1 2 3 4 Tetrahydroisoquinoline 3 Carboxylic Acid Hydrochloride
quinoline thiophene imidazole thiazole

1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride

Taiy Chemical

    Specifications

    HS Code

    432134

    Name 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride
    Chemical Formula C10H12ClNO2
    Molecular Weight 213.66
    Appearance Solid (usually powder or crystalline)
    Solubility Soluble in some polar solvents like water to a certain extent
    Melting Point Specific value depending on purity, typically in a defined temperature range
    Pka Characteristic value related to its acidic properties
    Hazard Class May have certain health and safety hazards depending on exposure levels

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    General Information
    Where to Buy 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride in China?
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    Frequently Asked Questions

    As a leading 1,2,3,4-Tetrahydroisoquinoline-3-carboxylic acid hydrochloride supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the chemical properties of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid hydrochloride?
    1% 2C2% 2C3% 2C4-tetrahydroisoquinoline-3-carboxybenzamide is an organic compound with the following chemical properties:
    1. ** Acidic-basic **: The molecule contains both a carboxyl group (-COOH) and an amide group (-CONH -). The carboxyl group can ionize hydrogen ions and is acidic. It can neutralize with bases, such as reacting with sodium hydroxide to form corresponding carboxylate salts and water. The basic alkalinity of amides is weak, and the ability to accept protons is reduced due to the participation of lone pairs of electrons on the nitrogen atom in the conjugate system. However, under strong acid conditions, the amide nitrogen atom can accept protons, reflecting a certain alkalinity.
    2. ** Nucleophilic Substitution Reaction **: The carboxyl carbon of the carboxyl group is electrophilic and vulnerable to attack by nucleophilic reagents. If an esterification reaction occurs with an alcohol catalyzed by an acid to form an ester and water, in this reaction, the alcohol hydroxyl oxygen atom attacks the carboxyl carbon as a nucleophilic reagent and forms an ester through a series of intermediates. In the amide group, the nitrogen atom of the amino group (-NH-) has a lone pair of electrons, which can participate in the reaction as a nucleophilic reagent. Like the reaction with halogenated hydrocarbons, the nitrogen atom attacks the carbon atom of the halogenated hydrocarbons, and the halogenated atom leaves to form a new carbon-nitrogen bond compound.
    3. ** Redox Reaction **: Unsaturated bonds Under the action of suitable oxidizing agents, unsaturated bonds may be oxidized to increase the oxygen atoms in the molecule or decrease the hydrogen atoms; under the action of reducing agents, unsaturated bonds can be reduced to increase the hydrogen atoms or decrease the oxygen atoms. For example, with strong reducing agents such as lithium aluminum hydride, the amide group can be reduced to an amine group, so that the structure and properties of the compound can be changed.
    4. ** Aromatic properties and π-π stacking **: The part of tetrahydroisoquinoline contains aromatic rings, which are aromatic and have high stability. It can undergo typical reactions of aromatic compounds, such as electrophilic substitution reactions. Pi-π stacking can occur due to the presence of aromatic rings between molecules, which affects the physical properties of the compound, such as melting point, solubility, etc. The chemical properties of this compound make it have potential applications in the fields of organic synthesis, medicinal chemistry, etc., and can be used as an intermediate to synthesize more complex compounds with specific biological activities.
    What are the main uses of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid hydrochloride?
    1% 2C2% 2C3% 2C4-tetrahydroisoquinoline-3-carboxylamide acid amide has a wide range of uses. In the field of medicine, it is often the key raw material for the creation of new drugs. Due to its unique chemical structure, it can interact with many biological targets in the human body, and then exhibit various pharmacological activities such as antibacterial, anti-inflammatory, and anti-tumor. For example, some targeted drugs for specific tumor cells may play an important role in the development of certain targeted drugs. By precisely acting on the specific molecular pathways of tumor cells, this compound can achieve the purpose of inhibiting tumor growth and spread.
    In the field of organic synthetic chemistry, it is an excellent intermediate for the construction of complex organic molecular structures. Chemists can use various organic reactions, such as nucleophilic substitution, addition reactions, etc., as a basis to ingeniously introduce different functional groups, expand the structural diversity of molecules, and synthesize organic compounds with unique properties and functions, providing novel compound entities for materials science, medicinal chemistry, and other fields.
    And it can be used as a biological probe in biochemical research. With its specific binding ability with biological macromolecules, it helps researchers gain insight into complex biochemical processes in organisms, such as protein-protein interactions, enzyme catalysis mechanisms, etc., providing a powerful tool for in-depth investigation of life sciences. In conclusion, 1% 2C2% 2C3% 2C4-tetrahydroisoquinoline-3-carboxylamide has important application value in the fields of medicine, organic synthesis and biochemical research, and promotes the continuous development of related disciplines.
    What are the synthesis methods of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid hydrochloride?
    1%2C2%2C3%2C4-%E5%9B%9B%E6%B0%A2%E5%BC%82%E5%96%B9%E5%95%89-3-%E7%BE%A7%E9%85%B8%E7%9B%90%E9%85%B8%E7%9B%90%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E6%9C%89%E5%A6%82%E4%B8%8B%E4%B8%83%E7%A7%8D%EF%BC%9A
    1. ** Using ethyl 4-bromobutyrate as the starting material **: Ethyl 4-bromobutyrate and diethyl malonate first undergo nucleophilic substitution under the action of sodium ethanol, and then alkaline hydrolysis, acidification and decarboxylation, the target product can be obtained. This process cleverly uses the nucleophilicity of diethyl malonate active methylene, and subsequent treatment to achieve specific structure construction.
    2. ** Using ethyl acrylate as the raw material **: ethyl acrylate is added with vinyl Grignard reagent, and the product can be obtained by hydrolysis and oxidation. With the strong nucleophilicity of Grignard reagent, carbon chain growth and structural transformation are achieved.
    3. ** Using succinic anhydride as raw material **: The succinic anhydride is first reacted with ethanol to obtain monoethyl succinate, and then condensed with formaldehyde under alkali catalysis. After dehydration, reduction and hydrolysis, the target product can be obtained. The ring-opening reaction of succinic anhydride and a series of subsequent transformations realize the synthesis of the product.
    4. ** Using crotonic acid as raw material **: The addition of crotonic acid to hydrogen bromide, the product is hydrolyzed, and then oxidized to obtain the target product. The addition of olefins to hydrogen halide and subsequent functional group conversion are used.
    5. ** Using ethyl acetoacetate as raw material **: Ethyl acetoacetate reacts with 1,3-dibromopropane, and the product is alkaline hydrolyzed, acidified and decarboxylated, and then oxidized The structure was constructed by the active methylene nucleophilicity of ethyl acetoacetate and subsequent reactions.
    6. ** Using 2-butenoic acid as raw material **: 2-butenoic acid reacts with N-bromosuccinimide (NBS) for bromination, and the product is hydrolyzed and oxidized to obtain the target product. Using the bromination selectivity of NBS and subsequent conversion.
    7. ** Using gamma-butyrolactone as raw material **:γ - butyrolactone to obtain 4-hydroxybutyric acid, 4-hydroxybutyric acid reacts with brominating agent to obtain 4-bromobutyric acid, 4-bromobutyric acid is then esterified with ethanol, and finally the target product can be obtained through a specific reaction. Synthesis is achieved by hydrolysis of lactone and subsequent functional group transformation.
    What is the market price of 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid hydrochloride?
    What is the market price of 1% 2C2% 2C3% 2C4-tetrahydroisoquinoline-3-carboxylamide amide today? This is a specific compound in the field of fine chemicals, and its price fluctuates due to many factors such as quality, purity, market supply and demand.
    In terms of quality and purity, those with high purity have complicated preparation processes, and the required raw materials and technical requirements are strict, so the price is high; those with low purity are relatively simple to prepare and relatively inexpensive. For example, those with a purity of 99% may sell for hundreds of yuan per gram; while those with a purity of only 90% may sell for only a few tens of yuan per gram.
    Market supply and demand conditions also affect its price. If the pharmaceutical and chemical industries have a large increase in demand for it at a certain time, but the supply is limited, the price will rise; if the demand is low and the supply is sufficient, the price will easily fall.
    In addition, factors such as manufacturers and sales regions also play a role. Different manufacturers have different cost and pricing strategies. They sell in economically developed and demand-strong regions, and their prices may be higher than other regions.
    For the exact market price, you can consult chemical raw material suppliers, relevant industry trading platforms, or refer to recent market transaction records, so that you can obtain relatively accurate price information.
    What are the precautions for storing and transporting 1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid hydrochloride?
    1% 2C2% 2C3% 2C4-tetrahydroisoquinoline-3-carboxylamide During storage and transportation, the following numbers should be paid attention to:
    First, it is related to the storage place. When placed in a warehouse, the warehouse must be kept cool and dry. It is easy to change the properties of this substance or cause it to deteriorate due to humidity and high temperature. It is necessary to avoid direct sunlight. Ultraviolet rays and other rays in the sun may affect its chemical structure and reduce its quality. The warehouse should also be well ventilated to prevent the local concentration from being too high due to lack of air circulation, which may cause potential risks.
    Second, discuss the packaging for storage. The packaging must be tightly sealed to prevent contact with oxygen, water vapor and other ingredients in the air. It is recommended to use suitable moisture-proof and anti-oxidation packaging materials, such as sealed plastic bags, glass bottles and sealed corks, etc., which can effectively prolong the shelf life of this item.
    Third, about the conditions of transportation. During transportation, it is necessary to avoid severe vibration and collision, because it may cause damage to the packaging, which may expose the item to the external environment. At the same time, the transportation tool should also maintain relatively stable temperature and humidity conditions. According to the characteristics of the item, consider using transportation equipment with temperature control and humidity adjustment functions to ensure the stability of the item during transportation.
    Fourth, personnel should also be cautious in operation. Whether it is handling, stacking during storage, or loading and unloading during transportation, relevant personnel should undergo professional training, be familiar with the characteristics and precautions of this object, and act in strict accordance with the operating procedures to avoid accidents caused by improper operation.
    In general, the storage and transportation of 1% 2C2% 2C3% 2C4 - tetrahydroisoquinoline - 3 - carboxylamide requires all-round consideration of the environment, packaging, operation and many other factors to ensure its quality and safety.