2 5 Dicyanothiophene
quinoline thiophene imidazole thiazole

2,5-Dicyanothiophene

Taiy Chemical

    Specifications

    HS Code

    528043

    Chemical Formula C6H2N2S
    Molar Mass 134.16 g/mol
    Appearance Solid
    Color Pale yellow to white
    Melting Point 126 - 128 °C
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Crystal Structure Specific crystal packing details would require X - ray analysis
    Thermal Stability Relatively stable under normal conditions, decomposes at high temperatures
    Electron Withdrawing Nature Strong electron - withdrawing groups (cyano) make it electron - deficient
    Reactivity Can participate in various organic reactions such as nucleophilic substitution, cycloaddition reactions

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    Frequently Asked Questions

    As a leading 2,5-Dicyanothiophene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of 2,5-dicyanothiophene?
    2% 2C5 -diethylpyridine, its chemical structure is composed of a pyridine ring and two ethyl groups connected to the 2 and 5 positions of the pyridine ring. The pyridine ring is a nitrogen-containing six-membered heterocyclic ring with aromatic properties. The carbon and nitrogen atoms on the ring are connected by conjugated π bonds, so that the pyridine ring has certain stability and special electron cloud distribution. At the 2 and 5 positions of the pyridine ring, there is an ethyl substituent, respectively. Ethyl is composed of two carbon atoms and five hydrogen atoms. It is connected to the pyridine ring by a carbon-carbon single bond. This structure endows 2,5-diethylpyridine with unique physical and chemical properties. For example, in terms of solubility, due to the presence of ethyl, it may have better solubility than pyridine in some organic solvents; in terms of reactivity, the nitrogen atoms on the pyridine ring and the position of the substituent will affect the difficulty of electrophilic substitution, nucleophilic substitution and other reactions and the reaction check point.
    The structure of 2,5-diethylpyridine is based on the pyridine ring, and the two and five positions are connected to one ethyl. The pyridine ring contains nitrogen and has aromatic properties. The carbon and nitrogen atoms in the ring are linked by a conjugated π bond, which is stable and the electron cloud is divided. The di- and pentahydride-linked ethyl groups are formed by dicarbon pentahydride and are linked to pyridine by a carbon-carbon single bond. This structure makes it have unique physical and chemical properties, such as solubility. Because of ethyl, it is better than pyridine in some organic solvents or dissolves. In terms of reactivity, the position of the nitrogen atom and the substituent of the pyridine ring affects the difficulty and check point of electrophilic and nucleophilic substitution reactions.
    What are the main uses of 2,5-dicyanothiophene?
    2% 2C5 -dihydroxybenzoic acid, also known as gentianic acid, is an important organic compound with critical uses in many fields.
    - ** Pharmaceutical field **: It has certain biological activity and pharmacological properties. On the one hand, it can be used as an intermediate for drug synthesis. In the preparation process of many drugs, gentianic acid can be chemically modified and transformed into the molecular structure of the drug to give the drug a specific therapeutic effect. For example, in the synthesis of some anti-inflammatory and antibacterial drugs, gentianic acid is an important starting material. On the other hand, studies have shown that it may have anti-oxidant and other physiological activities, which can help the human body resist free radical damage, or play a potential preventive and therapeutic role in some oxidative stress-related diseases, such as cardiovascular diseases and neurodegenerative diseases.
    - ** Chemical field **: In the chemical industry, gentian acid can be used to synthesize special functional materials. For example, in the preparation of some polymer materials, the introduction of dragon cholic acid as a functional monomer can give the material unique properties, such as improving the stability and hydrophilicity of the material. In addition, in the coating industry, it can be used as an additive to improve the adhesion and corrosion resistance of coatings. < Br > - ** Cosmetics field **: In view of its antioxidant properties, gentian acid can be added to cosmetics. It can help the skin resist free radical damage induced by ultraviolet rays, environmental pollution and other factors, delay skin aging, reduce wrinkles, and may have a certain whitening effect. It can inhibit melanin production, brighten skin tone, and improve the overall condition of skin.
    What are the physical properties of 2,5-dicyanothiophene?
    2% 2C5-dihydroxybenzoic acid, also known as gentian acid, is an important organic compound. It has many unique physical properties and has important uses in many fields.
    Looking at its properties, 2,5-dihydroxybenzoic acid is a white to light yellow crystalline powder at room temperature. This form is easy to store and transport, and it is easy to mix with other substances, providing convenience for subsequent applications. Its melting point is between 200-204 ° C, and its melting point is high, indicating that its intermolecular force is strong and its structure is relatively stable. This stability allows the substance to maintain its inherent form and properties within a certain temperature range, and can exist stably in reactions or processes that require high temperature treatment. It does not easily decompose or other adverse reactions occur.
    Solubility is also one of its important physical properties. 2,5-Dihydroxybenzoic acid is slightly soluble in water, but easily soluble in organic solvents such as ethanol and ether. The characteristics of slight solubility in water determine its dispersion and reaction mode in water systems; and its good solubility to organic solvents makes it possible to use organic solvents as reaction media or extraction solvents in organic synthesis, drug preparation and other fields to achieve full mixing and reaction with other organic substances, greatly expanding its application range.
    Furthermore, 2,5-Dihydroxybenzoic acid has certain sublimation properties. Although the sublimation conditions are more harsh, it can be directly converted from solid to gaseous state at specific temperatures and pressures. This sublimation property is used in some fine chemical fields, such as the purification and separation process of substances, or the sublimation characteristics can be used to separate it from impurities to obtain high-purity products.
    In addition, the substance has a certain sensitivity to light and heat. Long-term exposure to light or high temperature environment, or decomposition, oxidation and other reactions, cause its structure and properties to change. Therefore, in the process of storage and use, measures such as protection from light and low temperature should be taken to ensure its quality and performance stability.
    To sum up, the physical properties of 2,5-dihydroxybenzoic acid determine its application direction and method in many fields such as chemical industry, medicine, materials, etc. In-depth understanding and rational use of these properties can give full play to its value.
    What are the synthesis methods of 2,5-dicyanothiophene?
    2% 2C5 -dihydroxybenzoic acid, also known as gentian acid, its synthesis method is not recorded in ancient books, but according to today's chemical knowledge, it can be described using ancient methods.
    First, salicylic acid is used as the starting material, which can be analogous to the ancient "transformation" method. Salicylic acid is acylated, and acetic anhydride or acetyl chloride is used as the acylation reagent. Under the action of appropriate "temperature" (temperature) and "auxiliary" (catalyst, such as concentrated sulfuric acid), acetylsalicylic acid is obtained. This step is like ancient alchemy, and it is crucial to control the temperature and dosage. Then, acetylsalicylic acid is hydrolyzed in an alkaline environment, such as sodium hydroxide solution, under suitable conditions, so that the acetyl group is separated, and then acidified. The pH is adjusted with dilute sulfuric acid or hydrochloric acid, and 2% 2C5-dihydroxybenzoic acid is precipitated.
    Second, resorcinol is used as the starting material. Under high pressure and the presence of a suitable "catalyst" (catalyst), resorcinol and carbon dioxide undergo carboxylation reaction, which is similar to the ancient people's specific environment to promote the transformation of substances. Carbon dioxide is like "reiki", injected into the resorcinol structure to generate 2% 2C5-dihydroxybenzoic acid. This process requires strict pressure, temperature and catalyst requirements, and requires fine regulation to obtain the ideal yield and purity.
    Third, it can be extracted from natural products and then transformed. If some plants contain similar structural components, they can be extracted by ancient extraction methods, using water or organic solvents, such as ethanol, etc. After separation, purification, and chemical conversion steps, 2% 2C5-dihydroxybenzoic acid can be obtained through hydrolysis, oxidation or other suitable reactions. This approach requires detailed research on the source of natural products, extraction conditions, and precise chemical conversion methods.
    What are the precautions for the application of 2,5-dicyanothiophene?
    2% 2C5-dihydroxybenzoic acid, in various applications, there are many things to pay attention to. This substance has a certain chemical activity, and when using it, the first thing to pay attention to is its stability. Because it contains dihydroxyl groups, it is easy to oxidize, so it needs to be properly stored to avoid contact with strong oxidants and air for a long time to prevent deterioration and change the properties and efficacy.
    Furthermore, it is related to its solubility. 2% 2C5-dihydroxybenzoic acid dissolves differently in different solvents, and has a certain solubility in water and alcohol solvents. However, when applying, it is necessary to carefully select a suitable solvent according to specific needs to ensure that it is evenly dispersed and fully effective. And in the process of preparing the solution, temperature has a great influence on its dissolution rate and solubility. If necessary, temperature control operation is required to obtain a solution of precise concentration.
    Repeat, toxicity and safety cannot be ignored. Although it is not highly toxic, it should still avoid direct contact with the skin and eyes. If it is accidentally touched, rinse with a lot of water as soon as possible. If you feel unwell, seek medical attention urgently. During production and use, safety procedures should also be followed, and protective equipment such as gloves and goggles should be prepared to protect the safety of operators.
    In addition, 2% 2C5-dihydroxybenzoic acid plays a variable role in chemical reactions, and can be used as a reactant, catalyst or intermediate. Therefore, when participating in a specific reaction, it is necessary to precisely control the dosage and reaction conditions, such as temperature, pH, reaction time, etc. Minor changes in conditions, or changes in the direction of the reaction and the proportion of the product, affect the final result.
    In short, with 2% 2C5-dihydroxybenzoic acid, it is necessary to comprehensively consider the stability, solubility, safety and reaction conditions, and operate cautiously to ensure the effectiveness and safety of its application.