Thiophene 2 2 Nitroethenyl
quinoline thiophene imidazole thiazole

Thiophene, 2-(2-nitroethenyl)-

Taiy Chemical

    Specifications

    HS Code

    469944

    Chemical Formula C6H5NO2S
    Molar Mass 155.17 g/mol
    Appearance Solid
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents
    Stability Stable under normal conditions

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    General Information
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    Frequently Asked Questions

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

    What are the physical properties of thiophene, 2- (2-nitrovinyl) -?
    The material properties of 2 - (2 - cyanoethyl) are an important research in the field of chemistry. This compound, in terms of its physical properties, is mostly liquid at room temperature and pressure. Due to the cyanide group in its molecular structure, it has a specific polarity, and due to the existence of carbon chains, it has a certain solubility. In common organic solvents, such as ethanol and ether, it can show good solubility. This property is due to the matching of the forces between molecules, just like tenon-mortise fit, the Van der Waals force and hydrogen bond between the molecules of the organic solvent and the 2 - (2 - cyanoethyl) molecules promote the interaction between the two.
    Looking at its chemical properties, the cyanyl group is an active group, which makes 2- (2-cyanoethyl) have many reactive activities. The cyanyl group can participate in the nucleophilic addition reaction, just like a warrior who is brave enough to go to the battlefield. When encountering nucleophilic reagents, the carbon atoms in the cyanyl group can be attacked by nucleophilic reagents, and then a series of transformations occur, resulting in the derivation of many new compounds. For example, when reacted with water under certain conditions, it can hydrolyze to form carboxylic acid derivatives. This process is like a wonderful chemical transformation, and the molecular structure is recombined, and the properties are also changed.
    At the same time, 2 - (2 - cyanoethyl) is connected by the carbon chain, and the hydrogen atoms on the carbon chain also have certain activity. Under appropriate conditions, substitution reactions can occur, such as halogenation reactions. Halogen atoms can replace hydrogen atoms on the carbon chain, thus endowing compounds with new chemical properties and application potential. In short, the physical and chemical properties of 2 - (2 - cyanoethyl) determine its wide application and research value in many fields such as organic synthesis and materials science, paving the way for many chemical explorations and industrial practices.
    What are the chemical properties of thiophene, 2- (2-nitrovinyl) -?
    The chemical substance of 2 - (2 -cyanoethyl) - is beta-cyanoethanol. This substance has many chemical properties.
    Its appearance is usually a colorless to light yellow liquid with a weak odor. It can be seen from its chemical structure containing cyanide and hydroxyl groups that it has both characteristics.
    Let's talk about cyanyl first, which makes it reactive. Under suitable conditions, cyanyl can undergo hydrolysis. In case of acid or alkali, cyanyl will gradually hydrolyze to form amides, and then further hydrolyze to form carboxylic acids and ammonia. Take hydrolysis under alkaline conditions as an example. The alkali provides hydroxide ions and attacks the carbon atoms of the cyanyl group. After a series of intermediate steps, carboxylate and ammonia are finally formed. This reaction is an important method for preparing the corresponding carboxylic acid.
    The hydroxyl group gives it hydrophilicity and can form hydrogen bonds with water molecules, so β-cyanoethanol can be mutually soluble with water in a certain proportion. At the same time, the hydroxyl group can participate in the esterification reaction. Under acid catalysis, it can react with carboxylic acids. The hydrogen atom in the hydroxyl group combines with the hydroxyl group of the carboxylic acid to form water, and the remaining part is connected to form an ester. For example, when reacted with acetic acid, beta-cyanoethyl acetate will be formed.
    In addition, β-cyano The hydrogen atom of the hydroxyl group can be replaced by other groups, such as reacting with halogenated hydrocarbons under basic conditions, and the halogen atom replaces the hydroxyl hydrogen to form a new organic compound. This reaction is used in organic synthesis to introduce different functional groups and expand the diversity of molecular structures. In short, β-cyanoethanol is widely used in organic synthesis, chemical industry and other fields due to its rich chemical properties of cyano and hydroxyl groups.
    In which fields is thiophene, 2- (2-nitrovinyl) - used?
    2 - (2 -cyanoethylfuranyl) is used in many fields. In the field of medicine, it can be used as a key raw material for drug synthesis. Due to its unique chemical structure, it can be combined with many bioactive molecules to help develop new drugs, such as targeted drugs for specific diseases. By accurately acting on diseased cells, it can improve the therapeutic effect and reduce side effects.
    In the field of materials science, it also has extraordinary value. It can be used to prepare high-performance polymer materials, giving materials unique physical and chemical properties. Such as enhancing the stability, heat resistance and mechanical properties of materials. Polymers synthesized with this substance may be used in high-end fields such as aerospace and electronic equipment to meet the stringent performance requirements of materials.
    Furthermore, in the field of organic synthetic chemistry, it is an extremely important intermediate. With its special functional groups, complex organic molecular structures can be constructed through various chemical reactions. Chemists can use this as a starting material to carry out various novel synthetic route designs, enrich the variety of organic compounds, and inject new vitality into the development of organic synthetic chemistry.
    In addition, in the fragrance and essence industry, its unique odor characteristics may provide the possibility of formulating new fragrances. After being cleverly matched and blended, a unique aroma can be created, which can be used in perfumes, cosmetics, and food additives to enhance the olfactory experience and market competitiveness of products.
    What is the synthesis method of thiophene, 2- (2-nitrovinyl) -?
    To prepare 2 - (2 - cyanoethoxy) ethanol, the synthesis method is as follows:
    First take an appropriate amount of acrylonitrile and place it in a clean reaction vessel. Another amount of ethylene glycol is slowly poured into the container containing acrylonitrile. The reaction of the two requires the participation of suitable catalysts, generally basic catalysts such as sodium hydroxide can be selected. Under suitable temperature and pressure conditions, the addition reaction of the two occurs.
    When reacting, pay close attention to the change of temperature. If the temperature is too high, the side reactions will increase and the product will be impure; if the temperature is too low, the reaction rate will be slow and take a long time. Generally speaking, the reaction temperature is preferably controlled at 50 ° C to 70 ° C, and the pressure can be maintained near normal pressure.
    After the reaction is completed, the reaction mixture is separated and purified. Distillation can be used to remove unreacted acrylonitrile and ethylene glycol. Since the boiling points of acrylonitrile and ethylene glycol are different from the product 2 - (2 - cyanoethoxy) ethanol, they can be separated by distillation. After that, the product is further purified by extraction to obtain high-purity 2 - (2 - cyanoethoxy) ethanol.
    This synthesis method, although seemingly clear steps, in practice, the control of the reaction conditions is extremely critical, and a slight error may affect the yield and purity of the product. Therefore, the operator needs to exercise caution and precisely control the reaction parameters.
    Is thiophene, 2- (2-nitrovinyl) - harmful to the environment and human health?
    Fu 2 - (2 -cyanoethyl hydroxyl) - Whether it is harmful to the environment and human body is an important matter for people's livelihood. Today, it is stated in the ancient text of "Tiangong Kaiwu".
    Cyanoethyl hydroxyl substances may be useful in the field of chemical industry. However, its impact on the surrounding environment and human body cannot be ignored.
    Looking at the natural environment, if this substance is wantonly released outside, or soils the soil. Soil, the foundation of all things, if its quality changes, the growth and life of plants will be disturbed by it. Or it will cause the plant to fail, or even die prematurely, and then disrupt the ecological order. And when it enters the water body, water is the source of life, and aquatic spirits depend on it. If the water is polluted, fish, turtles, shrimp, crabs and other aquariums will be difficult to survive, and it will also harm the people who live by water. There is no water to use, and their livelihood is worrying.
    As for the human body, if you touch it carelessly, it may cause skin discomfort, itching, redness and swelling; in severe cases, it may damage the texture and damage the viscera. If you inhale its volatile gas, the lungs will bear the brunt, or cause respiratory diseases, cough and chest tightness, and damage the function of the lungs for a long time. If you eat it by mistake, the harm will be even more serious, and the transportation of the viscera may be messed up, endangering your life.
    Therefore, in 2 - (2 - cyanoethyl hydroxyl) this material, be cautious. When using it, there must be a comprehensive method to prevent it from leaking into the environment and preventing harm to the common people. Those who operate should also strictly abide by regulations and use protective equipment to ensure their own safety. In this way, the purpose of using things without harming the environment and people can be achieved, and the whole ecology and human life can be safe.