(S)-2,3,5,6-Tetrahydro-6-phenylimidazo(2,1-b)thiazoletriylium phosphate

(S) -2,3,5,6-tetrahydro-6-benzylpurino (2,1-b) thiazole trivalent cationic lactate, which is a rather complex organic compound.
In terms of its physical properties, the morphology of the compound may vary depending on the preparation conditions and purity, and it is often presented as a crystalline solid. Looking at its color, it may be white to off-white, due to the arrangement of atoms and chemical bonds in the molecular structure, which absorbs and reflects light.
Melting point is also one of the important physical properties. However, its exact melting point value will be determined by factors such as lattice energy and intermolecular forces. The lattice energy comes from the electrostatic attractive force between ions, and the intermolecular forces include van der Waals force, hydrogen bonds, etc. In this compound, the interaction between atoms is complex, or a specific crystal structure is formed, and the melting point is in a specific range.
Solubility is related to its dispersion in different solvents. In water, because lactate is partially hydrophilic, or has a certain solubility, it can be associated with water molecules by hydrogen bonds; in organic solvents, such as ethanol and acetone, the solubility may vary depending on the overall polarity of the molecule and the interaction with the solvent molecules. Solvents with similar polarity may make the compound more soluble. Due to the principle of "similar miscibility", the intermolecular force is conducive to the dispersion of solutes in solvents.
In addition, the density of the compound is also determined by the degree of accumulation of molecular weight and crystal structure. If the molecular weight is large and the crystal structure is closely arranged, the density is relatively high.
The physical properties of this compound have a profound impact on its application in scientific research, medicine and other fields. For example, in drug development, solubility and melting point affect the way of drug preparation and the absorption and metabolism process in vivo; color and morphology are related to the appearance quality and stability of drugs.

(S) -2,3,5,6-tetrahydro-6-benzylimidazolo (2,1-b) thiazole trivalent cationic lactate, which is an organic compound. Its chemical properties are unique and have the following numbers:
First, from the perspective of ionic characteristics, this compound contains trivalent cations, which give it a certain charge property. The cation part can interact with negatively charged particles or groups electrostatically due to the action of charge. In solution, it can combine with anions to form ion pairs, which affects its solubility and stability. For example, in polar solvents, the interaction between cations and solvent molecules can increase the solubility of the compound.
Secondly, the lactate part also has important chemical properties. The lactate ion contains a carboxyl group, which makes it acidic to a certain extent. Although lactic acid is a weak acid, the carboxyl group can be dissociated under specific conditions, releasing hydrogen ions and participating in acid-base reactions. At the same time, the presence of lactate ions also affects the balance of hydrophilicity and hydrophobicity of the whole compound.
Furthermore, the imidazolo-thiazole structure and benzyl part in the molecule endow the compound with a specific spatial configuration and electron cloud distribution. The imidazolo-thiazole structure has a certain aromaticity, which makes it exhibit unique electronic effects and stereochemical characteristics in chemical reactions. The presence of benzyl increases the hydrophobicity and steric hindrance of the molecule. For example, benzyl groups can affect the interaction mode of compounds with other molecules. In some organic reactions, due to its steric hindrance, it will have an effect on the selectivity of the reaction, causing the reaction to prefer a specific path and produce products of a specific configuration.
The unique chemical properties of this compound may lead to applications in organic synthesis, medicinal chemistry and other fields. Its ionic properties, acidic groups and special structures lay the foundation for its participation in various chemical reactions and interactions.

The common route of (S) -2,3,5,6-tetrahydro-6-benzylpurino (2,1-b) thiazole trivalent cationic lactate is just like what Tiangong Kaiwu said, and it follows the ancient method.
To obtain this compound, one of the methods is to start with the raw material. Choose a suitable nitrogen-containing heterocyclic compound, such as a purine substrate, which has a reactive check point, just like a good material in front of the craftsman. React with benzylating reagents, benzyl can be cleverly connected to the sixth position of purine. This step requires precise control of the reaction conditions, such as temperature, solvent, and catalyst. It is like controlling the temperature and the utensil to make the benzyl just like the mortise and tenon. < Br >
After the benzyl group is introduced, the tetrahydrogenation is carried out. Often by catalytic hydrogenation, a suitable catalyst, such as palladium carbon, is selected, and the double bond of the purine ring is hydrogenated at a suitable pressure and temperature to achieve the tetrahydro structure. This process is like shaping the shape of an object and is carefully carved.
Then, the key thiazole ring formation step. With a sulfur-containing reagent and an appropriate nitrogen-containing compound, the thiazole ring is constructed through a condensation reaction to form the core structure of purine-thiazole. This reaction also needs to be carefully regulated to ensure that the reaction travels in the desired direction, like a craftsman carefully splicing parts.
As for the formation of trivalent cationic lactate, when the main structure of the compound is complete, it reacts with lactic acid under suitable conditions to protonate the compound to form a trivalent cation, and then binds with lactate to obtain the target (S) -2,3,5,6-tetrahydro-6-benzylpurino (2,1-b) thiazole trivalent cationic lactate. This is the state of success, such as the utensils are finally good. Every step needs to be handled carefully and follow ancient methods and chemical principles to obtain this compound.

To prepare (S) -2,3,5,6-tetrahydro-6-benzylpurino (2,1-b) thiazole trivalent cationic lactate, the method is as follows:
First take an appropriate amount of starting materials, through delicate reaction steps. For example, a substrate with a specific configuration is used in a suitable reaction environment, accompanied by appropriate reagents and conditions. Or the substrate is substituted first, and a specific functional group is ingeniously introduced. This step requires attention to the selectivity and yield of the reaction.
Then, with the help of cyclization, the core skeleton of purine-thiazole is carefully constructed. In this process, factors such as temperature and the amount of catalyst are all related to the success or failure of the reaction and the configuration of the product. Precise regulation is required to make the reaction proceed in the expected direction and obtain the ideal cyclization product.
Wait until the structure of purinothiazole is initially formed, then modify it, and introduce benzyl at a suitable check point. The reaction path and conditions need to be carefully selected to ensure that the position of benzyl introduction is accurate.
Finally, the resulting product is converted into a trivalent cationic lactate. In this step, a suitable salt-forming reagent and reaction environment need to be selected to make the product salt smoothly and ensure the purity and stability of the product.
The entire synthesis process is like a delicate chemical dance, with each step of the reaction interlocking. The control of the reaction conditions and the selection of reagents need to be as precise and meticulous as ancient craftsmen in order to obtain this target product.

(S) -2,3,5,6-tetrahydro-6-benzylimidazolo (2,1-b) thiazole trivalent cationic lactate during storage and transportation, pay attention to the following things:
First, this compound is quite sensitive to temperature and humidity. High temperature can easily cause its chemical structure to change, or lose its inherent activity; high humidity can also cause deliquescence and other conditions, which will damage its quality. Therefore, when storing, it is advisable to choose a cool and dry place, the temperature should be controlled within a specific range, and the humidity should also be maintained in a suitable range.
Second, because of its specific chemical activity, it cannot be stored and transported with strong oxidizing agents, strong reducing agents and substances with strong acidity and alkalinity. In contact with these substances, it is easy to induce chemical reactions, or cause explosions, fires and other hazards. When transporting, it should also be isolated from the above substances to ensure safe transportation.
Third, the packaging of this compound must be intact during storage and transportation. Damage to the packaging can easily cause it to leak, which will not only damage its own quality, but if it leaks into the environment or causes pollution to the environment, and if it comes into accidental contact with other substances, it may also cause unpredictable reactions. Therefore, it is extremely important to regularly check the integrity of the packaging.
Fourth, the handling process should be handled with care. Rough handling or damage to the packaging, and this compound may undergo unstable changes due to strong vibration and impact. Operators should also wear appropriate protective equipment to prevent accidental contact from causing harm to the body.