5 Bromo 2 Isopropoxy 1 3 Thiazole
quinoline thiophene imidazole thiazole

5-Bromo-2-isopropoxy-1,3-thiazole

    Specifications

    HS Code

    868941

    Name 5-Bromo-2-isopropoxy-1,3-thiazole
    Chemical Formula C6H8BrNOS
    Molar Mass 222.103 g/mol

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    Frequently Asked Questions

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    What is the main use of 5-bromo-2-isopropoxy-1,3-thiazole?
    5-2-propoxy-1,3-dialkane is commonly used in the field of chemical synthesis. Its main uses are as follows:
    First, it is important for chemical synthesis. In the synthesis of polyrefined compounds, 5-2-propoxy-1,3-dialkane can be used as a starting material for chemical synthesis. Because its molecules contain specific functional groups, such as dialkyl, these functional groups can be reacted by various chemical reactions, such as substitution reactions, addition reactions, etc., to other molecules with specific functions. For example, in some synthetic processes, the inverse activity of the alkyl group can be used to generate the inverse activity of other compounds containing specific functional groups, thus forming a molecular skeleton with specific biological activity.
    Second, it is also useful in the field of materials. This compound can be used in the synthesis of polymeric materials. Due to its special properties, it can be polymerized or modified into polymers to give polymers a wide range of properties. For example, when it is introduced into the synthesis of polyester materials, the alkyl group can be used to reverse the polymerization of polyesters, and the propoxy group and dialkyl group may affect the crystalline properties, solubility, and mechanical properties of the material, etc., so that the polyester material exhibits better performance in terms of materials such as polymers and other materials.
    Third, it also has a value in fragrance synthesis. The special taste of 5-2-propoxy-1,3-dialkane or the taste of the resulting mixture can be used for fragrances with special fragrances. The functional groups in its molecules can be used for common reactions in fragrance synthesis, such as esterification reactions, to generate fragrance compounds with different fragrance characteristics, which are rich in fragrance.
    What are the synthesis methods of 5-bromo-2-isopropoxy-1,3-thiazole?
    To prepare 5-bromo-2-isopropoxy-1,3-xylene, the following ancient methods can be used.
    First, start with 1,3-xylene and make it react with bromine under specific conditions. 1,3-xylene can be placed in a reaction vessel, and bromine can be slowly introduced with iron powder or iron tribromide as a catalyst. In this reaction, bromine atoms will preferentially replace the hydrogen atoms of methyl ortho and para-sites on the benzene ring, and mainly obtain 2-bromo-1,3-xylene. This is because methyl is an ortho-and para-locator, which can increase the density of electron clouds in the ortho-and para-sites of the benzene ring, making it more susceptible to attack by electrophilic reagents.
    Then, the resulting 2-bromo-1,3-xylene is reacted with sodium isopropanol. 2-bromo-1,3-xylene is placed together with sodium isopropanol in a suitable solvent, such as anhydrous ethanol, and heated to reflux. The alkoxy anion in sodium isopropanol is strongly nucleophilic and will attack the carbon atom connected to the bromine atom in 2-bromo-1,3-xylene. The bromine ion leaves, and then 5-bromo-2-isopropoxy-1,3-xylene is obtained. This is a nucleophilic substitution reaction.
    Second, you can also start with isopropanol, and first react it with sodium metal to obtain sodium isopropanol. Take an appropriate amount of isopropanol in a drying reactor, add sodium metal cut into small pieces, the reaction is violent, and hydrogen escapes until the sodium metal is completely reacted, that is, an alcoholic solution of sodium isopropanol is obtained.
    At the same time, 1, 3-xylene and bromine are obtained by the aforementioned catalytic bromination method. Then this product is added to the alcohol solution of sodium isopropanol, heated and stirred, and through a nucleophilic substitution reaction, 5-bromo-2-isopropoxy-1,3-xylene can also be obtained. When operating, pay attention to the control of reaction conditions, and the solvent must be dry to prevent side reactions from occurring. And bromine is corrosive and volatile, so it should be used with caution and operated with good ventilation.
    What are the physical properties of 5-bromo-2-isopropoxy-1,3-thiazole?
    5-Bromo-2-isopropoxy-1,3-catechol is a kind of organic compound. Its physical properties are as follows:
    Under normal temperature, it is mostly white to light yellow crystalline powder, which is easy to identify and distinguish.
    When it comes to melting point, it is usually in a specific temperature range, about [X] ° C. As an important physical property of a substance, melting point is of great significance in the identification and purification of this compound. The purity geometry of the substance can be determined by accurately measuring the melting point.
    Another word is solubility, which shows a certain solubility in organic solvents. For example, in common organic solvents such as ethanol and acetone, it has good solubility. This property is extremely critical in organic synthesis reactions. Many reactions need to be carried out in a solution environment. Good solubility provides the possibility for the smooth progress of the reaction. In water, its solubility is relatively poor, which is closely related to the hydrophobicity of the molecular structure of the compound.
    In addition, its stability is also one of the important physical properties. Under conventional storage conditions, this compound is relatively stable. However, if exposed to high temperatures, strong light or contact with specific chemicals, chemical reactions may also occur, resulting in structural changes, which in turn affect its properties. The physical properties of this compound play an important role in the fields of organic synthesis, medicinal chemistry, etc. It is of great significance to deeply understand and make good use of these properties for research and application in related fields.
    What are the chemical properties of 5-bromo-2-isopropoxy-1,3-thiazole?
    5-Hydroxy-2-isopropoxy-1,3-dialkane, the chemical properties of this substance are as follows:
    Its molecular structure contains special functional groups, giving it unique properties. From the perspective of hydroxyl (-OH), it has a certain polarity and can participate in the formation of hydrogen bonds. Due to the strong electronegativity of oxygen atoms in hydroxyl groups, it attracts hydrogen atom electron clouds strongly, making hydrogen atoms partially positive and can form hydrogen bonds with molecules or groups containing electronegative atoms (such as oxygen, nitrogen, etc.). This property affects its solubility, and its solubility may be higher in polar solvents (such as water and alcohols), because it can interact with solvent molecules by hydrogen bonds. < Br >
    The isopropyl part is composed of isopropyl and oxygen atoms. Isopropyl is an alkyl group with a certain steric resistance, which affects the overall spatial configuration of the molecule and the distribution of electron clouds. The steric resistance restricts the proximity between molecules and affects the aggregation state and physical properties of substances, such as melting point and boiling point. At the same time, the oxygen atom connects the isopropyl group with the rest of the molecule, which changes the distribution of the electron cloud at this part, which has an effect on the molecular reactivity.
    The structure of the 1,3-dialkane ring is relatively stable, and the atoms in the ring are connected to each other by covalent bonds to form a closed system. This structure affects molecular stability and reactivity. In some reactions, it is not easy to open the ring due to its stability. However, if the conditions are suitable, such as specific catalysts, temperatures and pressures, the dialkane ring may undergo ring-opening reactions and participate in various organic synthesis and conversion.
    Overall, 5-hydroxyl-2-isopropoxy-1,3-dialkane contains hydroxyl groups, isopropoxy groups and dialkane rings, which make it have both polar, steric resistance and ring structure stability. It may have various applications and reactions in organic synthesis, materials science and other fields.
    What is the market price of 5-bromo-2-isopropoxy-1,3-thiazole?
    I have heard your inquiry about the market price of pentachlorodiisopropoxy-1,3-dialkane. This is a chemical used in organic synthesis, but its specific market value varies according to time, place, quality and supply and demand conditions.
    Looking at the present, if it is in the prosperous places of the Central Plains, the price per catty may be between 300 and 500 yuan. If it is in a remote place, or due to the cost of transshipment, the price may be slightly higher, and the change in supply and demand in the city also affects its price. If there are many people who want it, and there are few people who supply it, the price will increase; on the contrary, if the supply exceeds the demand, the price will decrease.
    And the quality of this chemical is also related to the price. The price of pure is high, and the price of miscellaneous is low. It is by those who buy this product, often observe its quality and measure its price, to get a good and cheap choice. The merchants in the city also adjust their prices according to the changes of time to meet the needs of the city. Therefore, if you want to know the exact price, you should go to the market in person, or consult people in the industry, to get it.