4 Chloro 2 Oxo 3 2h Benzothiazoleaceticaci
quinoline thiophene imidazole thiazole

4-chloro-2-oxo-3(2h)-benzothiazoleaceticaci

Taiy Chemical

Specifications

HS Code

451862

Chemical Formula C9H6ClNO3S
Molar Mass 243.67 g/mol
Appearance Solid (usually white to off - white powder)
Melting Point Typically in a certain range (needs specific data, e.g., 180 - 185°C)
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO, DMF
Pka Specific pKa value relevant to its acidic group (data needed)
Density Requires specific experimental value
Stability Stable under normal conditions, may decompose on heating or in contact with strong oxidizing agents
Ir Spectrum Characteristics Characteristic absorption bands for carbonyl, aromatic, sulfur - containing, and chloro - groups
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General Information
Frequently Asked Questions
What are the chemical properties of 4-chloro-2-oxo-3 (2h) -benzothiazoleaceticaci
4-Chloro-2-oxo-3 (2H) -benzothiazole acetic acid, this material has unique properties and is one of the organic compounds with considerable research value.
Its physical properties are mostly solid at room temperature, white or nearly white, like a fine powder, uniform and delicate. Smell, there is little special odor emitted, but at high concentrations or under specific conditions, it may feel a slight odor. Its melting point is a specific value. At this temperature, the substance gradually melts from solid to liquid. This property can be used as an important basis for identification and purification.
In terms of chemical properties, the compound has significant reactivity. Because its structure contains active groups such as chlorine atoms, carbonyl groups and benzothiazole rings, it can initiate a variety of chemical reactions. For example, chlorine atoms can participate in nucleophilic substitution reactions, and under appropriate reagents and conditions, can be replaced by other nucleophilic groups, thereby deriving new compounds with richer structures. This is widely used in the field of organic synthesis. The existence of carbonyl groups allows them to participate in reactions such as condensation and addition, and can condensate with compounds containing active hydrogen to form new carbon-carbon or carbon-heteroatom bonds. The benzothiazole ring endows the molecule with certain aromaticity and stability, and also affects the selectivity of the reaction and the activity check point. In addition, the acetic acid structure can exhibit the typical properties of carboxylic acids, such as neutralization with bases to form salts, and esterification with alcohols to form esters. Such reactions are important synthesis paths in many fields such as pharmaceutical chemistry and materials science.
4-chloro-2-oxo-3 (2H) -benzothiazole acetic acid has rich chemical properties, providing many possibilities and opportunities for organic synthesis and related fields of research.
What are the physical properties of 4-chloro-2-oxo-3 (2h) -benzothiazoleaceticaci
4-Chloro-2-oxo-3 (2H) -benzothiazole acetic acid, this is an organic compound. Its physical properties are quite important, which is related to its application in many fields.
Looking at its properties, under normal temperature and pressure, 4-chloro-2-oxo-3 (2H) -benzothiazole acetic acid is often white to white crystalline powder. This form is easy to store and transport, and it is easy to handle in subsequent processing.
Talking about the melting point, the melting point of this compound is in a specific range, generally about [X] ° C. The determination of the melting point is crucial for the identification of its purity and the determination of its physical properties. The precise value of the melting point is the characteristic identification of the compound, which can help to distinguish it from other analogs.
Solubility is also one of the important physical properties. 4-chloro-2-oxo-3 (2H) -benzothiazole acetic acid exhibits different solubility in different solvents. In organic solvents such as ethanol and acetone, it has a certain solubility and can form a uniform solution. In water, its solubility is relatively low. This difference in solubility is of great significance in chemical synthesis, separation and purification, and preparation.
Furthermore, its density is also a specific value, about [X] g/cm ³. The density reflects the mass per unit volume of the substance, and the density data is indispensable for the measurement, mixing and process design of the compound.
In addition, the stability of 4-chloro-2-oxo-3 (2H) -benzothiazole acetic acid is also worthy of attention. Under normal storage conditions, its chemical properties are relatively stable, but under certain conditions such as high temperature, high humidity or light, decomposition or other chemical reactions may occur. Therefore, during storage and use, attention should be paid to suitable environmental conditions to ensure its quality and performance.
What is the common use of 4-chloro-2-oxo-3 (2h) -benzothiazoleaceticaci
4-Chloro-2-oxo-3 (2H) -benzothiazole acetic acid, an organic compound. In the field of chemical synthesis, its common uses are quite extensive.
First, in the field of pharmaceutical chemistry, this compound is often used as a key intermediate. Due to its unique structure, it can be chemically modified and transformed to derive many biologically active substances. For example, new drugs with antibacterial, anti-inflammatory or anti-tumor activities can be developed by modifying its benzothiazole ring and acetic acid side chain. Geiinbenzothiazole compounds themselves exhibit a variety of biological activities, and the specific substituents attached to this compound enrich the direction in which they can be derived.
Second, in the field of pesticide chemistry, it also plays an important role. It can be converted into pesticide components with efficient control effect on crop pests through a series of reactions. For example, pesticides based on this structure can effectively inhibit the growth and reproduction of specific pests, and have relatively little impact on the environment, in line with the current trend of green pesticide development.
Furthermore, in the field of materials science, 4-chloro-2-oxo-3 (2H) -benzothiazole acetic acid can also play a role. It can be used to combine or react with other materials to prepare functional materials with special properties. For example, it may improve the optical, electrical or mechanical properties of the material, thereby expanding the application range of the material.
In summary, 4-chloro-2-oxo-3 (2H) -benzothiazole acetic acid has a wide range of important uses in many fields such as medicine, pesticides and materials science due to its unique structure, providing a rich material basis and research direction for research and development in various fields.
What are the synthesis methods of 4-chloro-2-oxo-3 (2h) -benzothiazoleaceticaci
The synthesis method of 4-chloro-2-oxo-3 (2H) -benzothiazole acetic acid has been known for a long time. There are many methods, each with its own advantages.
One is to use benzothiazole as a group, introduce chlorine atoms at specific positions through chlorination, and then use an ingenious method to construct carbonyl groups at 2 positions, and then introduce acetic acid groups. This process requires careful study of the reaction conditions. The choice of temperature, solvent and catalyst is all about success or failure. If the temperature is too high, it may cause side reactions and lead to impure products; if the temperature is too low, the reaction will be slow and take a long time. The nature of the solvent is related to the dissolution and reactivity of the reactants. If it is not selected properly, the reaction will be difficult. The ability of the catalyst to accelerate the reaction process and increase the yield also needs to be adapted, otherwise it will be futile.
Second, or start from other sulfur-containing and nitrogen-containing heterocyclic compounds, and gradually build the target molecular structure through several steps of transformation. This approach requires a good understanding of heterocyclic chemistry, knowing the mechanism and conditions of each step of the reaction. Each step of transformation requires weighing the pros and cons, considering the difficulty of the reaction, the level of yield, and the number of side reactions. During this process, many organic reactions are involved, such as substitution, addition, oxidation, and reduction. Each reaction is interdependent and interconnected. If any link is wrong, it is difficult to achieve the goal.
Third, natural products are also used as starting materials and chemically modified to convert into 4-chloro-2-oxo-3 (2H) -benzothiazole acetic acid. This method takes advantage of the unique structure of natural products to reduce the synthesis steps, but the acquisition, separation and purification of natural products are also challenges. It is necessary to find abundant sources and master efficient separation techniques to ensure the quality and quantity of raw materials.
Although the road to synthesis is full of difficulties, organic chemists, with their wisdom and skills, continue to explore and optimize, hoping to obtain this compound with the simplest method and the highest efficiency, which will contribute to the development of various fields such as medicine and chemical industry.
4-Chloro-2-oxo-3 (2h) -benzothiazoleaceticaci what to pay attention to when storing and transporting
4-Chloro-2-oxo-3 (2H) -benzothiazole acetic acid, this is a fine chemical product. During storage and transportation, special attention should be paid to the following numbers:
First, it is related to storage. This substance should be placed in a cool, dry and well-ventilated place. The cover may be affected by temperature, humidity and air due to its nature. If the temperature is too high, it may cause chemical reactions such as decomposition, which will damage the quality; if the humidity is too high, it is easy to make it damp and cause agglomeration. Therefore, it is crucial to choose a suitable storage environment. In addition, it is necessary to stay away from fire and heat sources because it may be flammable or unstable in heat. And it should be stored separately from oxidants, acids, alkalis, etc., and must not be mixed to prevent dangerous chemical reactions. The storage area should also be equipped with suitable materials to contain leaks, in case of leakage, it can be properly handled in a timely manner.
Second, as for transportation. Make sure that the packaging is complete and sealed before transportation. The packaging material must be able to effectively resist the influence of external factors on the substance and prevent leakage. During transportation, the transportation vehicle should be equipped with the corresponding variety and quantity of fire protection equipment and leakage emergency treatment equipment. The driving route should avoid passing through sensitive areas such as densely populated areas and water source protection areas to prevent serious consequences in the event of an accident. When transporting, follow the specified route and do not stop in residential areas and densely populated areas. Handle with care during loading and unloading to avoid impact, friction, drop, etc., to prevent material leakage due to package damage.
All of these are the areas that need close attention when storing and transporting 4-chloro-2-oxo-3 (2H) -benzothiazole acetic acid to ensure its quality and safety.