N Fmoc D 1 2 3 4 Tetrahydroisoquinoline 3 Carboxylic Acid
quinoline thiophene imidazole thiazole

N-FMOC-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid

Taiy Chemical

    Specifications

    HS Code

    297813

    Chemical Formula C22H21NO4
    Molecular Weight 363.41
    Appearance Solid (usually white or off - white)
    Physical State At Room Temperature Solid
    Solubility In Common Solvents Soluble in organic solvents like dichloromethane, dimethylformamide
    Melting Point Typically in a certain range (specific value depends on purity)
    Chirality D - configuration (has optical activity)
    Functional Groups FMOC group, carboxylic acid group, tetrahydroisoquinoline ring
    Pka Carboxylic Acid Around typical carboxylic acid pKa range
    Uv Vis Absorption Characteristics Absorbs at wavelengths related to its aromatic groups

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    General Information
    Where to Buy N-FMOC-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid in China?
    As a trusted N-FMOC-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading N-FMOC-D-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid 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 structure of N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
    The chemical structure of N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is an important research object in the field of organic chemistry. This compound has a unique structure and contains many key parts.
    The first to bear the brunt is the FMOC group, 9-fluorene methoxycarbonyl, which is like a strong "protective cover". In many organic synthesis reactions, it is often used to protect amino groups from unnecessary reactions during the reaction process and ensure that the reaction occurs precisely at a specific location.
    Furthermore, the D-1,2,3,4-tetrahydroisoquinoline part is a core skeleton with a unique cyclic structure. It is formed by fusing a benzene ring with a nitrogen-containing five-membered heterocyclic ring, and the nitrogen atom and two adjacent carbon atoms together form a partially hydrogenated isoquinoline ring system. This structure endows the compound with a specific spatial configuration and electronic properties, which has a profound impact on its chemical and biological activities.
    Finally, the 3-carboxylic acid group, that is, the carboxyl group (-COOH) at position 3 of the tetrahydroisoquinoline ring. The carboxyl group is acidic and can participate in a variety of chemical reactions, such as ester-forming reactions and amide-forming reactions, which greatly expands the application scope of the compound in the field of organic synthesis. Its existence not only affects the chemical properties of the compound, but also plays a key role in some biological activity studies, or interacts with biological macromolecules such as proteins and enzymes through hydrogen bonding, electrostatic interaction, etc., thus exhibiting unique biological activities.
    In summary, the chemical structure of N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid fuses protective groups, characteristic cyclic skeletons and active functional groups. These parts cooperate to create its important position in the field of organic synthesis and biological activity research.
    What are the main uses of N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
    N - FMOC - D - 1,2,3,4 - tetrahydroisoquinoline - 3 - carboxylic acid, this substance has a wide range of uses. In the field of organic synthesis, it is often used as a key intermediate to help build complex and delicate organic molecular structures. Because of its unique structure, it shines in the field of medicinal chemistry. Many drug research and development are based on this, modified, derived, or can create new drugs with good curative effect and strong specificity, which is of great significance for overcoming difficult diseases.
    In the field of materials science, it also has its own uses. It can be used as a special structural unit to integrate into polymer materials, endowing materials with unique optical, electrical or mechanical properties, and expanding the application boundaries of materials.
    In the field of asymmetric synthesis, due to the existence of chiral centers, they can act as chiral aids or catalysts to guide the reaction to selectively generate products of specific configurations, greatly improve the stereoselectivity and yield of the reaction, and contribute greatly to the acquisition of high-purity chiral compounds.
    This compound has important value in many scientific fields due to its multivariate properties. It is like the key to opening a new journey of scientific research, injecting vitality into the development of various fields, leading the exploration of unknown directions, and driving the wheel of scientific progress forward.
    What are the synthesis methods of N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
    To prepare N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, the method is as follows.
    First take the appropriate starting material, such as isoquinoline derivatives with specific substituents as the base. After multiple steps of delicate transformation, the first step may be to functionalize the specific position of isoquinoline with a specific reagent under mild conditions. This step requires temperature control and time control to achieve accurate substitution.
    In the second step, the unsaturated bond is hydrogenated by a suitable catalytic system to obtain the structure of tetrahydroisoquinoline. In the catalytic reaction, the choice of catalyst and the setting of the reaction atmosphere are all key to maintain the selectivity and efficiency of hydrogenation. < Br >
    Then, the FMOC protecting group is introduced. This process requires the selection of a suitable reaction solvent and base, so that the protecting group can be specifically attached to the target nitrogen atom without affecting other sensitive functional groups in the molecule.
    Finally, under specific conditions, another key check point is carboxylated. The regulation of reaction conditions, such as the equivalent of reagents, reaction temperature and duration, all have a significant impact on the purity and yield of the product. After each step of the reaction, extraction, column chromatography and other separation and purification techniques are required to remove impurities and obtain pure products. After many fine operations, N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is finally obtained.
    What are the precautions for N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid during storage and transportation?
    N - FMOC - D - 1, 2, 3, 4 - tetrahydroisoquinoline - 3 - carboxylic acid In the process of storage and transportation, the following items should be noted:
    First, about storage. Be sure to choose a cool and dry place. If in a humid environment, this compound may change its properties due to moisture erosion, and even undergo chemical reactions, damaging its quality. And the temperature must also be strictly controlled. Excessive temperature can accelerate its decomposition and deterioration. Too low temperature may cause some physical properties to change, so it is generally suitable to store in a specific temperature range, usually 2 - 8 ° C. At the same time, it should be placed separately from oxidizing, reducing and acid-alkaline substances. Due to the relatively active chemical properties of the compound, contact with the above substances is easy to cause a reaction and cause its failure.
    Second, when it comes to transportation. During transportation, the packaging must be solid and stable. Appropriate packaging materials need to be selected to resist vibration, collision, and prevent compound leakage due to package damage. If it is long-distance transportation, special attention should be paid to temperature regulation. Refrigeration equipment or thermal insulation measures can be used to ensure that the temperature during transportation is constant in the appropriate range. And transportation personnel should be familiar with the characteristics of the compound and know the emergency response measures. If there is a leak, it should be dealt with quickly according to the established procedures to prevent the spread of hazards. In short, no matter whether it is storage or transportation, it is necessary to carefully operate to ensure the quality and safety of N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid.
    What is the approximate market price of N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
    I don't know the price of "N-FMOC-D-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid". This is a very professional chemical, and its price is determined for many reasons.
    First, the purchase of materials. If the raw materials required for its preparation are rare and difficult to find, or the cost of obtaining them is high, the price of this chemical must be high. If the ore hidden in the mountains is difficult to mine, using it as a source will make the finished product expensive.
    Second, the method of preparation. If the preparation requires exquisite skills and complex processes, such as the ancient swords, which are tempered in thousands, and consume manpower, material resources, and time, the price is not low. It requires a multi-step reaction, and each step is accurate. If there is a slight error, all previous efforts will be wasted, the cost will increase, and the price will rise.
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    Fourth, the degree of purity. The higher the purity, the more difficult it is to prepare, the more demanding it is, and the more expensive the price will be. Such as pure gold, compared with miscellaneous gold, the price is much higher.
    However, I have not been involved in the market of this chemical, so it is difficult to determine the price. Or ask a chemical market merchant, or ask a scholar who has studied this field carefully, to get an approximate price.