3 Isoquinolinecarboxamide N 1 1 Dimethylethyl Decahydro
quinoline thiophene imidazole thiazole

3-Isoquinolinecarboxamide, N-(1,1-dimethylethyl)decahydro-

Taiy Chemical

    Specifications

    HS Code

    354307

    Chemical Formula C18H30N2O
    Molar Mass 290.44 g/mol
    Physical State Solid (usually)
    Solubility In Water Low (organic compound, non - polar nature)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Appearance White to off - white powder (commonly)
    Odor Odorless or very faint odor
    Stability Stable under normal conditions, may decompose under extreme heat or in the presence of strong oxidizing agents

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    General Information
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    Frequently Asked Questions

    As a leading 3-Isoquinolinecarboxamide, N-(1,1-dimethylethyl)decahydro- supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    3-Isoquinolinecarboxamide, what is the chemical structure of N- (1,1-dimethylethyl) decahydro-
    This is an investigation into the chemical structure of 3-isoquinoline formamide, N- (1,1-dimethylethyl) decahydro-. Looking at this chemical name, it is composed of many parts. "3-isoquinoline formamide", it can be seen that the main structure is isoquinoline, and there is a formamide group attached at the 3rd position. And "N- (1,1-dimethylethyl) " indicates that the nitrogen atom of the formamide group is connected to 1,1-dimethylethyl. "Decahydro -" reveals that ten hydrogen atoms are added to the benzene ring part of the isoquinoline or the whole heterocyclic system, resulting in a change in its structural saturation. The structure of this compound is complex, and the interaction of various part groups may affect its chemical and physical properties. Its structural characteristics may determine its potential use in organic synthesis, drug research and development and other fields. With chemical rationality, the precise position and connection method of each group is related to the characteristics of this compound. Its structure design is exquisite, and it needs to be deeply analyzed with chemical knowledge to understand its structural mystery.
    What are the physical properties of 3-Isoquinolinecarboxamide, N- (1,1-dimethylethyl) decahydro
    3-Isoquinoline formamide, N - (1,1-dimethylethyl) decahydro - This material has many physical properties. Its appearance may be in a specific form, or in a crystalline state, or in a powder state, which varies depending on the preparation method and environment.
    When it comes to solubility, in common organic solvents, it may exhibit different solubility conditions. In alcoholic solvents, such as ethanol and methanol, it may have a certain solubility and can be mixed with them, but the degree of solubility may vary depending on the solvent characteristics and the proportion of solute. Polar solvents such as water, due to their molecular structure containing hydrophobic groups, may have low solubility, only slightly soluble or even insoluble. The melting point of
    is also an important physical property. When heated to a specific temperature, the intermolecular force changes, and the substance changes from solid to liquid. This melting point may be a key indicator to characterize its purity and structural stability. For materials of different purity, the melting point may be deviated. The higher the purity, the closer the melting point is to the theoretical value. The boiling point of
    is also a key consideration. Under a specific pressure, when heated to the boiling point, the substance changes from liquid to gaseous state. This boiling point value reflects the strength of the intermolecular force. If the force is strong, the boiling point is high; otherwise, it is low.
    Density is also one of the physical properties. The mass of the substance contained in a unit volume can help determine its distribution in the mixture, when mixed with other substances, or stratified according to density differences.
    In addition, the refractive index represents the degree of refraction of light when passing through the substance, which is related to the molecular structure and arrangement. Under specific conditions, it can be used as a means to identify the substance.
    These physical properties are an important basis for in-depth understanding of 3-isoquinolinformamide, N- (1,1-dimethyl ethyl) decahydro -, and are of key value in many fields such as research and application.
    What are the main uses of 3-Isoquinolinecarboxamide, N- (1,1-dimethylethyl) decahydro-
    3-Isoquinolinoformamide, N - (1,1-dimethylethyl) decahydro - This substance has a wide range of uses. In the field of medicine, it may be used as an active ingredient to interact with human biological targets through specific chemical structures to achieve the effect of treating diseases. For example, in the development of drugs for certain diseases, as a key component, it participates in the regulation of human physiological processes and helps to cure diseases. In organic synthetic chemistry, it can act as an important intermediate. With its unique molecular structure, through various chemical reactions, a variety of complex organic compounds can be derived, paving the way for the synthesis of novel materials, fine chemicals, etc. In the field of materials science, it may be used to prepare materials with special properties, such as improving the stability and solubility of materials, and endowing materials with new characteristics to meet the needs of different scenarios. At the level of scientific research and exploration, it provides researchers with important chemical tools to help explore basic scientific issues such as molecular interactions and reaction mechanisms, and to promote the expansion and deepening of knowledge in multidisciplinary fields such as chemistry and biology.
    3-Isoquinolinecarboxamide, N- (1,1-dimethylethyl) decahydro
    To prepare 3-isoquinoline formamide, N - (1,1-dimethylethyl) decahydro -, the following ancient method can be used.
    First take the appropriate starting material, with decahydroisoquinoline as the base, its structure is stable and reactive, which is the key starting structure. In the reactor, add an appropriate amount of decahydroisoquinoline, dissolve it in an organic solvent, so that the raw materials are uniformly dispersed, which is conducive to the reaction. The selected organic solvent must have good solubility and do not side-react with the reactants and products, such as anhydrous ether or tetrahydrofuran.
    Then, slowly add an acylating agent to prepare 3-isoquinoline formamide structure. The acylating reagent should be selected with moderate activity, such as isoquinoline formyl chloride. The addition process needs to be careful and the temperature should be controlled within an appropriate range to prevent overreaction. Generally speaking, the low temperature starts and gradually rises to a suitable reaction temperature, about 0-30 ° C, to ensure the smooth progress of the reaction and generate the target 3-isoquinoline formamide partial structure.
    Then introduce the N - (1,1-dimethylethyl) group, and the tert-butyl reagent can be selected, such as the combination of tert-butyl halide or tert-butyl alcohol and an appropriate catalyst. The reaction conditions at this step are quite important, and alkali substances such as potassium carbonate and sodium carbonate need to be added to promote the reaction. The reaction system is fully reacted at a suitable temperature and time, so that tert-butyl is successfully attached to the nitrogen atom. The temperature is about 40-80 ° C, and the duration varies from time to time. Depending on the reaction progress, thin-layer chromatography or other analytical means are used to monitor.
    After the reaction is completed, the reaction mixture is post-processed. The unreacted reagent is quenched with water first, and then the product is extracted with an organic solvent. After separation, the organic phase is dried with a desiccant to remove water. The organic solvent is removed by rotary evaporation to obtain a crude product.
    The crude product needs to be further purified. The column chromatography method can be used to select an appropriate stationary phase and eluent. According to the polarity difference between the product and the impurity, it can be separated and purified to obtain pure 3-isoquinolinoformamide, N- (1,1-dimethethyl) decahydro-product. The whole process requires fine operation, attention to the control of reaction conditions and post-treatment steps, in order to obtain satisfactory yield and purity.
    3-Isoquinolinecarboxamide, N- (1,1-dimethylethyl) decahydro - what are the precautions during storage and transportation
    3-Isoquinoline formamide, N - (1,1-dimethylethyl) decahydro - Many things should be paid attention to during storage and transportation.
    Bear the brunt, because of its chemical properties, it must be stored in a dry, cool and well-ventilated place. If placed in a humid environment, it may react with water vapor, causing it to deteriorate, affecting quality and utility. At the same time, temperature is also crucial. Excessive temperature may cause changes in its chemical structure, and too low temperature may change its physical state, so it is indispensable to control the appropriate temperature range.
    When transporting, be sure to pack firmly and firmly. It is necessary to choose suitable packaging materials to prevent the package from being damaged in bumps and collisions, resulting in the leakage of the goods. And the means of transportation should also be clean and dry, with no other chemical residues that may react with it. Transport personnel must have a deep understanding of the characteristics of the goods and know the emergency treatment measures. If there is an accident such as leakage during transportation, they should be able to respond quickly and properly to avoid the expansion of the harm.
    In addition, whether it is storage or transportation, relevant laws and standards must be strictly followed. From the specification of the storage place to the formalities and documents of transportation, there must be no slack. Only in this way can we ensure the safety and stability of 3-isoquinoline formamide, N- (1,1-dimethyl ethyl) decahydro-during storage and transportation, and retain its original characteristics and functions to the greatest extent.