2 3 5 6 Tetrahydro 6 Phenylimidazo 2 1 B Thiazole Hydrochloride
quinoline thiophene imidazole thiazole

(-)-2,3,5,6-Tetrahydro-6-phenylimidazo[2,1-b]thiazole hydrochloride

    Specifications

    HS Code

    251879

    Chemical Formula C11H13ClN2S
    Molecular Weight 240.75
    Appearance Solid (usually white or off - white powder)
    Odor Typically odorless
    Solubility In Water Moderately soluble
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol
    Melting Point Specific value would require literature search
    Pka Data would need to be sourced from relevant chemical databases
    Stability Stable under normal storage conditions

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    General Information
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    Frequently Asked Questions

    As a leading (-)-2,3,5,6-Tetrahydro-6-phenylimidazo[2,1-b]thiazole hydrochloride 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 (±) -2,3,5,6-tetrahydro-6-phenylimidazolo [2,1-b] thiazole hydrochloride?
    (±) -2,3,5,6-tetrahydro-6-benzylpiperido [2,1-b] quinazolinone carboxylic acid ketone, the chemical structure of this compound is as follows:
    This compound is a complex organic structure with a core structure of piperido [2,1-b] quinazolinone. Among them, benzyl is connected at position 6, and there is a tetrahydro structure, indicating that some unsaturated bonds in the molecule are hydrogenated to form a saturated structure. In the structure, there are ketocarbonyl groups related to carboxyl groups. Carboxyl groups can participate in various chemical reactions, such as ester formation, salt formation reactions, etc. Ketocarbonyl groups have nucleophilic addition and other reactive activities. The substituents at different positions in its structure endow the compound with unique physical and chemical properties.
    In the field of organic synthesis, compounds with such structures are often used as key intermediates to construct more complex molecules with biological activities. Its unique structural characteristics have attracted much attention in pharmaceutical chemistry research, and may have potential pharmacological activities, such as affinity for some specific receptors, which in turn exhibit biological activities such as antibacterial, anti-inflammatory, and anti-tumor. In addition, the electronic and spatial effects of different substituents can affect the overall properties and reactivity of molecules, providing a variety of strategies for drug design and optimization.
    What are the physical properties of (±) -2,3,5,6-tetrahydro-6-phenylimidazolo [2,1-b] thiazole hydrochloride
    The physical properties of (±) -2,3,5,6-tetrahydro-6-benzylpiperido [2,1-b] quinazolinone are as follows:
    This compound is mostly in solid form at room temperature, which is due to its strong intermolecular force, which makes the molecular arrangement relatively tight and orderly. Its melting point is of great significance for identification and purification. It has been experimentally determined that the melting point is in a specific temperature range. This value provides a key basis for the identification of compounds, and the accurate determination of the melting point helps to judge its purity. The higher the purity, the closer the melting point to the theoretical value.
    In terms of solubility, it exhibits different solubility characteristics in common organic solvents. In polar organic solvents such as ethanol and acetone, by virtue of the interaction between molecules and solvents, it can have a certain solubility. This property is convenient for processing as a reactant or product in related chemical reactions, and can promote the reaction to proceed efficiently in a homogeneous system. However, in non-polar organic solvents such as n-hexane, the solubility is very small due to the difference in molecular polarity.
    The density of the compound is also one of the important physical properties. The density value reflects its mass per unit volume. It has guiding value for calculating the dosage in practical applications and controlling the proportion when mixed with other substances.
    In addition, its appearance is also worthy of attention, generally showing a specific color and crystal form. The color may be due to the presence of chromophore groups in the molecular structure, and the crystal form is closely related to the molecular arrangement. The regular crystal form implies the orderly arrangement of molecules in the lattice, which is of great significance for the study of its solid-state structure and properties.
    What is the main use of (±) -2,3,5,6-tetrahydro-6-phenylimidazolo [2,1-b] thiazole hydrochloride?
    What are the main uses of (±) -2,3,5,6-tetrahydro-6-benzylpiperido [2,1-b] quinazolinone?
    (This chemical substance is more complex, and it may be difficult to find a direct corresponding record in "Tiangong Kaiwu". However, it can be inferred according to the ancient process ideas and the use of drugs and materials.)
    In ancient China, the uses of various substances often involved in the fields of medicine and process materials. If this substance has special chemical and physical properties, it can be used in medicine. Ancient healers studied the herbs and stones to heal diseases with their characteristics. Suppose this substance has specific biological activities, or can be used to process medicinal pills to nourish the body and treat diseases. For example, ancient alchemists often used complex minerals and plants to synthesize medicinal pills, hoping to prolong life, cure diseases and save people.
    Furthermore, it can be used for craftsmanship. Ancient craftsmanship was exquisite, and many materials were specially treated for the manufacture of utensils. If this material can affect the texture, color and other characteristics of the material, or play a role in dyeing, ceramic glaze preparation, metal smelting aids, etc. For example, in the dyeing process, special substances can be used as mordants to help the color adhere to the fabric; when ceramics are fired, some ingredients can change the luster and texture of the glaze.
    Or it can be used in the military field. In ancient wars, special materials were required for the production of weapons and protective equipment. If this substance can enhance the hardness and toughness of the material, it can be used to build weapons and armor, and enhance the combat effectiveness of the army.
    Although this object is not confirmed in "Tiangong Kaiwu", according to the ancient wisdom of material exploration and utilization, it may show unique value in medicine, technology, military and other aspects, adding luster to ancient production and life.
    What are the synthesis methods of (±) -2,3,5,6-tetrahydro-6-phenylimidazolo [2,1-b] thiazole hydrochloride?
    The synthesis of (±) -2,3,5,6-tetradeuterium-6-benzylpenicillinic anhydride and [2,1-b] thiazolidine anhydride is quite complicated, but there are also many ways to be found.
    First, the key intermediate is constructed by multi-step reaction with common starting materials. First, a compound containing a specific functional group is taken, and under suitable reaction conditions, it undergoes nucleophilic substitution with another reagent, so that the molecular structure can be initially established. This reaction requires precise control of temperature, pH and the ratio of reactants. A slight difference in the pool will affect the yield and product purity. < Br >
    Then, the intermediate is functionally converted, and the structural characteristics of the target molecule are gradually shaped by oxidation, reduction and other reactions. During this period, the oxidizing agent and reducing agent used need to be carefully selected, and different reagents will lead to different reaction paths and product configurations.
    Furthermore, through cyclization reaction, the desired cyclic structure is formed. The key to this step is to choose the appropriate catalyst and reaction solvent to promote the smooth progress of the cyclic reaction in the molecule, so as to achieve the purpose of constructing the target acid anhydride structure.
    Another method can start from another type of raw material, first through condensation reaction, splice small molecule fragments to generate compounds with a certain carbohydrate length and functional group distribution. Subsequently, the molecular skeleton is skillfully adjusted by rearrangement reaction to meet the structural requirements of the target product. Then, through protection and deprotection strategies, specific functional groups are selectively modified and treated to avoid unnecessary changes in subsequent reactions. Finally, through dehydration reaction, the acid anhydride structure is formed in the molecule, and the desired product is obtained.
    Synthesis of such compounds requires careful control of each step of the reaction. Many factors are interrelated. Only with careful planning and careful operation can it be possible to synthesize (±) -2,3,5,6-tetradeuterium-6-benzylpenicillinic anhydride and [2,1-b] thiazolidine anhydride efficiently and with high purity.
    What is the safety of (±) -2,3,5,6-tetrahydro-6-phenylimidazolo [2,1-b] thiazole hydrochloride?
    (±) -2,3,5,6-tetrahydro-6-benzylpiperido [2,1-b] quinazolinone quinazolinone, how safe is this substance?
    I look at this question, it is related to the safety of (±) -2,3,5,6-tetrahydro-6-benzylpiperido [2,1-b] quinazolinone quinazolinone. This is a complex substance in the field of fine chemistry, and its safety needs to be considered in many ways.
    When discussing the safety of chemical substances, the first thing to consider is their chemical structure and properties. ( ±) -2,3,5,6-tetrahydro-6-benzylpiperido [2,1-b] quinazolinone quinazolinone has a specific molecular structure, which may affect its stability and reactivity. If the structure is stable, it is not easy to decompose or react with other substances under normal conditions, and the safety is relatively high; if the structure is active, it is easy to participate in chemical reactions, or generate harmful substances, there is a potential safety hazard.
    Second, its toxicological characteristics need to be observed. When experimentally exploring its effects on organisms, such as acute toxicity, to see if the organism has symptoms of poisoning or even life-threatening when it is exposed to organisms in large doses for a short period of time; chronic toxicity should not be ignored, long-term low-dose exposure, or cause chronic diseases of organisms, such as organ damage, gene mutation, etc. It should also be considered for its mutagenicity. If it can induce genetic mutations in organisms, or cause genetic abnormalities in organisms, it is extremely harmful.
    Furthermore, its environmental safety is also the key. If this substance enters the environment, its degradability in the environment needs to be investigated. If it is easy to degrade into harmless substances, it has little impact on the environment; if it is difficult to degrade, it will remain in the environment for a long time, or it will be enriched through the food chain, endangering the
    However, based on the available information, it is difficult to determine the safety of (±) -2, 3,5,6-tetrahydro-6-benzylpiperazo [2,1-b] quinazolinone quinazolinone. Detailed experimental studies, comprehensive information on chemical properties, toxicological data and environmental behavior can be used to fully evaluate its safety.