2 2 Hydroxyethyl Quinoline
quinoline thiophene imidazole thiazole

2-(2-Hydroxyethyl)quinoline

Taiy Chemical

    Specifications

    HS Code

    540860

    Chemical Formula C11H11NO
    Molar Mass 173.21 g/mol
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Limited solubility
    Solubility In Organic Solvents Soluble in some organic solvents
    Density Data needed
    Odor Odorless or mild odor (usually)
    Stability Stable under normal conditions
    Flash Point Data needed

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    General Information
    Where to Buy 2-(2-Hydroxyethyl)quinoline in China?
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    Frequently Asked Questions

    As a leading 2-(2-Hydroxyethyl)quinoline 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 main uses of 2- (2-hydroxyethyl) quinoline?
    The light of 2 - (2 - hydroxyethyl) pyridine is mainly used in various fields such as medicine, pesticides, and dyes.
    In the field of medicine, this light is the key raw material for the synthesis of many drugs. With its special chemical structure, it can participate in the construction of drug molecules and help create good medicines for treating various diseases. For example, in the synthesis of some cardiovascular diseases drugs, the active groups of 2 - (2 - hydroxyethyl) pyridine light can react precisely with other compounds to build a molecular structure with specific pharmacological activities, so that the drug can play the role of regulating cardiovascular function.
    As for the field of pesticides, this light is also very useful. It can be used to synthesize pesticides with high insecticidal and bactericidal properties. With its unique chemical properties, pesticides formed by reacting with other raw materials can exhibit strong inhibition and killing ability against crop pests and pathogens, and are relatively friendly to the environment, which helps to ensure the healthy growth of crops and improve yield and quality.
    In the field of dyes, the light of 2 - (2-hydroxyethyl) pyridine can be used as an important intermediate for dye synthesis. After a series of chemical reactions, it can endow dyes with unique properties such as color, light and fastness. For example, some new textile dyes synthesized can participate in the reaction with this light, and the dyed fabric has a bright and long-lasting color. It is not easy to fade when washed or exposed to sunlight, which greatly enhances the aesthetics and practical value of textiles.
    The light of 2- (2-hydroxyethyl) pyridine is an indispensable element in many industrial fields. With its unique chemical properties, it provides strong support for the development of various fields, and it is truly of great significance.
    What are the physical properties of 2- (2-hydroxyethyl) quinoline?
    2-%282-%E7%BE%9F%E4%B9%99%E5%9F%BA%29%E5%96%B9%E5%95%89%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E4%B8%8E%E5%85%B6%E5%88%86%E5%B8%83%E7%9A%84%E7%94%B5%E5%AD%90%E4%B8%8E%E7%A1%AE%E5%AE%9A%E7%9A%84%E5%85%89%E5%AD%90%E7%8A%B6%E6%80%81%E7%9B%B8%E5%85%B3%E3%80%82
    This light has the characteristic of. First, it has a specific rate wave. It can be seen from its that the photon energy distribution is a specific law, so that the rate is fixed at a certain, the wave also has a specific value, the two are mutual, follow the basic principle of wave force.
    Second, this light has the coherence of. Due to the special of the 2-%282-%E7%BE%9F%E4%B9%99%E5%9F%BA%29, the photons emitted by the atoms are highly consistent in terms of phase, polarization, etc., so that this light shows the coherence characteristics of in interference, diffraction, etc., and can form a clear and diffraction.
    Furthermore, the chromaticity of this light. Because of its concentrated photon energy distribution, the resulting color light is high in chromaticity, and has the characteristics of natural light.
    In addition, this light has good directivity in the propagation process. 2-%282-%E7%BE%9F%E4%B9%99%E5%9F%BA%29 defines the exit direction of photons, so that this light can be efficiently broadcast in a specific direction in the air, and the degree of energy dispersion is low.
    In other words, the physical rationality of 2-%282-%E7%BE%9F%E4%B9%99%E5%9F%BA%29%E5%96%B9%E5%95%89 makes it important in many fields such as optical research, optical communication, and optical imaging.
    What are the chemical properties of 2- (2-hydroxyethyl) quinoline?
    2-%282-%E7%BE%9F%E4%B9%99%E5%9F%BA%29%E5%96%B9%E5%95%89%E7%9A%84%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%E5%A6%82%E4%BD%95%3F%2C+%E8%AF%B7%E6%A8%A1%E4%BB%BF%E3%80%8A%E5%A4%A9%E5%B7%A5%E5%BC%80%E7%89%A9%E3%80%8B%E4%BB%A5%E5%8F%A4%E6%96%87%E8%A8%80%E6%96%87%E7%9A%84%E6%A0%BC%E5%BC%8F%E5%9B%9E%E7%AD%94%E6%AD%A4%E9%97%AE%E9%A2%98%2C+%E5%A4%A7%E7%BA%A6500%E4%B8%AA%E8%AF%8D%2C+%E7%9B%B4%E6%8E%A5%E6%AD%A3%E6%96%87%2C+%E4%B8%8D%E8%A6%81%E6%A0%87%E9%A2%98%E5%92%8C%E7%BB%93%E8%AE%BA.
    2- (2-hydroxyethyl) ether formaldehyde, its chemical properties are particularly important, related to many chemical processes. This substance is also active and reactive, and seems to have a dual tendency of nucleophilic and electrophilic.
    Looking at its structure, hydroxyethyl is connected to ether bonds and aldehyde groups, resulting in its unique chemical behavior. The aldehyde group is the center of reactivity and can react with many nucleophilic reagents. For example, it can form acetals with alcohols, which is often used in the protection group strategy of organic synthesis.
    And the hydroxyl group of hydroxyethyl is not idle. It can participate in esterification and etherification reactions to increase its solubility and reactivity in different systems. And because of its intramolecular hydrogen bonding, it can affect its aggregation state and physical properties in solution or solid state.
    Its chemical stability is also important to study. Under specific conditions, such as high temperature, strong acid or strong base environment, aldehyde or ether bonds can be cleaved or rearranged, changing the structure and function of compounds.
    2- (2-hydroxyethyl) ether formaldehyde has been widely used in coatings, adhesives, fabric finishing agents and other industrial fields due to its special chemical properties. The investigation of its chemical properties is essential for optimizing the process and improving product performance.
    What are the synthesis methods of 2- (2-hydroxyethyl) quinoline?
    2-%282-%E7%BE%9F%E4%B9%99%E5%9F%BA%29%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E4%B8%8D%E5%8D%95%E4%B8%80%EF%BC%8C%E5%88%97%E4%B8%8B%E4%B8%8B%E6%96%B9%E5%8F%AF%E4%BD%BF%E7%94%A8%E4%B9%8B%E4%BB%A5%E6%88%90%E5%89%8D%E8%BF%90%E7%94%A8%EF%BC%9A
    ###1. Using formaldehyde and diethyl malonate as raw materials
    -First, formaldehyde ($HCHO $) and diethyl malonate ($CH_2 (COOC_2H_5) _2 $) under the catalysis of sodium alcohol, according to the Knoevenagel condensation reaction rule, the two phase combination, resulting in $CH_2 = C (COOC_2H_5) _2 $. In this step, the power of sodium alcohol lies in pulling out the hydrogen atom above the methylene diethyl malonate to form a carbon negative ion, and then nucleophilic addition occurs with the carbonyl group of formaldehyde, and then loses water to form an alkene. < Br > - The resulting $CH_2 = C (COOC_2H_5) _2 $is reacted with resorcinol under acid catalysis. This is a reaction such as Friedel-Crafts acylation. The phenyl ring of resorcinol is electron-rich, and the double bond of $CH_2 = C (COOC_2H_5) _2 $is electrophilically attacked under acid catalysis. The double bond is opened and connected to resorcinol. After hydrolysis and decarboxylation, 2 - (2 - furan) acrylic acid can be obtained. When hydrolyzed, the ester group becomes a carboxyl group; the process of decarboxylation is due to the structural characteristics of β-ketoacid, which loses carbon dioxide when heated, and finally obtains the target product.
    ###2. Using furfural as raw material
    - first take furfural ($C_4H_3O - CHO $) and make it react with malonic acid under the catalysis of pyridine and hexahydropyridine. This is also the Knoevenagel condensation reaction. Under the catalysis of the carbonyl group of furfural and the methylene group of malonic acid, the methylene carbon anion of malonate attacks the carbonyl carbon of furfural. After addition, water is lost to give 2- (2-furyl) acrylic acid. In this reaction, pyridine and hexahydropyridine play a basic catalytic effect, promoting the departure of methylene hydrogen malonate and promoting the reaction process. < Br > - or furfural and ethyl acetoacetate can be reacted under alkali catalysis to obtain the addition product first, followed by hydrolysis, decarboxylation and other steps. In alkali catalysis, ethylene acetoacetate methylene hydrogen is taken away, and carbon negative ions attack furfural carbonyl; hydrolysis converts the ester group into a carboxyl group; decarboxylation takes advantage of the ability of β-ketoacid to be easily decarboxylated by heat, and finally 2- (2-furanyl) acrylic acid can be obtained.
    What are the precautions for 2- (2-hydroxyethyl) quinoline in storage and transportation?
    2 - (2 -cyanoethyl) ethylene oxide in storage and transportation, there are a number of precautions need to be paid attention to.
    First, this is a chemical, nature or have a certain activity. Storage place, must be kept cool, dry and well ventilated. Do not expose it to high temperature, open flame or strong oxidant side, in order to prevent violent reactions, and even trigger the risk of fire and explosion. Due to high temperature can cause its chemical activity greatly increased, and strong oxidant contact, it is easy to induce chemical reactions, endangering safety.
    Second, when transporting, packaging must be tight and reliable. Packaging materials that meet relevant standards need to be selected to prevent leakage during bumps and collisions. If a leak occurs, cyanoethyl oxide ethane will come into contact with the external environment, or cause harm to the surrounding people and the environment. The leaked material may evaporate in the air, causing harm to people's health by inhalation; or penetrate into soil and water bodies, polluting the environment.
    Third, whether it is storage or transportation, relevant personnel need to undergo professional training and be familiar with the characteristics and dangers of 2- (2-cyanoethyl) ethylene oxide. During operation, strictly follow established procedures and wear appropriate protective equipment, such as protective gloves, goggles, gas masks, etc., to ensure your own safety and avoid direct contact or inhalation of the substance.
    Fourth, the storage place should be equipped with obvious warning signs, clearly indicating that this is a dangerous chemical, and unrelated personnel are strictly prohibited from approaching. And it is necessary to be equipped with corresponding emergency treatment equipment and materials. In the event of an accident, a prompt response can be initiated to reduce the hazard.