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

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

Taiy Chemical

    Specifications

    HS Code

    241550

    Name N-FMOC-L-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid
    Chemical Formula C25H21NO4
    Molecular Weight 399.44 g/mol
    Appearance Solid (usually white to off - white)
    Solubility Soluble in organic solvents like DMF, DMSO
    Chirality Chiral, L - configuration
    Pka Carboxylic acid pKa around 3 - 5 (estimated for the COOH group)
    Boiling Point Decomposes before boiling (due to instability at high temperatures)
    Melting Point 160 - 165 °C (approximate)
    Storage Conditions Store in a cool, dry place, protected from light

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    General Information
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    Frequently Asked Questions

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    What is the chemical structure of N-FMOC-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
    The full Chinese name of this compound is N-fluorene methoxycarbonyl-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid. To clarify its chemical structure, let me explain in detail.
    This compound uses L-1,2,3,4-tetrahydroisoquinoline as the basic skeleton. Tetrahydroisoquinoline is formed by fusing a benzene ring with a nitrogen-containing five-membered heterocyclic ring, and the nitrogen atom is directly connected to the benzene ring, and four hydrogen atoms are added at the 1, 2, 3, and 4 positions to form a saturated state.
    There is a carboxyl group (-COOH) at the 3 position, which gives the compound acidic characteristics and can participate in various acid-base reactions, esters, amides and other reactions.
    And N-fluorene methoxycarbonyl (Fmoc) is attached to the nitrogen atom. The Fmoc structure contains a fluorene group, which is connected to the carbonyl group (-C = O) through methylene (-CH 2O -), and the carbonyl group is then connected to the nitrogen atom. The fluorene group is formed by fusing two phenyl rings with a five-membered ring. The Fmoc group is often used as a protective group for the amino group. In reactions such as peptide synthesis, it can effectively protect the amino group and avoid unnecessary side reactions during the reaction. It can be removed at an appropriate time to restore the activity of the amino group and continue to participate in the reaction. In this way, the chemical structure of N-fluorene methoxycarbonyl-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is clearly presented.
    What are the main uses of N-FMOC-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
    N-FMOC-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is a key compound in the field of organic synthesis and medicinal chemistry. It has a wide range of uses and plays a significant role in many important fields.
    is the first to bear the brunt. In the field of drug research and development, this compound can be used as a key intermediate due to its unique chemical structure. Many biologically active drug molecules often rely on this compound as the starting material or key module in the synthesis process. Through ingenious modification and derivatization of its structure, new compounds with diverse pharmacological activities can be constructed, such as the development of anti-cancer, antibacterial, antiviral and other drugs.
    Furthermore, in the field of organic synthesis chemistry, N-FMOC-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid is an important synthetic building block. Because it contains specific functional groups, it can participate in many types of organic reactions, such as acylation reactions, alkylation reactions, and cyclization reactions. Through these reactions, chemists can construct complex and novel organic molecules, which greatly enrich the variety of organic compounds and contribute to the development of organic synthesis chemistry.
    In addition, in the field of materials science, this compound may be introduced into polymer materials by specific means to endow materials with unique properties. It can improve the biocompatibility, optical properties or electrical properties of materials, so as to expand the application of materials in biomedical materials, optoelectronic materials and other fields.
    In short, N-FMOC-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid plays an indispensable role in drug development, organic synthetic chemistry and materials science, and is of great significance to promote progress in related fields.
    What are the synthesis methods of N-FMOC-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
    To prepare N-FMOC-L-1, 2, 3, 4-tetrahydroisoquinoline-3-carboxylic acid, there are various methods. The ancient method of synthesizing compounds is often selected according to the properties of the substance and the materials it has.
    First, or by a suitable starting material, through a condensation reaction, the molecular structure is initially formed. For example, based on a compound with a specific functional group, by the force of a condensing agent, it is connected to each other to gradually build the required tetrahydroisoquinoline skeleton. This process requires attention to the reaction conditions, and temperature and solvent can affect its formation. If the temperature is high, the reaction speed may be affected, but there may be side reactions; if the temperature is low, the speed may be slower, and the product may be purer. < Br >
    Second, the method of catalysis is also commonly used. Choose the right catalyst, which can promote the reaction, and has specificity, so that the reaction is in the desired direction. For example, in the reaction of metal catalysis, the characteristics of metals can be used to activate specific bonds and guide the direction of the reaction. However, the choice of catalyst is very important, and its activity and stability are all related to the success or failure of the reaction.
    Third, the strategy of protecting the group is also important. In the reaction, in order to prevent a specific functional group from being affected, it is often covered by a protective group. After the reaction is completed, the protective group is removed to obtain a pure product. For example, the FMOC group can protect the amino group, so that it is not disturbed by other substances in the reaction. When it is completely reacted, it can be properly removed.
    In short, to synthesize this compound, it is necessary to consider the application of raw materials, reaction conditions, catalysts and protective bases, and to obtain the desired product.
    What are the physicochemical properties of N-FMOC-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid?
    N - FMOC - L - 1,2,3,4 - tetrahydroisoquinoline - 3 - carboxylic acid is an important compound in organic synthesis. The physical and chemical properties of this substance are unique and have a profound impact on its performance in various chemical reactions and application fields.
    When it comes to physical properties, its properties are usually solid, and its color may be white to off-white. Melting point is also a key physical parameter, and specific melting point values can help identify and determine purity. Generally speaking, its melting point is in a certain temperature range, which varies slightly depending on the purity and crystalline morphology of the compound.
    At the level of chemical properties, the FMOC group in the molecule has a good protective effect and can be easily removed under specific reaction conditions, so that the carboxylic acid group can participate in various reactions. The structural part of L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid endows the molecule with unique reactivity. Its carboxylic acid groups can undergo common carboxylic acid reactions such as esterification and amidation, and are used in the field of organic synthesis to construct a variety of compound structures.
    In addition, the solubility of the compound is also an important property. In common organic solvents, such as dichloromethane, N, N-dimethylformamide, etc., it has a certain solubility, which provides convenience for its application in solution-phase reactions. The solubility in water is relatively low, and this difference can be exploited during separation and purification.
    What is the price range of N-FMOC-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid in the market?
    I don't know the price of "N-FMOC-L-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid" in the market. However, in order to estimate its price, various factors need to be considered.
    First, it is difficult to prepare this substance. If the synthesis method is complicated, the materials used are rare, and exquisite craftsmanship and harsh conditions are required, the price will be high. Such as the ancient alchemy, seeking the medicine of longevity, the materials used are precious, the process is complicated, and the price of the finished medicine is comparable.
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    Third, the quality is high or low. Those with high quality are like flawless jade, and the price is not cheap; while those with poor quality, such as the genus of rubble, the price must be low.
    Fourth, the difference in origin. In different places, the price is also different due to differences in raw materials, manpower, taxes, etc.
    "N - FMOC - L - 1,2,3,4 - tetrahydroisoquinoline - 3 - carboxylic acid" in the market today. Without detailed information, it is difficult to determine its price. Or for high-end scientific research purposes, the quality is excellent, and the price is as high as a thousand gold; or it is commonly prepared, the quantity is large and the quality is average, and the price is close to the people. It is necessary to carefully check the market conditions and the manufacturer's quotation to know the range of its exact price.