2-MERCAPTOBENZOTHIAZOLYL(Z)-2-AMINOTHIAZOLE-4-YL-2-METHOXY IMINO ACETATE

2-Mercaptobenzothiazolyl (Z) - 2-aminothiazole-4-yl-2-methoxyiminoacetate has a wide range of main uses. In the field of pharmaceutical and chemical industry, it is often an important intermediate.
This compound is very useful in the creation of new antibacterial drugs. Due to its unique structure, it can introduce other functional groups by means of organic synthesis, and then construct new compounds with high antibacterial activity. It may be used by doctors to deal with various bacterial infections and treat diseases.
In the field of pesticides, it also has its own uses. It can be chemically modified to produce pesticides with insecticidal and bactericidal effects. It can protect crops from pests and diseases, ensure abundant grain, and help agriculture flourish.
Furthermore, in the field of materials science, this compound may be able to participate in the preparation of special materials. After special processing, or endowing the material with unique properties, such as excellent oxidation resistance, stability, etc., the material is suitable for various special scenarios, such as aerospace, electronic equipment, etc., to promote the progress of science and technology. In conclusion, 2-mercaptobenzothiazolyl (Z) -2-aminothiazole-4-yl-2-methoxyiminoacetate is of great value in medicine, pesticides, materials, and many other fields, providing strong support for the development of various fields.

2-Mercaptobenzothiazolyl (Z) - 2-aminothiazole-4-yl-2-methoxyiminoacetic acid ester, this is an organic compound. Its physical properties are rich and diverse, and it is of great significance to the fields of chemistry and pharmacy.
Looking at its properties, under normal temperature and pressure, it is mostly solid or crystalline powder. Its color is usually white to light yellow, and its appearance is pure, without variegation or foreign matter. This is due to the regular molecular structure, good crystal form, and uniform light reflection.
When it comes to the melting point, the melting point of this compound is quite high, reaching about [X] ° C. Because of the strong intermolecular force, there are hydrogen bonds, van der Waals forces and other synergistic effects, high energy is required to destroy the lattice and cause it to melt.
In terms of solubility, it has a certain solubility in common organic solvents such as ethanol and acetone. This is because the molecule contains polar groups, which are similar to the polarity of organic solvents, and dissolve according to the principle of "similar miscibility". However, the solubility in water is very small, because its hydrophobic groups account for a large proportion, and the force of interaction with water molecules is weak.
The density is about [X] g/cm ³, the relative density is moderate, and it is slightly heavier than water. This is due to the combination of the type and quantity of atoms in the molecule, resulting in the mass distribution in the unit volume.
Furthermore, this compound has good stability and can be stored for a long time without decomposition under conventional conditions. However, under extreme conditions such as strong acid, strong base or high temperature, the molecular structure may be damaged, and chemical reactions occur, resulting in changes in properties.
In summary, the physical properties of 2-mercaptobenzothiazolyl (Z) -2-aminothiazole-4-yl-2-methoxyiminoacetic acid ester lay the foundation for its application in various fields, helping researchers to use it rationally according to its characteristics and maximize its value.

2-Mercaptobenzothiazolyl (Z) -2-aminothiazole-4-yl-2-methoxyiminoacetate is an organic compound with rich and diverse chemical properties.
Let's talk about solubility first. Because its molecular structure contains both polar groups such as amino groups, carboxyl ester groups, and non-polar benzene rings, it has a certain solubility in polar organic solvents such as methanol and ethanol, but relatively limited solubility in water. Polar solvents and polar groups of the compound can form hydrogen bonds and other interactions to help them dissolve. In terms of stability, the thiazole ring and benzothiazole ring of the compound are relatively stable. However, the thiol group has strong reductivity and is easily oxidized by oxidants such as oxygen in the air to form oxidation products such as disulfide bonds. And under acidic or basic conditions, its ester groups may undergo hydrolysis. Under acidic conditions, ester groups are hydrolyzed through protonated intermediates to gradually generate carboxylic acids and alcohols; under basic conditions, hydroxide attacks ester carbonyl carbons, and the hydrolysis rate is usually faster, resulting in carboxylic salts and alcohols. In the
reaction activity, the amino group can undergo nucleophilic substitution reaction, react with acyl halide, acid anhydride and other to form amide compounds; the thiol group can coordinate with metal ions to form stable complexes, which has potential applications in analytical chemistry and materials science. The double bond of the methoxyimino part can participate in addition reactions, such as Michael addition with nucleophiles.
The unique chemical properties of this compound make it show application potential in the fields of medicine and pesticides. In the field of medicine, its structure modification can be used to develop antibacterial and antiviral drugs; in the field of pesticides, high-efficiency and low-toxicity insecticides, fungicides, etc. can be developed based on its structure.

The production process of 2-mercaptobenzothiazolyl (Z) - 2-aminothiazole-4-yl-2-methoxyiminoacetate is an important matter in chemical synthesis. The synthesis process of this compound is similar to the ancient method of alchemy, and requires delicate proportions and appropriate heat.
The starting material is selected from 2-aminothiazole-4-carboxylic acid as the base, just like the rare medicine, and its purity is crucial. First, 2-aminothiazole-4-carboxylic acid is reacted with appropriate halogenating reagents, such as halogenated sulfoxide or phosphorus halide. This step is like igniting the fire of a Dan furnace and causing it to undergo halogenation to generate 2-halogenated thiazole-4-carboxylic acid derivatives. This reaction needs to be carried out at a suitable temperature and in an inert gas environment to prevent the incorporation of impurities, just like alchemy needs to be isolated from external turbid gases.
Then, the obtained halogenated derivative meets 2-mercaptobenzothiazole in an alkaline environment, and the two seem to blend yin and yang, resulting in a nucleophilic substitution reaction. The choice of base, such as potassium carbonate or sodium carbonate, requires precise control of the dosage and reaction conditions in order to make the reaction go smoothly and the product is produced as expected.
As for the partial introduction of 2-methoxy imino, methoxy amine hydrochloride is often combined with a suitable condensing agent in a suitable solvent to fuse with the above reaction products. This process requires careful observation of the reaction process. Temperature and time are key, just like alchemy observing the temperature, so that the methoxy imino group is successfully connected to the molecule, and finally 2-mercaptobenzothiazolyl (Z) - 2-aminothiazole-4-yl-2-methoxy iminoacetate is obtained. After synthesis, it still needs to be separated and purified, such as extraction, recrystallization, etc., to remove its impurities and leave its essence to obtain a pure product.

2-MERCAPTOBENZOTHIAZOLYL (Z) -2-AMINOTHIAZOLE-4-YL-2-METHOXY+IMINO+ACETATE is a rather complex chemical substance. During use, there are many key precautions to keep in mind.
Bear the brunt of it, and safety protection should not be underestimated. This substance may be toxic and irritating. It is necessary to wear appropriate protective equipment, such as gloves, goggles and protective clothing, when operating, to avoid direct contact with the skin and eyes, and prevent inhalation of its dust or volatile gases, which may cause damage to the body.
Furthermore, precise control of the dosage is essential. The substance should be accurately measured according to specific experimental or production needs, in strict accordance with prescribed standards and procedures. Improper dosage, or cause an unbalanced reaction, fail to achieve the desired effect, or even cause accidents.
At the same time, the storage conditions should not be ignored. It should be stored in a dry, cool and well-ventilated place, away from fire, heat and oxidants. Improper storage or deterioration of substances will affect its performance and use effect.
In addition, the ventilation conditions of the use place must be good. Good ventilation can disperse harmful gases that may be generated in time, reduce its concentration in the air, and ensure the health and safety of operators.
During operation, close attention should also be paid to the reaction situation. Carefully observe changes in temperature, pressure, color, etc. If there is any abnormality, appropriate measures should be taken immediately to prevent danger.
And the remaining substances and waste after use must not be discarded at will. Special treatment should be carried out in accordance with relevant environmental regulations and regulations to avoid pollution to the environment.
In short, when using 2-MERCAPTOBENZOTHIAZOLYL (Z) -2-AMINOTHIAZOLE-4-YL-2-METHOXY+IMINO+ACETATE, we must adhere to a rigorous and scientific attitude and pay attention to every detail to ensure the safe and smooth operation.