2-carbamoyl-5-(2-mercapto-1,3-thiazol-4-yl)-thiophene

2 - carbamoyl - 5 - (2 - mercapto - 1,3 - thiazol - 4 - yl) thiophene, an organic compound. Its structure is unique, or it shows important functions in many fields.
In the field of pharmaceutical chemistry, such compounds containing special heterocyclic structures often have biological activity, or can become lead compounds for the development of new drugs. The combination of thiazole and thiophene in its structure may interact with specific targets in the body, such as enzymes, receptors, etc. For example, some drugs containing thiazole structure can bind to enzyme activity checking points to regulate enzyme activity and achieve the purpose of treating diseases. This compound may have potential effects in antibacterial, anti-inflammatory, anti-tumor, etc.
In the field of materials science, due to its sulfur-containing atoms, it may endow materials with special electrical and optical properties. Sulfur-containing compounds have attracted much attention in the field of organic semiconductor materials, and may be used to prepare organic Light Emitting Diodes (OLEDs), organic field effect transistors (OFETs) and other devices. The compound may exhibit good carrier transport performance due to its unique structure and improve device performance.
In agricultural chemistry, it may have insecticidal and bactericidal activities. Some compounds containing heterocyclic structures can interfere with the normal physiological metabolism of pests and pathogens, achieving control effects. Its unique structure may accurately act on specific physiological processes of pests and pathogens, making it a candidate for green and efficient pesticide research and development.
In summary, 2-carbamoyl-5- (2-mercapto-1,3-thiazol-4-yl) thiophene has potential application value in the fields of medicine, materials, and agricultural chemistry due to its special structure. It is expected to be further researched and developed to contribute to the development of various fields.

2 - carbamoyl - 5 - (2 - mercapto - 1,3 - thiazol - 4 - yl) thiophene is an organic compound with unique chemical properties and important significance in many fields.
Its structure contains thiophene and thiazole heterocycles, as well as aminocarboxyl and mercapto groups. Thiophene and thiazole heterocycles endow the compound with certain aromaticity, making the molecule more stable and showing specific activities in chemical reactions. The distribution of electron clouds in aromatic systems makes it prone to electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. Electrophilic reagents can attack the higher electron cloud density sites on the ring.
Aminoformyl groups (-CONH ²) have a certain polarity and can participate in the formation of hydrogen bonds. This property affects the physical properties of the compound, such as solubility, or enhances its solubility in polar solvents. And the aminoformyl groups can undergo hydrolysis reaction. Under acidic or basic conditions, they can be hydrolyzed to form corresponding carboxylic acids and ammonia or amines. This reaction can be used in organic synthesis for functional group conversion.
Mercapto (-SH) has high activity and is easily oxidized. Under the action of mild oxidants, disulfide bonds (-S-S -) can be formed. This reaction is often used for the structural stabilization of proteins and polypeptides and some organic synthesis steps. At the same time, sulfhydryl groups have nucleophilic properties, which can undergo nucleophilic substitution or addition reactions with halogenated hydrocarbons, aldides, ketones and other electrophilic reagents. This property is crucial when constructing new carbon-sulfur bonds or introducing other functional groups.
Due to the coexistence of multiple functional groups in the molecule, different functional groups may interact with each other, changing each other's activity and reaction selectivity. When designing a synthetic route or studying its reaction, it is necessary to consider the interaction of each functional group comprehensively.
This compound is rich in chemical properties and lays a foundation for research and application in organic synthesis, medicinal chemistry and other fields. Through rational utilization of its properties, materials with unique functions can be prepared, or drugs with specific biological activities can be developed.

To prepare 2-carbamoyl-5- (2-mercapto-1,3-thiazol-4-yl) thiophene, the method is as follows:
Take the appropriate starting material first, and the synthesis may need to be based on compounds containing thiazole and thiophene structures. Or active halogenated thiophene derivatives can be used to react with thiazole compounds containing mercapto groups.
In the reaction system, select suitable solvents, such as polar organic solvents, such as dimethylformamide (DMF) or dichloromethane, to help the reactants dissolve and the reaction proceeds. < Br > Add an appropriate amount of alkali, such as potassium carbonate or triethylamine, etc., which can promote the reaction, adjust the pH of the reaction environment, and assist the nucleophilic substitution reaction.
Control the reaction temperature, depending on the reactant activity and reaction process, or at room temperature, or need to be heated to a certain temperature, such as 50-80 ° C, and maintain an appropriate time to achieve complete reaction.
After the reaction is completed, the product is treated by common separation and purification methods. For example, by extraction, use a suitable organic solvent to separate from the aqueous phase, and retain the organic phase. After column chromatography, the appropriate silica gel column and eluent were selected to separate the product from the impurities to obtain pure 2-carbamoyl-5- (2-mercapto-1,3-thiazol-4-yl) thiophene. The whole process needs to pay attention to the precise control of reaction conditions and the operation specifications of each step to improve the yield and purity of the product.

There is a question today, what is the market price of 2-carbamoyl-5- (2-mercapto-1,3-thiazol-4-yl) thiophene. This is a chemical substance, and its price varies for a variety of reasons.
First, the difficulty of its preparation depends on the price. If the preparation method is difficult, many delicate steps, precious raw materials, and harsh reaction conditions are required, such as temperature control, pressure control, and special catalysts, the cost will be high, and the price will be high.
Second, the price of raw materials is also key. If the raw materials used to prepare this compound are scarce or difficult to obtain, the price will rise.
Third, the market supply and demand affect its price. If there is a lot of demand and the supply is insufficient, the merchant will raise the price; if the demand is weak and the supply is excessive, the price will tend to drop.
Fourth, the purity of the product has a great impact on the price. For high purity, the preparation is more difficult, the cost is higher, and the price is also high; for low purity, the cost is low and the price is also low.
However, I have checked the classics all over the world, but I have not obtained the exact price of this product at the moment. To know the price, you can consult the supplier of chemical raw materials, or check the platform and market of chemical product trading in detail to get a near-real price.

2 - carbamoyl - 5 - (2 - mercapto - 1, 3 - thiazol - 4 - yl) thiophene, this is a rather special organic compound. To explore its manufacturer requires visiting various chemical fields.
In today's world, many leaders in fine chemical production are often involved in the production of such compounds. However, finding a manufacturer of this compound is like finding a rare herb hidden in the mountains, which requires a lot of trouble.
In the Eastern Domain, there are several factories focusing on fine chemical synthesis, which have been studying the art of organic synthesis for many years, or have the production process of this compound. They use ingenious methods to combine various raw materials, and after many reactions, they finally obtain this product.
In Western countries, there are also chemical giants, with advanced equipment and exquisite skills, engaged in the production of this compound. Its research and development power is strong, and it can precisely control the details of the reaction to ensure the quality of the product.
In addition, in the north and south, there are also many manufacturers specializing in specialty chemicals. They are deeply involved in specific fields, and may also have unique characteristics in the production of this compound. Or by virtue of unique formulas or relying on innovative processes, they can win a place in the production of this compound.
If you want to know the exact manufacturer of this compound, you should go through the classics of chemical information, visit the industry, explore the traces of chemical exhibitions, or obtain accurate information to find the required manufacturer.