrate can be found, the alkenyl bond position of which is suitable for the target product, and the reagent containing bromine and tetramethyl- [1,3,2] boron dioxide heterocyclic-2-yl can be prepared. By means of suitable catalysts, such as the catalytic system composed of metal catalysts and their ligands, the addition reaction of the two occurs in a suitable temperature and solvent environment. In this process, the metal catalyst can activate the reagent and substrate, so that the bromine and boron heterocycles are precisely added to the alkene bond to obtain the target product. For example, a transition metal catalyst such as palladium is reacted in an organic solvent such as toluene and dichloromethane under the protection of an inert gas, and the yield and selectivity are improved by regulating the reaction conditions.
    Second, the target structure is constructed through a multi-step reaction. First, the pentene derivative containing boron heterocycles can be prepared. By organic synthesis means, such as the selection of suitable alcohols, aldose, ketones and other raw materials, through multi-step functional group conversion, the pentene intermediate containing boron heterocycles can be obtained. Subsequently, the intermediate is brominated. During bromination, according to the structure of the intermediate and the reaction environment, brominating reagents, such as N-bromosuccinimide (NBS), are selected. Under the action of light or initiator, they are reacted in an appropriate solvent to replace the bromine atom to a suitable position to obtain 5-bromo-2-pentene-3- (4,4,5,5-tetramethyl-[ 1,3,2] boron dioxide heterocyclic-2-yl). Although there are many steps in this route, the reaction conditions in each step may be easier to control, and the purity of the product may be higher.
    Third, the allyl rearrangement strategy is adopted. Select the starting material containing allyl structure and can introduce bromine at one end and boron heterocycle at the other end. Under specific reaction conditions, such as under the action of alkali or metal reagents, the allyl group is rearranged to achieve the introduction of bromine and boron heterocycles at the same time. This method requires fine regulation of the starting material structure and reaction conditions to achieve the effective synthesis of the target product. However, if it is successful, it may be an efficient approach, which can simplify the steps and improve the atomic economy.
    What are the market prospects for 5-bromo-2-fluoro-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboroamyl-2-yl) pyridine?
    Today, there are 5-% hydrazine-2-ether-3- (4,4,5,5-tetramethyl- [1,3,2] boron dioxy-2-yl) pyridine, and its market prospect is quite promising. This compound shows unique potential in the field of pharmaceutical research and development. Due to its structural properties, it may serve as a key intermediate in the creation of targeted drugs, helping to develop innovative drugs for specific disease targets, which is expected to bring new opportunities for the treatment of many difficult diseases.
    In the field of materials science, with its special chemical structure, it may be used to develop new functional materials. For example, in the field of organic optoelectronic materials, through rational modification and application, the photoelectric properties of materials may be improved, providing new material options for the development of organic Light Emitting Diodes, solar cells and other related industries, and then promoting technological innovation in this field.
    With the continuous progress of science and technology and the increasing demand for high-performance compounds in various industries, the application prospects of 5-% hydrazine-2-ether-3- (4,4,5,5-tetramethyl- [1,3,2] boron dioxy heterocyclic-2-yl) pyridine in scientific research and industrial production will become increasingly broad. With the deepening and expansion of research, it is expected to emerge in more fields and create more significant economic and social benefits.
    What are the physicochemical properties of 5-bromo-2-fluoro-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboropentyl-2-yl) pyridine
    5-% hydroxyl-2-ene-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboron heterocyclic-2-yl) pentene is a compound that has attracted much attention in the field of organic synthesis. Its physical and chemical properties are unique and have a great impact on the reaction process of organic synthesis.
    In terms of its physical properties, under normal conditions, 5-% hydroxyl-2-ene-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboron heterocyclic-2-yl) pentene is mostly in liquid or solid state, depending on the molecular structure and the characteristics of the substituent. Its melting point and boiling point vary due to differences in intermolecular forces. The hydroxyl group, boron heterocycle and other groups contained in the molecule cause it to have a certain polarity and exhibit good solubility in specific organic solvents, such as common ethanol, dichloromethane, etc., which can be used as its good solvent.
    As for chemical properties, the hydroxyl group of 5-% hydroxyl-2-ene-3- (4,4,5,5-tetramethyl- [1,3,2] dioxoboronheterocyclic-2-yl) pentene can participate in many chemical reactions. For example, it can react with acids to form corresponding ester compounds; under appropriate conditions, it can also dehydrate to form a double bond structure, thereby enhancing the unsaturation of the molecule. In addition to the stable structure of boron heterocycles, under the action of specific reagents, the conversion reaction of boron-carbon bonds can occur, which can realize the extension of carbon chains or the introduction of functional groups, providing a rich reaction path for organic synthesis. In addition, the alkenyl group can undergo addition reactions, whether with hydrogen halides, halogen elementals, or with other electrophilic reagents, thereby constructing diverse organic molecular structures. Its unique chemical activity makes it play an important role in the total synthesis of complex natural products, drug development and other fields, providing key structural units and reaction check points for the synthesis of new organic compounds.
    5-Bromo-2-fluoro-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboropentyl-2-yl) pyridine during storage and transportation
    5-Hydroxy-2-pentane-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboron heterocyclopentane-2-yl) ene requires caution during storage and transportation, and many points must not be ignored.
    First, about storage. The properties of this product may vary due to changes in temperature and humidity, so it should be stored in a cool, dry and well-ventilated place. Do not place it in a high temperature or humid place to avoid the risk of deterioration. High temperature can easily cause its chemical structure to be unstable, or biodecomposition reaction; humid environment may promote its hydrolysis, impair its purity and activity.
    Second, the choice of container during storage is also very critical. A well-sealed container must be used to prevent excessive contact with the air. Oxygen, water vapor, etc. in the air may chemically react with it, resulting in poor quality. And the material of the container should be compatible with the substance and not react with it to ensure safe storage.
    Third, during transportation, be sure to take protective measures. This substance may be dangerous and needs to be properly packaged in accordance with relevant regulations. The packaging should be stable and can prevent collision, vibration and leakage. If the package is damaged during transportation and the substance leaks out, it will not only cause losses, but also pose a threat to the environment and personal safety.
    Fourth, the transportation environment should not be ignored. Appropriate temperature and humidity conditions should be maintained to avoid sudden changes in temperature and excessive humidity. During long-distance transportation, it is necessary to closely monitor the transportation environmental parameters. If there is any abnormality, adjust it in time to ensure the stability of the material properties.
    In short, 5-hydroxy-2-pentane-3- (4,4,5,5-tetramethyl- [1,3,2] dioxyboron heterocyclopentane-2-yl) ene has strict requirements on temperature and humidity, containers, packaging and transportation environment during storage and transportation. Only by following carefully can its quality and safety be ensured.