1 2 3 4 Tetrahydro 7 Nitroquinoline
quinoline thiophene imidazole thiazole

1,2,3,4-Tetrahydro-7-nitroquinoline

Taiy Chemical

    Specifications

    HS Code

    152305

    Chemical Formula C9H10N2O2
    Molecular Weight 178.19 g/mol
    Appearance Solid (usually)
    Melting Point Data needed
    Boiling Point Data needed
    Solubility In Water Low (estimated)
    Solubility In Organic Solvents Soluble in some organic solvents (e.g., ethanol, dichloromethane)
    Density Data needed
    Flash Point Data needed
    Pka Data needed
    Logp Data needed
    Stability Stable under normal conditions, may be sensitive to light and air

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    General Information
    Where to Buy 1,2,3,4-Tetrahydro-7-nitroquinoline in China?
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    Frequently Asked Questions

    As a leading 1,2,3,4-Tetrahydro-7-nitroquinoline 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 1,2,3,4-tetrahydro-7-nitroquinoline?
    1% 2C2% 2C3% 2C4-tetrahydro-7-quinolinobenzoic acid has a wide range of main uses.
    This compound is of great benefit in the field of medicine. Cover because of its unique chemical structure, or can be used as a key part of the active ingredient of drugs. Pharmaceutical researchers often observe its interaction with specific targets in organisms, hoping to create new drugs to treat various diseases, such as some chronic diseases, intractable diseases, etc. It may be able to precisely act on specific receptors of diseased cells to regulate cell physiological functions and inhibit the proliferation of diseased cells. It is like a good doctor giving a miracle medicine and treating the symptoms.
    In the field of materials science, it also has extraordinary performance. Or it can be integrated into new materials through specific processes, giving the material unique optical, electrical or mechanical properties. For example, in optoelectronic device materials, it may improve the photosensitivity of the material, making the device respond more keenly and accurately to light signals, so that the efficiency of optoelectronic devices can be improved, just like injecting a smart soul into optoelectronic devices, making their operation more efficient.
    Furthermore, in the field of organic synthesis, this compound is like a delicate "key", opening up a way for the synthesis of complex organic molecules. Chemists can use its special structure and reactivity to build more complex and novel organic frameworks, enrich the variety of organic compounds, and contribute to the development of organic synthesis chemistry, helping organic synthesis to a new height.
    What are the physical properties of 1,2,3,4-tetrahydro-7-nitroquinoline?
    The unique optical properties of 1% 2C2% 2C3% 2C4-tetrahydro-7-quinolinylbenzoic acid are the focus of many scholars. This compound has a chiral center, so it has optical rotation. When plane polarized light passes through the medium containing the substance, the polarization surface rotates, and its optical rotation varies according to the concentration of the substance, the length of the optical path and the wavelength of the incident ray.
    Furthermore, the compound may have fluorescence properties. Due to the conjugated system of the molecular structure, after being excited by a specific wavelength of light, the electron transitions to a high energy level, and then returns to the ground state to release energy in the form of light, and then fluoresces. The position and intensity of the fluorescence emission spectrum are closely related to the molecular structure, and the degree of conjugation, the type and position of the substituents can all affect it. With a high degree of conjugation, the fluorescence emission wavelength or redshift, and the intensity may also be enhanced. Different substituents, electron-withdrawing groups or electron-giving groups, will change the distribution of molecular electron clouds, which in turn affects the fluorescence properties.
    In addition, its optical properties are also reflected in the refractive index. The refractive index of a substance reflects the ratio of the speed of light propagation in it to the speed of propagation in vacuum. The refractive index of this compound is influenced by the molecular structure and external conditions. When the temperature increases, the thermal motion of the molecule intensifies, and the light scattering increases, and the refractive index decreases. Changes in pressure, molecular spacing and interactions also cause changes in ref
    1% 2C2% 2C3% 2C4-tetrahydro-7-quinolinobenzoic acid is rich in optical properties and has broad potential applications in optical materials, biological imaging and other fields.
    What are the chemical properties of 1,2,3,4-tetrahydro-7-nitroquinoline?
    1% 2C2% 2C3% 2C4-tetrahydro-7-benzylcoumarin is an organic compound with the following chemical properties:
    1. ** Solubility **: This compound has good solubility in organic solvents due to its structure containing multiple aromatic rings and ester groups. For example, common organic solvents such as chloroform, dichloromethane, and acetone can make 1% 2C2% 2C3% 2C4-tetrahydro-7-benzylcoumarin well soluble. However, its solubility in water is poor, because the molecular polarity is weak, and the interaction with water molecules is not strong.
    2. ** Stability **: Under normal conditions, 1% 2C2% 2C3% 2C4-tetrahydro-7-benzyl coumarin has certain stability. However, the ester group in its structure can undergo hydrolysis reaction under the catalysis of acid or base. Under acidic conditions, the ester group is gradually hydrolyzed to generate corresponding carboxylic acids and alcohols; under alkaline conditions, the hydrolysis reaction is more rapid, generating carboxylic salts and alcohols.
    3. ** Reactive activity **: The double bonds in its molecules can undergo addition reactions. For example, addition occurs with electrophilic reagents such as halogen elements and hydrogen halides to generate halogenated products. The aromatic ring part can undergo electrophilic substitution reaction. Due to the electron-giving effect of benzyl group, the electron cloud density of the aromatic ring increases, and it is easier to react with electrophilic reagents, such as nitrification, halogenation, sulfonation and other electrophilic substitution reactions. In addition, the structural part of coumarin endows it with certain fluorescent properties, which can fluoresce under specific wavelength light irradiation, which makes it have potential application value in fluorescent materials and other fields.
    What are the synthesis methods of 1,2,3,4-tetrahydro-7-nitroquinoline?
    1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2-7-%E7%A1%9D%E5%9F%BA%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E5%A4%9A%E6%9C%89%E5%90%84%E7%A7%8D%E5%90%84%E6%A0%B7%E4%B9%8B%E9%87%8F%E3%80%82%E6%9D%A5%E8%87%B4%E5%8F%A4%E4%BB%A3%E5%8C%96%E5%B7%A5%E4%B9%8B%E6%97%B6%EF%BC%8C%E4%B9%9F%E6%9C%89%E5%90%84%E7%A7%8D%E4%B8%8D%E5%90%8C%E8%87%AA%E7%84%B6%E6%9D%90%E6%96%99%E4%B8%8E%E6%8A%80%E6%9C%AF%E4%B9%8B%E9%87%8F%E7%94%A8%E4%BA%8E%E5%85%B6%E5%90%88%E6%88%90%E3%80%82
    ###1. Synthesis of natural products as starting materials
    The ancients tasted the genus of plants, trees and flowers to find those containing delicate ingredients, or extracted or distilled to obtain the initial quality. For example, some flowers with specific aromas can be obtained by steam distillation, which may contain ingredients that can be the foundation of synthesis. Take such natural essences, use acid and alkali agents, or apply heat, or catalyze, to make its structure change, and gradually become the required 1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2-7-%E7%A1%9D%E5%9F%BA%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E5%BC%8F%E7%94%A8%E8%87%B3%E5%90%84%E7%A7%8D%E6%96%B9%E9%9D%A2%E3%80%82
    ###2. Chemical reagent construction method
    Although the chemical reagents were not as complete as they are today, the ancients also made good use of what they could get. For example, common salts, such as sodium salts and potassium salts, are combined with active organic reagents. First, the organic reagents undergo a halogenation reaction, and halogen atoms are introduced to increase their reactivity. Then, with the reagents containing nitrogen and oxygen, heat them with fire in a suitable temperature and container, or let them stand in a cool place to make them react slowly. After multi-step transformation, cleverly splice atoms to construct 1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2-7-%E7%A1%9D%E5%9F%BA%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E5%BC%8F%E6%89%80%E9%9C%80%E7%9A%84%E7%BB%93%E6%9E%84%E3%80%82
    ###3. Biosynthesis method
    The ancients also observed the wonders of biology and used them to assist in synthesis. Make certain microorganisms, such as fungi and algae, grow in a special culture medium. When microorganisms grow, they secrete specific enzymes, which have catalytic properties. Input specific substrates, enzymes can make the substrates undergo specific reactions to generate intermediates with specific structures. Supplemented by simple chemical operations, such as separation, purification, and further transformation, you can also obtain 1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2-7-%E7%A1%9D%E5%9F%BA%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E5%BC%8F%E6%89%80%E9%9C%80%E7%9A%84%E7%BB%93%E6%9E%84%E3%80%82
    All these are synthesized by the ancients 1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2-7-%E7%A1%9D%E5%9F%BA%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E5%BC%8F%E4%B9%8B%E8%AF%95%E8%AE%AD%EF%BC%8C%E4%BB%A5%E6%97%B6%E4%B9%8B%E9%97%B4%E4%B9%8B%E5%88%86%E9%87%8F%E5%92%8C%E6%8A%80%E6%9C%AF%E4%B9%8B%E9%99%90%EF%BC%8C%E8%80%8C%E8%83%BD%E6%88%90%E5%88%B0%E4%B9%8B%E7%A8%8B%E5%BA%A6%E4%B9%9F%E5%90%84%E6%9C%89%E4%B8%8D%E5%90%8C%EF%BC%8C%E4%BD%86%E5%88%99%E4%B8%BA%E4%BB%8A%E6%97%B6%E5%88%9B%E6%96%B0%E5%92%8C%E5%85%88%E8%BF%9B%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E5%A4%9A%E6%9C%89%E5%90%84%E7%A7%8D%E5%90%84%E6%A0%B7%E4%B9%8B%E9%87%8F%E3%80%82%E6%9D%A5%E8%87%B4%E5%8F%A4%E4%BB%A3%E5%8C%96%E5%B7%A5%E4%B9%8B%E6%97%B6%EF%BC%8C%E4%B9%9F%E6%9C%89%E5%90%84%E7%A7%8D%E4%B8%8D%E5%90%8C%E8%87%AA%E7%84%B6%E6%9D%90%E6%96%99%E4%B8%8E%E6%8A%80%E6%9C%AF%E4%B9%8B%E9%87%8F%E7%94%A8%E4%BA%8E%E5%85%B6%E5%90%88%E6%88%90%E3%80%82
    ###1. Synthesis of natural products as starting materials
    The ancients tasted the genus of plants and flowers to find those containing delicate ingredients, either by extraction or distillation, to obtain the initial quality. For example, some flowers with specific aromas can be obtained by steam distillation to obtain essential oils, which may contain ingredients that can be the basis for synthesis. Take this kind of natural essence, use acid and alkali agents, or apply heat, or catalyze, to make its structure change, and gradually reach the required 1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2-7-%E7%A1%9D%E5%9F%BA%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E5%BC%8F%E7%94%A8%E8%87%B3%E5%90%84%E7%A7%8D%E6%96%B9%E9%9D%A2%E3%80%82
    ####2. Chemical reagent construction method
    Although the chemical reagents were not as complete as they are today, the ancients also made good use of what they could get. For example, common salts, such as sodium salts and potassium salts, are combined with active organic reagents. First, the organic reagents are halogenated, and halogen atoms are introduced to increase their reactivity. Then, with the reagents containing nitrogen and oxygen, heat them in a suitable temperature and container, or let them stand in a cool place to react slowly. Through multi-step transformation, cleverly splicing atoms to construct 1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2-7-%E7%A1%9D%E5%9F%BA%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E5%BC%8F%E6%89%80%E9%9C%80%E7%9A%84%E7%BB%93%E6%9E%84%E3%80%82
    ###3. Biosynthetic method
    The ancients also observed the wonders of biology and used it to assist in synthesis. Make certain microorganisms, such as fungi and algae, grow in a special medium. When microorganisms grow, they secrete specific enzymes, which have catalytic properties. Input specific substrates, enzymes can make substrates undergo specific reactions to generate intermediates with specific structures. Supplemented by simple chemical operations, such as separation, purification, and further transformation, 1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2-7-%E7%A1%9D%E5%9F%BA%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E5%BC%8F%E6%89%80%E9%9C%80%E7%9A%84%E7%BB%93%E6%9E%84%E3%80%82
    All these were synthesized by the ancients 1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2-7-%E7%A1%9D%E5%9F%BA%E5%96%B9%E5%95%89%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E5%BC%8F%E4%B9%8B%E8%AF%95%E8%AE%AD%EF%BC%8C%E4%BB%A5%E6%97%B6%E4%B9%8B%E9%97%B4%E4%B9%8B%E5%88%86%E9%87%8F%E5%92%8C%E6%8A%80%E6%9C%AF%E4%B9%8B%E9%99%90%EF%BC%8C%E8%80%8C%E8%83%BD%E6%88%90%E5%88%B0%E4%B9%8B%E7%A8%8B%E5%BA%A6%E4%B9%9F%E5%90%84%E6%9C%89%E4%B8%8D%E5%90%8C%EF%BC%8C%E4%BD%86%E5%88%99%E4%B8%BA%E4%BB%8A%E6%97%B6%E5%88%9B%E6%96%B0%E5%92%8C%E5%85%88%E8%BF%9B%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E5%A4%9A%E6%9C%89%E5%90%84%E7%A7%8D%E5%90%84%E6%A0%B7%E4%B9%8B%E9%87%8F%E3%80%82
    What are the precautions for using 1,2,3,4-tetrahydro-7-nitroquinoline?
    1% 2C2% 2C3% 2C4-tetrahydro-7-quinoline boronic acid is a commonly used reagent in organic synthesis. When using it, the following matters should be paid attention to:
    First, it is related to storage conditions. This reagent should be stored in a dry and cool place, away from fire and heat sources. Because it is quite sensitive to humidity, it is prone to moisture and deterioration. If it is damp, it may reduce the reactivity, and even fail to achieve the desired reaction effect. Therefore, it is recommended to use a sealed container when storing, and a desiccant can be added if necessary to maintain its dry environment.
    Second, it involves access operation. When using this reagent, make sure that the utensils used are clean and dry, and avoid the introduction of moisture and impurities. When measuring, when accurately operating, measure according to the amount required for the reaction. If the amount is too much, it will not only cause waste, but also may have adverse effects on the reaction process; if the amount is too small, it will be difficult to achieve the desired reaction, resulting in the failure of the experiment.
    Third, it is related to the control of the reaction conditions. When this reagent participates in the reaction, the reaction temperature, reaction time and the proportion of reactants are all crucial. Under different reaction conditions, its reactivity and selectivity may vary. For example, if the temperature is too high, it may cause side reactions, and if the temperature is too low, the reaction rate will be slow. Therefore, it is necessary to accurately determine the optimal reaction conditions after experimental exploration or based on literature to obtain the ideal reaction results.
    Fourth, safety protection should not be underestimated. During operation, appropriate protective equipment should be worn, such as gloves, goggles, etc. Although its toxicity information may be limited, as an organic reagent, it may still cause irritation to the skin, eyes and respiratory tract. In case of accidental contact, rinse with plenty of water immediately and seek medical treatment according to the actual situation. And after use, the waste should also be properly disposed of, follow relevant environmental regulations, and cannot be discarded at will to avoid polluting the environment.