6 Phenyl 2 3 5 6 Tetrahydroimidazo 2 1 B 1 3 Thiazole Hydrochloride 1 1
quinoline thiophene imidazole thiazole

6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole hydrochloride (1:1)

    Specifications

    HS Code

    518561

    Chemical Name 6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole hydrochloride (1:1)
    Molecular Formula C11H13ClN2S
    Molecular Weight 240.757 g/mol
    Appearance Typically a solid (appearance may vary based on purity and preparation)
    Melting Point Data specific to this compound needed (varies by sample purity etc.)
    Solubility Solubility characteristics depend on solvent; may be soluble in some organic solvents and water to certain extents
    Pka Data specific to this compound needed
    Logp Data specific to this compound needed
    Stability Stability can be affected by factors like temperature, light, and humidity

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    General Information
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    Frequently Asked Questions

    As a leading 6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b][1,3]thiazole hydrochloride (1:1) 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 chemical structure of 6-phenyl-2,3,5,6-tetrahydroimidazo [2,1-b] [1,3] thiazole hydrochloride (1:1)?
    Alas! The chemical structure of this "6-phenyl-2,3,5,6-tetrahydroimidazo [2,1-b] [1,3] thiazole hydrochloride (1:1) " is quite exquisite. Looking at its name, "6-phenyl" shows that benzene is based on a 6-position, benzene ring, a six-membered carbon ring, with aromatic properties. It is a common structural unit in organic chemistry. Its stable conjugate system affects the physical and chemical properties of molecules.
    Table 2, 3, 5, and 6 of "2,3,5,6-tetrahydro" shows a tetrahydro structure. The tetrahydro state makes this part different from the totally unsaturated structure, or the flexibility of the molecule increases, which affects its spatial conformation and reactivity.
    "imidazo [2,1-b] [1,3] thiazole" is a core heterocyclic structure composed of imidazole and thiazole. The imidazole ring contains dinitrogen atoms, which have certain basic and coordination capabilities; the thiazole ring contains nitrogen and sulfur atoms, which combine to form a unique electron cloud distribution and spatial configuration, endowing the molecule with diverse chemical activities. < Br >
    and "hydrochloride (1:1) " indicate that this compound forms a salt of hydrochloric acid in a ratio of 1:1. After salt formation, the physical properties such as solubility and stability of the compound may change significantly, which is crucial in practical applications, such as affecting its behavior in solution and bioavailability.
    Overall, this compound has a delicate structure and the interaction of various parts gives it unique chemical and physical properties, which may have potential application value in organic synthesis, drug development and other fields.
    What are the physical properties of 6-phenyl-2,3,5,6-tetrahydroimidazo [2,1-b] [1,3] thiazole hydrochloride (1:1)?
    6-Phenyl-2,3,5,6-tetrahydroimidazolo [2,1-b] [1,3] thiazole hydrochloride (1:1) is also an organic compound. Its physical properties are particularly important, related to its use and characteristics.
    First of all, its appearance is often powdery, white and delicate, just like the first snow in winter, pure and uniform, which is easy to observe and deal with. Looking at it, its particles are uniform, without obvious agglomerations or impurities, and under light, it is slightly glossy, showing a pure state.
    As for solubility, this compound has different manifestations in water and common organic solvents. In water, it has a certain solubility. Although it is not very soluble, it can be gradually dissolved by moderate stirring and heating, forming a clear solution, just like fine sand merging into a stream, quietly. In organic solvents such as ethanol and dichloromethane, the solubility is better, and it can be quickly dispersed and dissolved. For example, salt is added to soup, and there is no shadow in an instant. This characteristic makes it more convenient to select solvents in chemical synthesis and separation and purification steps.
    Its melting point is also a key physical property. After rigorous determination, the melting point of this compound is in a specific range, which is like a precise door that opens the journey of physical state transformation at a certain temperature. When heated to this temperature, its solid state gradually melts and turns into a flowing liquid phase. This temperature is constant and accurate, which is an important basis for identification and purity determination.
    In addition, the compound has a specific density, although intangible, it exists in a delicate relationship between mass and volume. When weighing and measuring, the ratio of its mass to the space occupied is constant, just like the inherent characteristics of objects, which is crucial for storage, transportation and preparation of precise dosage products.
    In summary, the physical properties of 6-phenyl-2,3,5,6-tetrahydroimidazo [2,1-b] [1,3] thiazole hydrochloride (1:1), such as appearance, solubility, melting point, density, etc., are the cornerstones of its function in the field of chemistry, providing a solid foundation for scientific research and industrial applications.
    What are the main uses of 6-phenyl-2,3,5,6-tetrahydroimidazo [2,1-b] [1,3] thiazole hydrochloride (1:1)?
    6-Phenyl-2,3,5,6-tetrahydroimidazolo [2,1-b] [1,3] thiazole hydrochloride (1:1), this is a rather special chemical substance. It has a wide range of uses and has important applications in many fields.
    In the field of pharmaceutical research and development, it is often used as a key intermediate. Physicians and pharmacists try to explore its potential in the treatment of diseases by studying its chemical structure and properties. Or it can be converted into specific pharmacologically active compounds by ingenious chemical modification to fight various diseases, such as bacterial infections, inflammatory reactions, and even may play a role in the treatment of certain chronic diseases.
    In the field of chemical synthesis, it is also an indispensable raw material. Chemical craftsmen use its unique chemical properties to integrate it into complex synthesis routes to prepare more diverse and unique organic compounds. These compounds may be applied in the field of materials science, such as the manufacture of polymer materials with special properties, used in electronic components, plastic products, etc., giving products unique characteristics such as excellent stability, conductivity or optical properties.
    Furthermore, in the path of scientific research, this substance provides an excellent research object for chemical researchers. Through in-depth investigation of its reaction mechanism and physicochemical properties, it can enhance the scientific community's understanding of related chemical fields, lay the foundation for the construction of new theories and the birth of new technologies, promote the continuous development of chemistry, and open up unknown scientific frontiers.
    What is the synthesis method of 6-phenyl-2,3,5,6-tetrahydroimidazo [2,1-b] [1,3] thiazole hydrochloride (1:1)?
    To prepare 6-phenyl-2,3,5,6-tetrahydroimidazolo [2,1-b] [1,3] thiazole hydrochloride (1:1), the method is as follows:
    First take appropriate starting materials, usually phenyl-containing compounds and thiazole-containing structural precursors. Place the two in a suitable reaction vessel, add an appropriate amount of solvent, such as ethanol, dichloromethane, etc., so that the raw materials can be fully dissolved and in contact with each other, which is conducive to the reaction.
    During the reaction, the temperature conditions need to be controlled. Depending on the reaction characteristics, either at room temperature or heated to a specific temperature, such as 50-80 degrees Celsius, to accelerate the reaction. At the same time, appropriate catalysts can be added to change the chemical reaction rate and make the reaction more efficient.
    When the reaction reaches the expected level, monitor the reaction process by thin-layer chromatography to confirm that the raw material conversion is complete or reaches an appropriate proportion, and then proceed to post-treatment. The reaction liquid is first cooled, and then the product is separated in a suitable way, such as extraction, filtration, etc. If the product contains impurities, a suitable solvent can be selected by recrystallization, such as a mixed solvent of ethyl acetate and petroleum ether, to purify to improve the purity of the product.
    Finally, the purified product is reacted with hydrochloric acid in a ratio of 1:1 to form 6-phenyl-2,3,5,6-tetrahydroimidazolo [2,1-b] [1,3] thiazole hydrochloride (1:1). After the reaction is completed, it is dried and other treatments to obtain the target product. The whole process needs to pay attention to the operating specifications to ensure safety, and pay attention to the details of each step to control, in order to obtain high-purity products.
    What are the safety precautions for 6-phenyl-2,3,5,6-tetrahydroimidazo [2,1-b] [1,3] thiazole hydrochloride (1:1)?
    6-Phenyl-2,3,5,6-tetrahydroimidazolo [2,1-b] [1,3] thiazole hydrochloride (1:1), this is a special chemical substance. When using, many safety precautions must be kept in mind.
    bear the brunt, this substance may be toxic. After exposure, it may cause damage to human health, such as skin allergies, skin itching, redness and swelling; if not carefully entered the eyes, it can cause severe eye pain and blurred vision. What's more, inhaling its dust, or causing respiratory discomfort, causing cough, asthma, long-term exposure, or even affecting lung function. Therefore, when operating, protective equipment is essential, and protective clothing is required, which can effectively block its contact with the skin; wear protective gloves to avoid hand contamination; wear protective glasses to protect the eyes; and wear a suitable respirator to prevent inhalation of dust.
    Furthermore, the substance is also particular about storage. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. Because of its flammability, it may encounter open flames, hot topics, or cause combustion, or even explosions, causing disaster. And it needs to be stored separately from oxidants, acids, etc. Because of its chemical properties, it is lively, mixed with these substances, or causes severe chemical reactions, endangering safety.
    In addition, the place of use must be well ventilated to reduce the concentration of this substance in the air. After the operation, be sure to wash the body and clothing thoroughly to remove any residues. If there is a substance spilled during the operation, do not panic, and clean it up immediately according to scientific methods to prevent its spread and cause greater harm. Only by paying attention everywhere and strictly following safety procedures can the operation be safe and protected from its harm.