1 2 3 4 Tetrahydro 6 Methoxy 1 Isoquinolinecarbonitrile
quinoline thiophene imidazole thiazole

1,2,3,4-tetrahydro-6-methoxy-1-isoquinolinecarbonitrile

Taiy Chemical

    Specifications

    HS Code

    563067

    Chemical Formula C11H12N2O
    Molar Mass 188.226 g/mol

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    General Information
    Where to Buy 1,2,3,4-tetrahydro-6-methoxy-1-isoquinolinecarbonitrile in China?
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    Frequently Asked Questions

    As a leading 1,2,3,4-tetrahydro-6-methoxy-1-isoquinolinecarbonitrile 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 chemical properties of 1,2,3,4-tetrahydro-6-methoxy-1-isoquinoline formonitrile?
    1% 2C2% 2C3% 2C4-tetrahydro-6-methoxy-1-isopropenylbenzaldehyde, which is an organic compound with the following chemical properties:
    1. ** Properties of aldehyde groups **: Containing aldehyde groups, with typical aldehyde chemical properties. Oxidation reaction can occur. Under the action of weak oxidants such as Torun reagent (silver ammonia solution), the aldehyde group is oxidized to a carboxyl group, and silver is precipitated at the same time. This is the silver mirror reaction. The reaction formula is: R - CHO + 2Ag (NH < unk >) - OH → R - COONH < unk > + 2Ag < unk > + 3NH < unk > + H < unk > O (where R removes the residual part of the aldehyde group for this compound); Reacted with Feilin reagent, the aldehyde group reduces copper hydroxide to cuprous oxide brick red precipitation, which can be used for aldehyde group qualitative inspection. Reduction reaction can also occur, using hydrogen as a reducing agent, under the action of catalyst, the aldehyde group can be reduced to alcohol hydroxyl group to generate corresponding alcohol compound.
    2. ** Properties of alkenyl groups **: Contains isopropylene groups, with olefin properties. Addition reactions can occur, such as addition with bromine water, bromine atoms in the bromine elemental substance are added to the carbon atoms at both ends of the carbon-carbon double bond to fade the bromine water. The reaction formula is: R - CH = CH _ + Br _ → R - CHBr - CH _ Br (R removes the remainder of the isopropylene group for this compound); addition reactions can also occur with hydrogen, hydrogen halide, etc. Under certain conditions, the isopropylene group can undergo polymerization to form a polymer.
    3. ** Properties of alkoxy groups **: The 6 position contains methoxy groups, which are relatively stable, but some reactions can occur under specific conditions. For example, under the action of strong acids, ether bonds may be broken to form corresponding phenols and halogenated hydrocarbons or alcohols.
    4. ** Properties of benzene rings **: Molecules contain benzene rings and are aromatic. Electrophilic substitution reactions can occur, such as halogenation reactions, which react with halogen elements under the catalysis of iron or iron salts, and halogen atoms replace hydrogen atoms on the benzene ring; nitrification reactions, in the mixed acid of concentrated sulfuric acid and concentrated nitric acid, nitro groups are introduced on the benzene ring; sulfonation reactions, which react with concentrated sulfuric acid, introduce sulfonic acid groups on the benzene ring.
    What is the synthesis method of 1,2,3,4-tetrahydro-6-methoxy-1-isoquinoline formonitrile?
    To prepare 1% 2C2% 2C3% 2C4-tetrahydro-6-methoxy-1-isopropenyl naphthalene, the method is as follows:
    First take an appropriate amount of starting materials, carefully weigh them, and place them in a clean reactor. Specific temperature and pressure conditions must be maintained in the kettle. These two are the key elements of the reaction. A slight difference may cause reaction errors. Usually the temperature should be controlled in a certain precise range, and the pressure should also meet the established standards.
    Then, slowly add a specific catalyst. This catalyst is the "guide" of the reaction, which can effectively promote the progress of the reaction and change the rate of the chemical reaction. The dosage needs to be strictly determined according to the formula. Most may initiate side reactions, and at least the reaction may be difficult to fully advance.
    During the reaction process, continuous and close monitoring is required. With advanced analytical instruments, such as high-performance liquid chromatography, etc., real-time insight into the degree of reaction and the purity of the product can be obtained. According to the monitoring results, fine-tune the reaction conditions, such as temperature, pressure, and addition rate of reactants, etc., to ensure that the reaction proceeds along the expected path.
    After the reaction is approaching completion and the product is initially present, it needs to go through a series of separation and purification steps. This step is designed to remove impurities in the product and improve the purity of the product. Classical separation methods such as extraction, distillation, and recrystallization can be used for multiple treatments until the purity of the product reaches the required standard.
    The entire synthesis process has strict requirements on the quality of raw materials, reaction conditions, and operating techniques. Each step needs to be carefully controlled to successfully prepare 1% 2C2% 2C3% 2C4-tetrahydro-6-methoxy-1-isopropylnaphthalene. A slight omission may affect the quality and yield of the product.
    In what fields is 1,2,3,4-tetrahydro-6-methoxy-1-isoquinolinoformonitrile used?
    1% 2C2% 2C3% 2C4-tetrahydro-6-methoxy-1-isopropylbenzene, an organic compound. It has applications in many fields.
    In the field of medicine, or involved in drug research and development. Because of its unique chemical structure, or can exhibit specific biological activities, it can be used as a lead compound to help researchers create new drugs for disease treatment. For example, it may have affinity for specific disease targets and be optimized into effective therapeutic drugs.
    In the fragrance industry, or it is used because of its special smell. Or it provides a unique flavor for blending fragrances, adding aroma layering and uniqueness. In the fragrance formula of perfumes, air fresheners, detergents and other products, it may contribute a unique fragrance and enhance the olfactory experience of the product.
    In the field of organic synthesis, it can be used as a key intermediate. With its functional group characteristics, it participates in various organic reactions and builds more complex organic molecular structures. Organic synthesis chemists can use it to expand the structural diversity of compounds, synthesize organic compounds with special functions or properties, and provide basic raw materials for materials science, chemical research, etc.
    In the field of materials science, or chemically modified to give materials special properties. For example, the introduction of specific material systems to improve material solubility, stability, optical properties, etc., provides the possibility for the development of new functional materials.
    What are the market prospects for 1,2,3,4-tetrahydro-6-methoxy-1-isoquinoline formonitrile?
    1% 2C2% 2C3% 2C4-tetrahydro-6-methoxy-1-isopropylacetophenone, this is an organic compound. Looking at its market prospects, it can be said that opportunities and challenges coexist.
    From the demand side, in the field of medicine, it may be a key intermediate and can participate in the synthesis of many specific drugs. Nowadays, people pay more and more attention to health, the pharmaceutical market continues to expand, and the demand for characteristic APIs is increasing. If the efficacy of the drug involved in this compound is certain, the market demand for it may rise steadily. In the fragrance industry, due to its unique chemical structure, or giving products a different aroma, with people's rising demand for high-quality fragrances, it may have a chance to emerge in the fragrance field.
    However, looking at the supply side, there may be technical barriers to synthesizing this compound. If the synthesis process is complex and the reaction conditions are strict, the production cost will remain high, restricting its large-scale production, thereby affecting the market supply. And the chemical industry has stricter environmental protection requirements. If a large number of pollutants are generated in the production process, enterprises need to invest huge amounts of environmental protection funds to meet compliance requirements, increase operating costs, and weaken the market competitiveness of products.
    Furthermore, market competition should not be underestimated. If many companies in the industry covet this field and lay out production one after another, the market may be oversupplied, triggering a price war and compressing profit margins.
    In summary, 1% 2C2% 2C3% 2C4-tetrahydro-6-methoxy-1-isopropylacetophenone Although the market prospect is bright, the road ahead is also full of thorns. Practitioners need to gain insight into market dynamics, break through technical bottlenecks, and strictly abide by environmental protection red lines in order to gain a place in the market.
    Is the production process of 1,2,3,4-tetrahydro-6-methoxy-1-isoquinolinoformonitrile complicated?
    The production process of 1% 2C2% 2C3% 2C4-tetrahydro-6-methoxy-1-isopropylphenylacetic acid is not simple and complicated.
    The synthesis of this compound involves the selection and pretreatment of raw materials first. The selected raw materials need to be of high purity and have some impurities, which may cause reaction deviations and affect the quality of the product. The pretreatment process, or the steps involving purification and drying, all need to be carefully controlled. If there is a slight difference, the root cause may be planted.
    The reaction process is particularly critical. The setting of reaction conditions, such as temperature, pressure, and catalyst dosage, all need to be precisely controlled. If the temperature is too high, it may cause frequent side reactions and reduce the purity of the product; if the temperature is too low, the reaction rate will be slow and take a long time. The same is true for pressure, or a specific range may be required to prompt the reaction to proceed in the desired direction. The catalyst is like a guide to the reaction. If the dosage is appropriate, it can accelerate the reaction; if the dosage is inappropriate, it may cause the reaction to go out of control.
    The monitoring of the reaction process cannot be ignored. It is necessary to use high performance liquid chromatography, mass spectrometry and other analysis methods to gain real-time insight into the reaction progress, so as to adjust the reaction conditions in time and ensure that the reaction proceeds according to the established path.
    The separation and purification of the product is also a difficult challenge. At the end of the reaction, the product is often mixed in impurities. To obtain a high-purity product, it needs to go through multiple separation processes, such as extraction, distillation, recrystallization, etc. Each process operation requires caution. If there is a little carelessness, the product may be lost, or the purity may not reach the standard.
    In the post-processing stage, the stability of the product and storage conditions also need to be fully considered. A little negligence, the product may deteriorate, and all previous efforts will be wasted.
    In summary, the production process of 1% 2C2% 2C3% 2C4-tetrahydro-6-methoxy-1-isopropylphenylacetic acid, from raw materials to finished products, is dangerous every step of the way, and refinement is required everywhere. It is a complex and abnormal project.