2 N 1 Ethoxycarbonyl 3 Phenylpropyl Alanyl 6 7 Dimethoxy 1 2 3 4 Tetrahydroisoquinoline 3 Carboxylic Acid
quinoline thiophene imidazole thiazole

2-{N-[1-(ethoxycarbonyl)-3-phenylpropyl]alanyl}-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid

Taiy Chemical

    Specifications

    HS Code

    607861

    Chemical Formula C26H32N2O7
    Molecular Weight 484.54 g/mol
    Iupac Name 2-{N-[1-(ethoxycarbonyl)-3-phenylpropyl]alanyl}-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
    Appearance Solid (predicted)
    Boiling Point N/A (predicted)
    Melting Point N/A (predicted)
    Solubility Soluble in organic solvents (predicted)
    Logp 3.2 (predicted)
    Pka N/A (predicted)
    Density N/A (predicted)

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    General Information
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    Frequently Asked Questions

    As a leading 2-{N-[1-(ethoxycarbonyl)-3-phenylpropyl]alanyl}-6,7-dimethoxy-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 2- {N- [1- (ethoxycarbonyl) -3-phenylpropyl] alanyl} -6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid
    This is the name of an organic compound. To know its chemical structure, it needs to be analyzed layer by layer according to the naming rules. "2 - {N - [1 - (ethoxycarbonyl) -3 - phenylpropyl] alanyl} -6,7 - dimethoxy - 1,2,3,4 - tetrahydroisoquinoline - 3 - carboxylic acid", "6,7 - dimethoxy - 1,2,3,4 - tetrahydroisoquinoline - 3 - carboxylic acid" indicates that the main structure is 1,2,3,4 - tetrahydroisoquinoline - 3 - carboxylic acid, and there is a methoxy group attached at positions 6 and 7. " 2 - {N - [1 - (ethoxycarbonyl) -3 - phenylpropyl] alanyl} "is shown at the 2 position of the main structure, connected to a fragment by nitrogen atoms. In this fragment," [1- (ethoxycarbonyl) -3 - phenylpropyl] "indicates that there is an ethoxycarbonyl group at 1 position and a propyl group at 3 positions;" alanyl "is an alanyl group.
    According to this, the chemical structure of the compound is 1, 2, 3, 4-tetrahydroisoquinoline-3-carboxylic acid as the main body, with methoxy groups at positions 6 and 7, and alanyl groups connected to 1-ethoxycarbonyl-3-phenylpropyl groups through nitrogen atoms. Although there is no drawing tool to show an intuitive structure, its general appearance can be imagined after this text description.
    What are the physical properties of 2- {N- [1- (ethoxycarbonyl) -3-phenylpropyl] alanyl} -6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid
    2-% {N- [1- (ethoxycarbonyl) -3-phenylpropyl] alanyl} -6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid, this physical property is very critical, related to its application in various situations.
    First of all, its properties, under room temperature, or white to white powder, fine and uniform texture. Looking at its solubility, in organic solvents, such as ethanol, dichloromethane, etc., there is a certain solubility, but in water, the solubility is relatively low. This difference in solubility is due to the characteristics of functional groups in its molecular structure. The ester groups, carboxyl groups and aromatic rings it contains affect the interaction with different solvent molecules.
    When it comes to the melting point, it is accurately determined to be in a specific temperature range. This melting point data provides an important basis for the identification and purification of the compound. In terms of stability, it is quite stable under normal temperature, normal pressure and dry environment. However, if exposed to high temperature, high humidity, or a specific chemical reagent atmosphere, its structure may change. For example, in a strong acid or alkali environment, ester groups are easy to hydrolyze, causing molecular structure changes, which affects their inherent properties.
    In addition, the spectral characteristics of the compound are also worthy of attention. Its infrared spectrum, at a specific wave number, presents a characteristic absorption peak, corresponding to the vibration of different functional groups. This can be used for structural confirmation and purity analysis. Nuclear magnetic resonance spectroscopy can provide information on the chemical environment of hydrogen and carbon atoms in molecules, helping researchers to clarify their fine structures. These physical properties are like the keys to open the door to the application of this compound, and have important guiding value in the fields of medicinal chemistry and organic synthesis.
    What is the main use of 2- {N- [1- (ethoxycarbonyl) -3-phenylpropyl] alanyl} -6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid
    2-% {N- [1- (ethoxycarbonyl) -3-phenylpropyl] alanyl} -6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid, this is an organic compound. Looking at the complexity of its structure, it may have extraordinary uses in the field of medicinal chemistry.
    In the past, Shennong tasted all kinds of herbs to explore the properties of herbs and lay the foundation for future medicine. Today's organic synthesis is also the way to explore fairy grass. This compound may be synthesized artificially and skillfully, and its fine structure must contain unique pharmacology.
    In drug development, it may be a key intermediate. Because of its special structure, it may be able to precisely fit with specific targets in the body. Like the good general of ancient times, it can directly attack Huanglong and adjust the biochemical balance of the human body. Or it can participate in the construction of active drug molecules, just like masonry is indispensable in tall buildings.
    Furthermore, in the study of organic chemistry, this compound can be used as a research object to study the reaction mechanism and explore new synthesis paths. Its structure is complex, such as the wonder of a maze. Research can expand the boundaries of chemical cognition. If the ancient sages explore the secrets and expand the boundaries of knowledge.
    Or occasionally involved in material science, although it is not its main use, but the wonders of science often lead to accidents. Like the treasures of ancient times, in different situations, or have different functions. Although it is not clear, there may be new ways to explore.
    What are the synthesis methods of 2- {N- [1- (ethoxycarbonyl) -3-phenylpropyl] alanyl} -6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid
    2-% {N- [1- (ethoxycarbonyl) -3-phenylpropyl] alanyl} -6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid is a complex organic compound, and its synthesis method is quite exquisite.
    To synthesize this product, you can follow the following steps. The first step is to prepare the key intermediate. With suitable starting materials, through a series of reactions, such as nucleophilic substitution, esterification, etc., 1- (ethoxycarbonyl) -3-phenylpropyl fragment is prepared. The preparation of this fragment requires the selection of appropriate reaction conditions and reagents, such as selecting suitable halogenated hydrocarbons and alcohols, and performing esterification under the catalysis of bases to obtain pure 1- (ethoxycarbonyl) -3-phenylpropyl intermediates. < Br >
    The second step is to construct the alanyl-related structure. Alanine can be used to protect one of the amino and carboxyl groups through an appropriate protection group strategy, and then condensate with the aforementioned intermediates. For example, the amino group of alanine is first protected by a protective group such as Boc, so that its carboxyl group and 1- (ethoxycarbonyl) -3-phenylpropyl fragment are condensed under the action of a condensing agent such as DCC (dicyclohexyl carbodiimide) to form an amide bond, and then the protective group is removed to obtain a product containing the target fragment.
    Furthermore, 6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid part. The corresponding aromatic compound can be used to introduce the methoxy group through the methoxylation reaction, and then the isoquinoline ring can be constructed through the cyclization reaction, and then the carboxyl group can be introduced. For example, using catechol as the starting material, react with dimethyl sulfate under the action of base, introduce the methoxy group, and then undergo a multi-step reaction, including condensation cyclization with a suitable nitrogen-containing compound, and finally introduce the carboxyl group through oxidation or other suitable reactions.
    Finally, the alanyl-containing fragment is connected to the 6,7-dimethyl-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid part through a condensation reaction. During this process, the reaction conditions, such as temperature, pH value, etc., need to be carefully regulated to ensure that the reaction proceeds in the direction of the formation of the target product and avoid the occurrence of side reactions. Through this series of reactions, 2-% {N- [1- (ethoxycarbonyl) -3-phenylpropyl] alanyl} -6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid can be successfully synthesized. After each step of reaction, separation and purification methods are required, such as column chromatography, recrystallization, etc., to obtain high-purity products to ensure the success of synthesis.
    What is the market outlook for 2- {N- [1- (ethoxycarbonyl) -3-phenylpropyl] alanyl} -6,7-dimethoxy-1,2,3, 4-tetrahydroisoquinoline-3-carboxylic acid
    Today there is a product called 2 - {N - [1 - (ethoxycarbonyl) -3 - phenylpropyl] alanyl} -6,7 - dimethoxy - 1,2,3,4 - tetrahydroisoquinoline - 3 - carboxylic acid. This is an organic compound, which may have potential research value in the field of pharmaceutical chemistry.
    Looking at its market prospects, this compound may have a place in the scientific research reagent market. When researchers explore the mechanism of drug action and develop new drugs, they may need this as a tool for experimental research, so there may be a stable demand for scientific research reagent suppliers.
    However, its industrial production may pose challenges. The process of synthesizing this compound may involve multi-step reactions, with severe conditions and high requirements for reaction equipment and technology. And raw material acquisition and cost control are all difficult problems. If large-scale industrial production is to be achieved, the synthesis route must be optimized, costs reduced and efficiency increased, and the market supply can be expanded.
    In the field of drug research and development, if its biological activity and pharmacological effects can be confirmed, it may become a lead compound, which can be modified and optimized into a new drug. However, the road to new drug development is long, and it requires a lot of experiments and strict approval, which is quite risky.
    Overall, 2 - {N - [1 - (ethoxycarbonyl) -3 - phenylpropyl] alanyl} -6,7 - dimethoxy - 1,2,3,4 - tetrahydroisoquinoline - 3 - carboxylic acid has potential value, but to open up a broad market prospect, it is necessary to cooperate with scientific research and industry to overcome technical and cost difficulties.