2 3 Dihydro 1h Benz De Isoquinoline
quinoline thiophene imidazole thiazole

2,3-Dihydro-1H-benz[de]isoquinoline

Taiy Chemical

    Specifications

    HS Code

    497789

    Chemical Formula C13H11N
    Molecular Weight 181.23 g/mol
    Appearance Solid (usually)
    Physical State At Room Temp Solid
    Melting Point Data may vary, needs specific determination
    Boiling Point Data may vary, needs specific determination
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane
    Odor Typically odorless or very faint odor
    Density Data may vary, needs specific determination
    Pka Data may vary, needs specific determination
    Uv Absorption Absorbs in certain UV wavelengths characteristic of aromatic systems

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    General Information
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    Frequently Asked Questions

    As a leading 2,3-Dihydro-1H-benz[de]isoquinoline 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 2,3-dihydro-1H-benzo [de] isoquinoline?
    2% 2C3 -diethyl- 1H -indolo [de] quinoline is a special chemical compound, and its physical properties are not worth exploring.
    This compound is often solid, and under normal conditions, it is mostly shown in the appearance of crystals. Its melting is one of the important physical studies, and it has been investigated for a long time, probably to a certain extent. This melting property is very important for the production of chemical compounds. If you want to extract this substance, you can rely on its melting, by re-crystallization, etc., to make the effective separation of the chemical.
    Furthermore, its solubility cannot be ignored. In soluble systems, such as certain alcohols and ethers, they may have a certain solubility. In water, the solubility is limited. This solubility property is important for both the synthesis of antibodies and the separation of antibodies. If the reaction is to be performed in a homogeneous system, it is necessary to select the appropriate solubility of the compound that can dissolve the compound.
    In addition, the density of 2% 2C3-di- 1H-indolo [de] quinoline is also one of its physical properties. The density of the fixed phase is low, but it is not important for the compound in some processes involving density phases, such as liquid-liquid extraction. Knowing its density, in order to more precisely control the operation of the phase, improve the efficiency of the work and improve the quality of the material.
    Its external characteristics are also an important factor in identifying the material, usually white to white solid color. In addition, in the preliminary determination of the compound, it can provide direct information. In addition, the general physical properties of this compound, mutual, together become the physical properties of its characteristics, which are indispensable for chemical research and related engineering applications.
    What are the chemical properties of 2,3-dihydro-1H-benzo [de] isoquinoline
    2% 2C3 -dihydro-1H -indolo [de] isoquinoline This compound has multiple chemical properties. It contains unsaturated bonds, so it has the property of addition. In case of hydrogen, under suitable catalysts and conditions, unsaturated bonds can be added to hydrogen, resulting in structural saturation changes and different properties.
    Because of its nitrogen heterocyclic ring, it is alkaline to a certain extent. The lone pair electrons on the nitrogen atom can bind protons and can form salts in acidic environments. This property changes its solubility and other physical properties, and can be used for separation and purification.
    In addition, the ring system of the compound is conjugated, which has certain stability, and because of the conjugated structure, it has special spectral properties. In the ultraviolet-visible spectrum, specific absorption peaks can be found, depending on the peak position and intensity, and structural characteristics can be inferred for qualitative and quantitative analysis.
    And because it has active hydrogen, or can participate in the substitution reaction. Under appropriate reagents and conditions, active hydrogen can be replaced by other groups, and various compounds can be derived. It is widely used in the field of organic synthesis and can provide a basis for the creation of new drugs and materials. In short, 2% 2C3-dihydro-1H-indolo [de] isoquinoline is of great significance in many fields of chemistry due to its unique structure and rich chemical properties.
    What are the main uses of 2,3-dihydro-1H-benzo [de] isoquinoline?
    2% 2C3-dihydro-1H-indolo [de] isoquinoline is a class of organic compounds. Its main uses are quite wide, and it is often a key intermediate for the creation of new drugs in the field of medicinal chemistry. Due to its unique chemical structure, it has the potential to interact with specific targets in organisms, so it can be used to develop drugs with specific pharmacological activities, such as anti-tumor, anti-viral, and anti-nervous system diseases.
    In the field of materials science, it also has its uses. Or it can be modified and assembled to prepare materials with special optical and electrical properties, such as used in organic Light Emitting Diodes (OLEDs), solar cells and other devices, to improve the photoelectric conversion efficiency and stability of materials by their structural properties.
    Furthermore, in the field of organic synthetic chemistry, this compound is an important cornerstone for the construction of more complex organic molecules. Chemists can use a variety of organic reactions to derive their structures, expand the structural diversity of compounds, and then explore novel reaction paths and synthesis strategies to promote the development of organic synthetic chemistry. In conclusion, 2% 2C3 -dihydro-1H -indolo [de] isoquinoline has important uses in many scientific fields, providing many possibilities for scientific research and industrial applications.
    What are the synthesis methods of 2,3-dihydro-1H-benzo [de] isoquinoline
    The synthesis method of Fu 2,3-dihydro-1H-benzo [de] isoquinoline has been studied extensively, and there are various paths to follow.
    One is formed by nucleophilic substitution reaction. First take an appropriate halogenated aromatic hydrocarbon and make it interact with a nucleophilic nitrogen-containing reagent. Under suitable reaction conditions, if a suitable solvent is selected and an appropriate temperature and pressure are controlled, the halogen atom can be replaced by the nitrogen atom, and the basic structure of benzo [de] isoquinoline can be gradually established. In this process, the polarity of the solvent and the temperature of the reaction have a significant impact on the reaction rate and the selectivity of the product.
    The second can be achieved by cyclization reaction. Starting with a specific chain-like precursor compound, the cyclic structure of benzo [de] isoquinoline is constructed through the cyclic reaction in the molecule. In this case, it may be necessary to use the force of the catalyst to catalyze the rearrangement and condensation reactions in the molecule to promote the smooth progress of cyclization. The type and dosage of the catalyst need to be finely regulated to obtain the ideal yield and purity.
    Furthermore, the synthesis method of transition metal catalysis has also attracted much attention. The unique catalytic properties of transition metals are used to activate the substrate molecules and promote the formation of carbon-nitrogen bonds and carbon-carbon bonds. This method has the advantages of high efficiency and good selectivity. However, the cost, recovery and reuse of transition metal catalysts also need to be considered in order to achieve a balance between economy and environmental protection.
    There is also a method of bionic synthesis. Simulate the chemical reaction mechanism in organisms, and realize the synthesis of 2,3-dihydro-1H-benzo [de] isoquinoline under mild reaction conditions. This path often requires in-depth exploration of the enzyme catalysis process in organisms, and artificial synthesis to simulate its catalytic active center, so as to achieve the synthesis of the target product, which is expected to open up a novel and green way for the synthesis of this compound.
    What is the price range of 2,3-dihydro-1H-benzo [de] isoquinoline in the market?
    I think what you are asking is about the price range of 2,3-dihydro-1H-indolo [de] isoquinoline in the market. However, this compound is not familiar to me, and it is difficult to find a detailed description of its price in ancient books.
    In the modern market, the price of various compounds often varies for many reasons. First, the difficulty of preparation is the key. If the synthesis of this product is complicated and requires exquisite skills and rare raw materials, the price will be high. Second, the amount of demand also affects the price. If it is needed by many industries, there are many users, and the supply is in short supply, and the price will rise; if there is a lack of demand, the price may drop. Third, the price of the raw materials also has an impact. If the raw materials required for the preparation of this product are expensive and difficult to obtain, the price of the finished product will also rise accordingly.
    I'm sorry I don't have the exact number to tell you the price range. If you want to know, you can go to the pharmaceutical market, the place where the chemical raw materials are traded, and consult various merchants; or on the Internet, find the platform where the chemical products are traded, and check the price, and you can get an approximate amount. I hope you will get what you want, and you can solve the confusion in your heart.