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

DL-2,3,5,6-tetrahydro-6-benzylimidazolo [2,1-b] thiazolinone anhydride is an organic compound. Its chemical properties are particularly complex, and Rong Wu will explain it in detail.
Among this compound, it has a special ring structure, and the ring system of imidazolo [2,1-b] thiazolinone gives it unique chemical activity. The substituents on its ring, such as 2,3,5,6-tetrahydro and 6-benzyl moiety, have a great influence on its properties. The tetrahydro structure can increase the flexibility of its molecules, while the benzyl group introduces greater spatial resistance and aromaticity.
In terms of reactivity, the acid anhydride part is one of its active centers. Acid anhydrides are electrophilic and easily react with nucleophiles. Common ones, such as reacting with alcohols, can form ester compounds; reacting with amines, amide products can be obtained. This is because carbonyl carbons in acid anhydrides have high positive electricity and are vulnerable to attack by nucleophiles.
Furthermore, heteroatoms such as nitrogen and sulfur in their ring system also affect their chemical properties. Nitrogen atoms can participate in the formation of hydrogen bonds, which in turn affects the interactions between molecules. Sulfur atoms, on the other hand, can participate in some redox reactions or form coordination compounds with metal ions because they have lone pairs of electrons. The
DL configuration indicates that there are two enantiomers of this compound, and their physical and chemical properties may be different under certain conditions. In the fields of asymmetric synthesis or chiral recognition, the characteristics of this configuration may be of great significance.
In addition, the solubility of the compound is also related to its chemical structure. The molecule contains both a lipophilic benzyl moiety and a polar acid anhydride and ring system, so it may have good solubility in organic solvents such as dichloromethane and chloroform, but its solubility in water may be limited.
In summary, DL-2,3,5,6-tetrahydro-6-benzylimidazolo [2,1-b] thiazolinone anhydride exhibits diverse chemical properties due to its unique structure, which may have potential application value in organic synthesis, medicinal chemistry and other fields.

DL-2,3,5,6-tetrahydro-6-benzylpurino [2,1-b] thiazolidinone anhydride is a special organic compound, which is of great use in the fields of medicinal chemistry and organic synthesis.
In medicinal chemistry, this compound exhibits potential biological activity. First, it may have antiviral effect. The proliferation and spread of viruses depend on the action of many key proteins and enzymes, and the compound has a unique structure and can bind to virus-related proteins or enzymes to interfere with its normal function, thereby inhibiting virus replication. For example, in the study of some RNA viruses, the modified compounds can effectively reduce the viral titer, providing new opportunities for the development of antiviral drugs. Second, it also has potential in the field of anti-tumor. Tumor cells grow out of control, and their signaling pathways are very different from normal cells. This compound may target the unique signaling pathway nodes of tumor cells, block tumor cell proliferation signaling, and induce tumor cell apoptosis. Studies have shown that some derivatives exhibit significant inhibitory activity on specific tumor cell lines.
In the field of organic synthesis, DL-2,3,5,6-tetrahydro-6-benzylpurino [2,1-b] thiazolidinone anhydride is often used as a key intermediate. Because its molecular structure contains special structural units such as purines and thiazolidinones, it can be modified and expanded by various organic reactions. For example, the activity of its anhydride group can be used to react with nucleophiles such as alcohols and amines to build compounds with more complex structures. At the same time, benzyl and tetrahydrogens can be further derived through halogenation, oxidation and other reactions, laying the foundation for the synthesis of new organic functional materials or bioactive molecules. In the synthesis routes of many novel drug molecules and organic functional materials, this compound can be seen as an important intermediate, promoting the continuous development of organic synthesis chemistry.

To prepare DL-2,3,5,6-tetradeuterium-6-benzylpurine and [2,1-b] thiazole-4-carboxylic acid, the method is as follows:
First take suitable starting materials, preferably those with relevant functional groups, such as substances containing purine structure and thiazole ring that can be derived. Use ancient phases, or modify the purine ring part first, so that deuterium atoms can be introduced at specific positions. Deuterium atoms can be gradually introduced at positions 2, 3, 5, and 6 by means of special deuterium substitution reagents, such as deuterated halides or deuterium-containing acid bases, according to the reaction mechanism such as nucleophilic substitution or addition. This process requires attention to the precise regulation of the reaction conditions. Temperature, pH and reaction time are all critical to ensure that deuterium atoms are selectively accessed and do not overreact to cause by-products to clump.
After the tetradeuterium substitution of the purine ring is completed, the thiazolo ring structure can be constructed instead. Sulfur-containing reagents and suitable carbonyl compounds or halides can be used for condensation and cyclization. In the meantime, the introduction of benzyl also requires ingenuity. Or before cyclization, the raw material is brought with benzyl, and the benzyl is connected to a suitable check point by means of nucleophilic substitution; or after cyclization, the benzyl is connected to 6 bits by a specific reaction. In this reaction, when a catalyst is required, the type and dosage should be carefully selected to promote the efficient progress of the reaction and ensure the purity of the product.
After the reaction is completed, the separation and purification of the product should not be underestimated. According to the physical properties of the product and impurities, such as solubility, boiling point, polarity, etc., recrystallization, column chromatography and other methods can be selected. During recrystallization, find a suitable solvent to make the product dissolve when hot and precipitate when cold; column chromatography selects the appropriate fixed phase and mobile phase according to the principle of adsorption and elution to obtain a pure DL-2,3,5,6-tetradeuterium-6-benzylpurino [2,1-b] thiazole-4-carboxylic acid product. The entire synthesis process requires careful steps in accordance with chemical principles to achieve this target compound.

I have not heard of the market price of "DL-2,3,5,6-tetrahydro-6-benzylimidazolo [2,1-b] thiazolinone". This is a very specialized and specific chemical substance, and its price often varies depending on purity, yield, supply and demand.
If you want to know its exact price, you should consult a company specializing in chemical reagents, or a supplier of chemical raw materials. It may be useful in chemical, pharmaceutical research and development and other fields, but it is rare in the market, so it is difficult to say its price.
There may be a platform for chemical trading, or you can find information on its relevant price; or you can consult with scientific research institutions and chemical industry practitioners, who may know its approximate price due to business involvement. However, due to the constantly changing chemical market and the strong professionalism of this substance, in order to obtain an accurate price, real-time consultation must prevail.

DL-2,3,5,6-tetramethylimidazolium [2,1-b] thiazole carboxylic anhydride is a chemical compound. Its safety is of paramount importance and should not be neglected.
As far as toxicity is concerned, this compound may be toxic to a certain extent and can cause adverse effects on organisms. If it is accidentally inhaled, skin-to-skin or food into the human body, it may cause pain, heart attack, vomiting and other diseases, which may endanger life. Therefore, during operation, preventive measures must be taken and must not be taken.
Its chemical properties also need special attention. Under specific conditions, or other chemical substances can be reactive, and toxic or flammable and explosive substances can be released. Therefore, it is necessary to store the incompatible materials separately, and properly control the degree, degree, and transparency of the environment to prevent accidental generation.
Furthermore, the behavior of this object in the environment cannot be ignored. Once it enters the environment, or the water, soil and air pollution are caused, it will disrupt the balance of life and affect the biodiversity of biology. Therefore, during the use of the equipment, the equipment must follow the relevant safety regulations and discharge.
Operating DL-2,3,5,6-tetramethylmethylimidazolium [2,1-b] thiazole carboxylic anhydride, workers need to wear protective clothing, gloves and eyes, and must wear respiratory protection equipment. After the operation, it is necessary to wash the clothes as soon as possible. If there is an accidental leakage, it will immediately cause an emergency case, quickly isolate the leakage pollution, restrict the entry and exit of people, and clean up and place it by people. In addition, only by paying attention to its safety in an all-round way and complying with all procedures can we effectively avoid the accident and ensure the safety of the human environment.