S 1 2 3 4 Tetrahydro 3 Isoquinolinecarboxylic Acid
quinoline thiophene imidazole thiazole

S-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid

Taiy Chemical

    Specifications

    HS Code

    951556

    Name S-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic acid
    Chemical Formula C10H11NO2
    Molar Mass 177.20 g/mol
    Appearance Solid (usually white or off - white)
    Solubility In Water Moderate solubility
    Melting Point 140 - 145 °C (approximate, may vary with purity)
    Pka Value Related to the carboxylic acid group, around 4 - 5
    Chirality It has a chiral center at the S - configured carbon
    Boiling Point Decomposes before boiling due to heat - sensitive nature
    Density Estimated around 1.2 - 1.3 g/cm³

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    Frequently Asked Questions

    As a leading S-1,2,3,4-Tetrahydro-3-isoquinolinecarboxylic 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 S-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid?
    The chemical structure of S-1,2,3,4-tetraamine-3-isopentenyl cinnamic acid is a complex and interesting problem in the field of organic chemistry. The analysis of the structure of this compound depends on the basic principles of organic chemistry and various analytical methods.
    Looking at its name, "S-1,2,3,4-tetraamine", it can be seen that there is a nitrogen-containing part of its molecule with a specific configuration. "Amine" refers to the functional group of the nitrogen atom connected to the hydrogen atom or hydrocarbon group. Here, the four amine groups are arranged in a specific spatial configuration (S configuration, a specific stereochemical structure of the usual chiral center), which has a great influence on the physical and chemical properties of the compound.
    "3-isopentenyl cinnamic acid", "cinnamic acid" is an organic acid with the structure of benzene ring and acrylic acid. In its structure, the benzene ring imparts certain stability and aromaticity to the compound, while the acrylic part is reactive and can participate in many addition, esterification and other reactions. And "3-isopentenyl group" is the substituent connected to the third position in the cinnamic acid structure. Isopentenyl has a carbon-carbon double bond, which not only increases the unsaturation of the molecule, but also affects the electron cloud distribution and reactivity of the whole molecule due to the conjugation effect.
    From a comprehensive perspective, the chemical structure of S-1,2,3,4-tetraamine-3-isopentenyl cinnamic acid is composed of the tetraamine part with a specific three-dimensional configuration connected to the cinnamic acid part containing isopentenyl substitution. This complex structure endows the compound with unique physical and chemical properties, which may have potential application value in the fields of medicinal chemistry and total synthesis of natural products. However, to accurately determine its structure, modern analytical techniques such as nuclear magnetic resonance (NMR), mass spectrometry (MS), and infrared spectroscopy (IR) are needed to confirm the connection order, spatial configuration, and functional group characteristics of each atom.
    What are the physical properties of S-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid?
    The physical properties of S-1,2,3,4-tetraammonia-3-isopentenyl cinnamic acid are quite unique. At room temperature, this compound is often in the form of a solid state, and its texture is relatively solid. Its color is either white or yellowish, just like the light of light gold in the first snow, pure and unique.
    When it comes to solubility, the degree of solubility of this substance in water is low, like a lone boat that cannot be melted in the vast sea. However, among organic solvents, such as ethanol and acetone, it can show good solubility, just like fish getting water and blending leisurely. This property is due to the specific interaction between the groups contained in its molecular structure and the organic solvent molecules, which makes the two able to affinity each other.
    Its melting point is also a significant physical property. After fine determination, its melting point is within a certain range, which provides an important basis for identifying the compound. When the temperature gradually rises to the melting point, the substance will slowly transform from a solid state to a liquid state, just like ice and snow melting gradually when warm. During this process, the arrangement and interaction between molecules undergo subtle changes, from an ordered solid lattice structure to a relatively disordered liquid structure.
    In addition, the density of this compound is also one of its important physical properties. Its density is specific, which is unique compared with common substances. This density value reflects the density of molecules in a unit volume, and is also closely related to the size, mass and arrangement of molecules. This physical property is of great significance for judging the purity of the compound and preparing specific dosage forms in practical applications and research.
    What are the main uses of S-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid?
    S-1,2,3,4-tetraamine-3-isopentenyl flavonoid acid, this substance is of great benefit to medicine. It can be used as medicine and has extraordinary effects in regulating qi and blood in human organs and resisting various diseases.
    First, in the way of anti-tumor, this substance can inhibit the growth and proliferation of tumor cells, just like a magic weapon strangling the throat where tumors are raging. Or by regulating related signaling pathways, the pace of division of tumor cells is blocked and gradually apoptosis. This is a powerful helping hand in the fight against cancer and brings hope of recovery to countless people entangled by diseases.
    Second, in the prevention and treatment of cardiovascular diseases, it has also shown its presence. It can regulate blood lipids, balance the lipid components in the blood, reduce blood viscosity, like dredging a river, making blood flow smoother and reducing the risk of thrombosis. At the same time, it also has the function of protecting vascular endothelial cells, strengthening the barrier of blood vessels, maintaining the normal physiological function of blood vessels, and protecting the health of the cardiovascular system.
    Third, it is also unique in neurological diseases. It can enhance the activity of nerve cells and enhance their ability to resist damage, like a layer of armor for nerve cells. For neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease, it can delay the progression of the disease, improve the cognitive and motor functions of patients, and give patients hope for life.
    Fourth, the anti-inflammatory effect should not be underestimated. It can inhibit the release of inflammatory factors, reduce the body's inflammatory response, and seem to be a good general to calm civil strife, stabilize the body's internal environment, and relieve all kinds of discomfort caused by inflammation.
    In summary, S-1,2,3,4-tetraamine-3-isopentenyl flavonoids are like a shining pearl in the field of medicine. With their diverse effects, they contribute to the cause of human health. In the future, it is expected to be further explored and developed to bloom more splendid and benefit all living beings.
    What are the synthesis methods of S-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid?
    There are various ways to synthesize S-1,2,3,4-tetraamine-3-isopentenyl flavonoid acid. The common ones can be obtained through the selection of starting materials and the design of reaction steps.
    First, an aromatic compound with a specific substituent is used as the starting material. First, it is reacted with an amine-containing reagent to construct an amine moiety. If an appropriate halogenated aromatic hydrocarbon is selected and reacted with a diamine compound such as ethylenediamine under alkali-catalyzed conditions in a suitable organic solvent, a preliminary amine-substituted product can be formed. This step requires attention to the reaction temperature and time. If the temperature is too high or the time is too long, or side reactions occur, the yield and purity will be affected. < Br >
    Then, the isopentenyl group is introduced. Allyl halide or isopentenol derivatives can be used to carry out the alkenylation reaction under the action of metal catalysts such as palladium catalysts. The control of this reaction condition is crucial, such as the amount of catalyst, ligand selection, etc., all of which have a significant impact on the selectivity and efficiency of the reaction. The structure and electronic properties of the ligand can change the activity and selectivity of the metal center, thereby leading to the formation of the target product.
    After subsequent steps such as oxidation or cyclization, the flavonoid acid structure is formed. If a specific intermediate product is oxidized with an appropriate oxidant, the carbonyl structure of flavonoid acid is constructed, and a cyclization reaction may be required to achieve the final structure of the target molecule. In this process, the polarity of the solvent, the pH of the reaction medium, etc. are all factors that need to be carefully regulated.
    Second, semi-synthesis can also be carried out from natural products. Some natural flavonoids, with similar parent nuclear structures, can be used as starting materials. By modifying their side chains, functional groups such as tetramine and isopentenyl are introduced. The advantage of this approach is that the inherent structure of natural products can be used to reduce reaction steps and improve reaction selectivity. However, the acquisition and purification of natural products may be difficult, and the stability and cost of the raw material source need to be considered.
    In short, the synthesis of S-1,2,3,4-tetraamine-3-isopentenyl flavonoid acid requires comprehensive consideration of starting materials, reaction conditions, catalyst and intermediate stability, and careful design of reaction routes to achieve high-efficiency and high-purity synthesis goals.
    What is the price range of S-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid in the market?
    I think this S-1,2,3,4-tetraamine-3-isopentenyl cinnamic acid product is difficult to determine in the market price range. Its price is often affected by various factors, making it difficult to generalize.
    First, the difficulty of obtaining raw materials and the cost have a great impact on its price. If raw materials are scarce, difficult to harvest, or difficult to prepare, the cost will increase, and the price will also be high.
    Second, the simplicity of the preparation process is also the key. If the preparation requires exquisite methods, complex steps, and strict requirements on equipment and the environment, the cost of manpower and material resources is huge, and the price will be high.
    Third, the trend of market supply and demand, especially the price. If there are many seekers, but there are few suppliers, the price will rise; if the supply exceeds the demand, the price may drop.
    Fourth, the difference in quality grade also makes the price different. High quality, few impurities, high purity, good performance, and the price should be higher than ordinary ones.
    Although it is difficult to determine its price range, it is speculated according to the market conditions of similar things. If the raw materials are common, the process is not complex, and the quality is ordinary, the price may be between tens and hundreds of currency units per unit; if the raw materials are rare, the process is complex, and the quality is excellent, the price may be thousands of currency units per unit, or even higher. This is all speculation, and the actual price should be subject to the real-time market conditions.