ethyl2-(2-(benzo[d]thiazole-2-sulfonamido)ethylamino)acetate

Looking at this "ethyl2-%282-%28benzo%5Bd%5Dthiazole-2-sulfonamido%29ethylamino%29acetate", it is actually a formula for the naming of organic chemistry. According to this name, in order to deduce its chemical structure, it is necessary to analyze the meaning of each part in detail.
"ethyl", ethyl is also an alkyl group containing two carbon atoms, expressed as "-C 2O H". "Acetate" means acetate or acetate, and its basic structure is "CH 🥰 COO-". These two are connected, and it can be seen that the compound contains the part of "CH 🥰 COOCH 🥰 CH 🥰".
Look again at "2-%282-%28benzo%5Bd%5Dthiazole - 2 - sulfonamido%29ethylamino". " benzo%5Bd%5Dthiazole ", benzo [d] thiazole is also a heterocyclic aromatic hydrocarbon containing sulfur and nitrogen, with the following basic skeleton: the benzene ring is fused with the thiazole ring, and the nitrogen and sulfur in the thiazole ring are at a specific position." 2-sulfonamido "indicates that there is a sulfonamide group connected to the 2-position of benzo [d] thiazole, that is," -SO 2O NH - "." 2-ethylamino "refers to the connection of ethylamino groups containing two carbons at the 2-position of the above structure, that is," -NHCH -2 CH ".
In summary, the chemical structure of this compound is: the 2-position of ethyl acetate is connected to a nitrogen atom through methylene, and the nitrogen atom is then connected to a 2- (benzo [d] thiazole-2 -sulfonamido) ethyl group. Its structure can be roughly described as: CH < unk > COOCH < unk > CH < unk > N (CH < unk > CH < unk > NHSO < unk > -benzo [d] thiazole), but more professional chemical drawing software is required for accurate drawing. This only describes its connection relationship in detail in text to clarify the approximate chemical structure.

Ethyl2 - (2 - (benzo [d] thiazole - 2 - sulfonamido) ethylamino) acetate is an organic compound with a wide range of uses.
In the field of medicine, this compound may have potential medicinal value. The Gain structure contains specific functional groups, such as benzothiazole and sulfonamide groups. Benzothiazole compounds often have a variety of biological activities, such as antibacterial, anti-inflammatory, and anti-tumor. Sulfonamide groups are also common in many drug molecules, or may participate in the interaction of drugs with biological targets, thereby regulating physiological processes. Therefore, ethyl2 - (2 - (benzo [d] thiazole - 2 - sulfonamido) ethylamino) acetate can be reasonably modified and modified to develop into new drugs for the treatment of specific diseases.
In the field of organic synthesis, it can be used as a key intermediate. With its own structural characteristics, it can couple with other compounds through various organic reactions, such as nucleophilic substitution, electrophilic substitution, etc., to construct more complex organic molecular structures. Therefore, synthetic chemists can use this compound as a starting material to design and synthesize organic materials with special functions and structures, such as natural product analogs, etc., to promote the development of organic synthetic chemistry.
In the field of materials science, or show unique properties. If it is introduced into polymer materials, it may endow the materials with new properties, such as improving the solubility, thermal stability, and mechanical properties of the materials. This compound may be used as a functional monomer to participate in the polymerization of polymers and prepare polymer materials with specific functions, which are used in coatings, plastics, fibers, and many other materials.

Ethyl2- (2- (benzo [d] thiazole-2-sulfonamido) ethylamino) acetate is an organic compound. Its physical properties are quite important and are related to the characteristics of many chemical applications.
The state of this compound is either solid at room temperature and pressure, but it also depends on factors such as the intermolecular force and melting point. If the intermolecular force is strong and the arrangement is orderly, it is solid; if the intermolecular force is weak, the arrangement is loose, or it is liquid.
The melting point is also a key physical property. The melting point is closely related to the molecular structure, such as the intermolecular hydrogen bond, the size of Van der Waals force, etc. If there are many and strong intermolecular hydrogen bonds, or if the van der Waals force is large, the melting point is relatively high; otherwise, it is relatively low. The melting point can be accurately determined experimentally, which is of great significance for its separation, purification and application.
The boiling point cannot be ignored either. The boiling point reflects the energy required for a compound to change from a liquid state to a gas state, and is related to the intermolecular force and relative molecular weight. The relative molecular mass is large, the intermolecular force is strong, and the boiling point is usually high. Boiling point information is extremely critical in separation operations such as distillation, which can help to effectively separate it from the mixture.
Solubility is also important. Its solubility in different solvents is different, and it has a certain solubility in organic solvents such as ethanol and acetone, or due to the principle of similar miscibility; while its solubility in water depends on the ratio and properties of hydrophilic groups and hydrophobic groups in its molecules. If it contains more hydrophilic groups or has a certain solubility in water, this property has far-reaching implications for drug development, chemical reaction solvent selection, etc.
In addition, density is also one of the physical properties. Density is related to the mass and volume of the compound. In practical applications such as mixing and separation of substances, density data can help to understand its distribution and behavior in the system. < Br >
The physical properties of this compound are diverse and interrelated, and are of great value in chemical research, industrial production and related application fields.

To prepare ethyl 2- (2- (benzo [d] thiazole-2-sulfonamido) ethylamino) acetate, the method is as follows:
Take benzo [d] thiazole first, and use an appropriate sulfonating agent, such as fuming sulfuric acid, at a suitable temperature and reaction time, sulfonate the 2-position of benzothiazole to obtain benzo [d] thiazole-2-sulfonic acid. Next, reagents such as thionyl chloride or phosphorus pentachloride are used to convert it into benzo [d] thiazole-2-sulfonyl chloride. This step of the reaction needs to be in an anhydrous environment, and suitable organic solvents such as dichloromethane can be selected to assist the solution. The reaction conditions also need to be carefully adjusted to ensure the yield. < Br > Take ethylenediamine and make one of the amino groups react with benzo [d] thiazole-2-sulfonyl chloride in a nucleophilic substitution reaction. In this reaction, an acid binding agent, such as triethylamine, can be used to absorb the hydrogen chloride generated by the reaction and promote the positive progress of the reaction. After the reaction, 2 - (benzo [d] thiazole-2 - sulfonamido) ethylamine is obtained.
Finally, 2 - (benzo [d] thiazole-2 - sulfonamido) ethylamine is reacted with ethyl chloroacetate in an alkaline environment, and potassium carbonate can be used as the base. The reaction is carried out in an organic solvent, such as N, N-dimethylformamide (DMF), through nucleophilic substitution to obtain ethyl 2- (2- (benzo [d] thiazole - 2 - sulfonamido) ethylamino) acetate. After the reaction, the product needs to be purified by extraction, column chromatography, etc. to obtain a high-purity target compound. The entire synthesis process, the conditions of each step of the reaction, such as temperature, reactant ratio, reaction time, etc., need to be carefully controlled to obtain satisfactory results.

Ethyl2- (2- (benzo [d] thiazole-2-sulfonamido) ethylamino) acetate is an organic compound. During use, all precautions must be clear.
First, safety protection is of paramount importance. This compound may be toxic and irritating. When operating, be sure to wear protective clothing, protective gloves and goggles to avoid skin contact and eye splashing. In case of inadvertent contact, rinse with plenty of water immediately and seek medical attention according to specific conditions.
Second, proper storage should not be ignored. Store in a cool, dry and well-ventilated place, away from fire sources and oxidants to prevent fire or chemical reactions. At the same time, store it separately from food, beverages, etc. to prevent the risk of ingestion.
Third, accurate operation is the basis for ensuring the smooth operation of the experiment or production. Before use, it is necessary to read the relevant information carefully and be familiar with its physical and chemical properties. When weighing and preparing the solution, it is necessary to operate accurately and follow the established procedures to ensure the reliability of the experimental data and the stability of the product quality.
Fourth, the disposal of waste must be carried out in accordance with regulations. Waste in the experiment or production process must not be discarded at will. It should be properly classified and disposed of in accordance with relevant environmental regulations to avoid pollution to the environment.
Fifth, ventilation conditions are indispensable. The operation should be carried out in the fume hood to ensure that the volatile gas can be discharged in time, reduce the concentration of harmful gases in the air, and protect the health of the operator.