Quinoline 1 2 3 4 Tetrahydro
quinoline thiophene imidazole thiazole

Quinoline, 1,2,3,4-tetrahydro-

Taiy Chemical

    Specifications

    HS Code

    957037

    Chemical Formula C9H11N
    Molar Mass 133.19 g/mol
    Appearance Colorless to pale yellow liquid
    Odor Characteristic, unpleasant odor
    Density 0.99 g/cm³ (at 20 °C)
    Boiling Point 205 - 207 °C
    Melting Point -15 °C
    Solubility In Water Slightly soluble
    Solubility In Organic Solvents Soluble in ethanol, ether, etc.
    Flash Point 77 °C

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    General Information
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    Frequently Asked Questions

    As a leading Quinoline, 1,2,3,4-tetrahydro- 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 property of Quinoline, 1, 2, 3, 4 - tetrahydro -
    Quinoline, 1, 2, 3, 4-tetrahydro-, is one of the organic compounds. Its chemical properties are interesting and have important uses in many fields.
    This compound has unique structural characteristics. Hydrogen atoms are introduced into the quinoline ring at 1, 2, 3, 4 positions through hydrogenation, resulting in changes in the electron cloud distribution and spatial configuration, and the chemical properties are also different.
    In terms of its stability, it is improved compared with quinoline. Due to the reduction of its unsaturated bonds, the conjugate system is affected, resulting in a decrease in molecular energy and enhanced stability. In chemical reactions, this structural change also changes its reactivity. Compared with quinoline, 1, 2, 3, 4-tetrahydroquinoline, it is more prone to nucleophilic substitution. The solitary pair electrons on the nitrogen atom are more likely to participate in the reaction. Due to the change of the surrounding electronic environment after hydrogenation, the electron cloud density of the nitrogen atom increases relatively, and the nucleophilicity is enhanced.
    In terms of solubility, due to structural changes, its solubility in organic solvents may be different. Generally speaking, it is more soluble in polar organic solvents, such as alcohols and ethers, than quinoline. Due to the change of molecular polarity after hydrogenation, the interaction with polar solvents is enhanced.
    And because of its structural characteristics, 1,2,3,4-tetrahydroquinoline is widely used in pharmaceutical chemistry, materials science and other fields. In drug development, it can be used as a key intermediate to build molecular structures with specific biological activities through its reactivity. In the field of material synthesis, it may be introduced into the polymer structure through specific reactions to endow the material with unique properties, such as improving the optical and electrical properties of the material.
    Quinoline, 1, 2, 3, 4 - tetrahydro - in which areas is it used
    Quinoline, 1, 2, 3, 4-tetrahydro - This compound is useful in many fields. In the field of medicine, it is often the key raw material for the creation of drugs. Due to its unique chemical structure, it can interact with many targets in the body to achieve the effect of treating diseases. In the past, doctors often searched for all kinds of strange medicines to cure diseases. This compound is the cornerstone of medical creation, helping doctors find good prescriptions and heal diseases.
    In the field of materials science, 1, 2, 3, 4-tetrahydroquinoline also has extraordinary value. It can be used to prepare materials with special properties, or to increase their strength, or to modify their optical properties. Just as the ancient craftsmen made good use of various materials to create strange things, today's scholars also use them as raw materials to create new materials with excellent performance, which are used in electronics, optics and other fields.
    In the field of organic synthesis, it is an important intermediate. Organic synthesis is like building a delicate pavilion, and 1,2,3,4-tetrahydroquinoline is an indispensable brick and stone. Chemists can use this to build complex organic molecules, synthesize new substances that are not available in nature, and expand the boundaries of organic chemistry, just as the ancients opened up unknown territories, constantly exploring new possibilities.
    In addition, in the fragrance industry, it may contribute a unique aroma. Blending spices, like composing a beautiful movement, 1,2,3,4-tetrahydroquinoline is a unique music note, adding a different flavor to the spices, making the aroma richer and more charming.
    Quinoline, 1, 2, 3, 4 - tetrahydro - what are the preparation methods
    The preparation method of quinoline, 1, 2, 3, 4-tetrahydro- has been known for a long time, and is described in detail below.
    First, quinoline is used as the starting material, and the method of catalytic hydrogenation is used. Choose a suitable catalyst, such as a noble metal catalyst, and make hydrogen react with quinoline under appropriate temperature and pressure conditions. If the temperature is properly controlled, or in a specific range, the pressure is also adjusted moderately, then hydrogen can be gradually added to the unsaturated bond of quinoline, resulting in 1, 2, 3, 4-tetrahydroquinoline. In this process, the activity and selectivity of the catalyst are the key. If the activity is high, the reaction rate is fast, and if the selectivity is good, there are few side reactions, and the purity of the product is guaranteed.
    Second, through the organic synthesis path. A specific intermediate can be prepared first, with nitrogen-containing compounds and hydrocarbons with suitable functional groups as starting materials, through a series of chemical reactions, such as nucleophilic substitution, condensation, etc., to construct an intermediate with a structure similar to 1,2,3,4-tetrahydroquinoline. Subsequently, this intermediate is subjected to a reduction reaction, such as metal hydride and other reducing agents, to reduce specific unsaturated bonds, and finally obtain 1,2,3,4-tetrahydroquinoline. This path requires precise control of the reaction conditions, and the order and reaction conditions of each step will affect the yield and purity of the final product.
    Third, there is a preparation method using natural products as the starting point. Some natural products may contain components related to the structure of 1, 2, 3, 4-tetrahydroquinoline, and the target product can also be prepared through extraction, separation, modification and other steps. However, this method is often subject to the source and content of natural products, and the extraction and modification process is often complicated, requiring fine operation and high-end technology.
    All these preparation methods have their own advantages and disadvantages. In fact, they need to be selected according to the actual needs and conditions, so as to efficiently prepare 1, 2, 3, 4-tetrahydroquinoline.
    What are the physical properties of Quinoline, 1, 2, 3, 4 - tetrahydro -
    Quinoline, 1, 2, 3, 4-tetrahydro-, is a class of organic compounds. Its physical properties are particularly important, and it is related to many uses and characteristics of this compound.
    In terms of color state, 1, 2, 3, 4-tetrahydroquinoline is often colorless to light yellow liquid, and it has a flowing state. It can be seen in ordinary light that its transparent quality is slightly glossy, just like the early gathering of morning dew, clear without losing charm. < Br >
    Smell the smell, which seems to have a special aromatic aroma, but it is not as rich as orchid, nor as sweet as cinnamon. It is a unique organic aromatic smell. At first, it is slightly pungent, but gradually smelling it can sense its unique charm. If placed in a ventilated place, its gas can gradually disperse in the air.
    When it comes to the boiling point, the boiling point of this compound is about 195-200 ° C. When the heating method is applied and the temperature gradually rises to nearly 200 ° C, it can be seen that it gradually transforms from a liquid state to a gaseous state, just like a cloud rising. This boiling point characteristic is crucial in separation and purification processes, so it can be effectively separated from the mixture. < Br >
    The number of melting points is about -12 ° C. When the outside temperature drops to around -12 ° C, the originally flowing liquid gradually solidifies, as if time is static, its state changes from liquid to solid, and the molecular arrangement becomes orderly from disorder. The nature of this melting point needs to be carefully considered during storage and transportation.
    Above the density, the density of 1,2,3,4-tetrahydroquinoline is slightly larger than that of water, about 1.06g/cm ³. If it is placed in the same place as water, it can be seen that it sinks underwater, such as stone entering water. The difference in density can be used as an important basis for judging in some experiments or industrial operations of liquid-liquid separation. In terms of solubility, it is soluble in many organic solvents, such as ethanol, ether, etc., just like fish get water, and the two can be mixed into a uniform state; however, the solubility in water is poor, and the two meet, such as oil floating in water, distinct, this solubility characteristic also affects its reaction and application in different media.
    Quinoline, 1, 2, 3, 4 - tetrahydro - what is the market outlook
    1, 2, 3, 4-tetrahydroquinoline, the prospect of this product in today's market is actually related to the rise and fall of many fields, and it is necessary to explore in detail.
    Looking at the field of medicine, 1, 2, 3, 4-tetrahydroquinoline and its derivatives show extraordinary potential. Because of its unique chemical structure, it can interact with specific targets in organisms, which may open up new avenues for drug research and development. The creation of drugs such as antibacterial, anti-inflammatory, and anti-tumor is expected to expand ideas. Today's pharmaceutical market is hungry for innovative drugs. This compound or a treasure that drug companies are competing to chase. In time, new drugs based on this may come out and treat diseases and diseases for patients. Its market prospects are limitless.
    As for the field of materials, 1,2,3,4-tetrahydroquinoline has also emerged. In the synthesis of polymer materials, it can be used as a key monomer to endow the material with unique properties. Or to enhance the stability of the material, or to improve its optical properties, it has the possibility of application in electronic devices, optical instruments and other industries. With the rapid development of science and technology, the demand for high-performance materials is increasing, and the market space of 1,2,3,4-tetrahydroquinoline in this field will also expand.
    However, the road to market development is not smooth. The complexity of the synthesis process and the high cost may be the key to hindering its large-scale application. Only scientific researchers can study hard, optimize the synthesis method, reduce costs and increase efficiency, and make it unhindered in the market. And the market competition is fierce, it is necessary to speed up the research and development process and seize the opportunity in order to gain a firm foothold in the market.
    To sum up, although 1,2,3,4-tetrahydroquinoline faces challenges, its potential value in the fields of medicine and materials is huge. If it is properly developed and properly operated, the future market prospect is promising, and it is expected to shine on the stage of chemical and related industries.