7 Methoxy 1 2 3 4 Tetrahydroisoquinoline Hcl
Quinoline Thiophene Imidazole Thiazole
7-METHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE HCL
Chemical Name 7-METHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE HCL
Molecular Formula C10H14ClNO
Molecular Weight 201.68
Appearance Typically a solid
Solubility Soluble in certain organic solvents
Melting Point Characteristic melting point
Odor May have a specific odor
Ph Can affect pH in solution
Stability Has certain stability under normal conditions
Purity Varies based on production quality
FAQ

What is the main use of 7-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

7-Amino-1,2,3,4-tetrahydroisoquinoline-8-carboxylic anhydride is especially important for its main use. This compound is a key intermediary in the field of medicinal chemistry.

In the process of creation of Guanfu Medicine, 7-amino-1,2,3,4-tetrahydroisoquinoline-8-carboxylic anhydride is often the starting material for the synthesis of various bioactive molecules. With its unique chemical structure, it can be coupled and cyclized with other compounds through various reaction pathways to construct complex structures with specific pharmacological functions.

First, in the research and development of drugs related to the nervous system, this anhydride is often relied on as the base. Many new drugs for neurotransmitter regulation and nerve cell protection have been explored. 7-amino-1,2,3,4-tetrahydroisoquinoline-8-carboxylic anhydride can be derived to precisely act on nerve receptors, which is expected to provide a new strategy for the treatment of epilepsy, Parkinson's disease and other neurological diseases.

Second, in the field of anti-tumor drugs, this anhydride has also emerged. By chemical modification, it can have the ability to target specific proteins or signaling pathways of tumor cells, thereby inhibiting the proliferation of tumor cells and inducing their apoptosis, adding a sharp edge to the problem of cancer.

Furthermore, in the field of organic synthesis chemistry, 7-amino-1,2,3,4-tetrahydroisoquinoline-8-carboxylic anhydride, with its lively reactivity, provides the possibility to construct novel organic skeletons. Chemists can design and synthesize organic molecules with unique structures according to their characteristics, enrich the reservoir of organic compounds, and lay the foundation for the development of materials science, catalytic chemistry and other related fields.

To sum up, 7-amino-1,2,3,4-tetrahydroisoquinoline-8-carboxylic anhydride plays an indispensable role in many fields such as medicine and organic synthesis, and has a wide range of uses and promising prospects.

What are the physical properties of 7-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

7-Methyl-1,2,3,4-tetrahydroisoquinoline-8-carboxylic anhydride is a kind of organic compound. Its physical properties have the following characteristics:

Looking at its appearance, it is often in a solid state, but its exact color state varies depending on the purity and crystallization conditions, or it is a white to light yellow powder or a crystalline solid. This is due to the characteristics of its molecular structure, and the intermolecular force makes it tend to form solid aggregates.

In terms of its melting point, it is within a certain temperature range, and the specific value varies slightly depending on the measurement method and conditions. This melting point characteristic is due to the forces of intermolecular interactions, including van der Waals forces, hydrogen bonds, etc. When the external temperature rises to a certain level, these forces are overcome, and the substance then changes from solid to liquid.

As for solubility, in organic solvents, such as common ethanol and dichloromethane, etc., it shows a certain solubility. This is because the molecular structure of the compound has both polar and non-polar parts, and can form van der Waals forces, dipole-dipole interactions, etc. with organic solvent molecules, so that it can be dispersed in organic solvent systems. However, the solubility in water is relatively limited, because the strong hydrogen bond network between water molecules is difficult to effectively match the intermolecular forces of the compound, making it insoluble in water. < Br >
Its density is also a specific value, reflecting the mass distribution of the molecule in a unit volume, which is closely related to the size and structure of the molecule. The characteristics of density are of important significance in practical operations such as separation and purification.

In addition, the stability of the compound is acceptable under conventional conditions, but when exposed to specific conditions such as high temperature and strong oxidants, the molecular structure may change. This stability is derived from the strength of its chemical bonds and the stability of its molecular configuration. Under certain conditions, chemical bonds may be broken or rearranged, which may change their chemical and physical properties.

What are the chemical properties of 7-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

7-Methyl-1,2,3,4-tetrahydroisoquinoline-8-carboxylic acid amides are organic compounds with unique chemical properties. They contain nitrogen heterocycles and carboxylamide groups, resulting in certain alkalinity and nucleophilicity of the compound.

From the structure, the nitrogen atom in the nitrogen heterocycle has lone pairs of electrons, which can provide electron pairs to react with protons or compounds with missing electron centers, showing alkalinity and nucleophilicity. Under appropriate conditions, it can react with acids to form salts, and can also undergo nucleophilic substitution reactions with electrophilic reagents such as halogenated hydrocarbons, introducing new substituents on the nitrogen atom. In the carboxylamide group, the carbonyl group has an electron-absorbing effect, which reduces the electron cloud density of amide nitrogen atoms and makes the basicity weaker than that of nitrogen heterocyclic atoms. However, this group can participate in a variety of reactions, such as reacting with nucleophiles under strong basic conditions, resulting in amide bond cleavage; it can also be converted into nitrile groups through dehydration reactions.

The chemical properties of this compound are affected by the substituent group. The methyl power supply effect can increase the electron cloud density of nitrogen heterocyclic, and enhance its alkalinity and nucleophilicity; while the electronic effects and spatial effects of other substituents can also affect the reactivity and selectivity.

In addition, the compound may have certain physical properties, such as melting point, boiling point, solubility, etc. These properties are related to intermolecular forces, which affect its dissolution and separation and purification in different solvents. In short, the chemical properties of 7-methyl-1,2,3,4-tetrahydroisoquinoline-8-carboxylic acid amide are determined by its structure, and different reaction conditions and substituents will lead to various chemical reactions.

What are the synthesis methods of 7-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride?

To prepare 7-amino-1,2,3,4-tetrahydroisoquinoline-8-carboxylic acid methyl ester, there are various methods.

First, it can be obtained from the corresponding nitrogen-containing heterocyclic precursor through multi-step reaction. First, use a specific starting material, under suitable reaction conditions, through nucleophilic substitution reaction, introduce the desired functional group. For example, take an aromatic hydrocarbon with a suitable substituent and react it with a nitrogen-containing reagent in an organic solvent under the catalysis of a base to form a nitrogen-containing intermediate. This intermediate is then cyclized to construct the skeleton of isoquinoline. At the time of cyclization, the reaction temperature, time and the ratio of the reactants need to be finely regulated to make the cyclization reaction proceed smoothly and obtain the target ring structure. Subsequently, the substituents on the ring are modified through selective oxidation, reduction or esterification reactions to achieve the purpose of introducing carboxyl groups at specific positions and methylating them, while ensuring that the amino groups are not affected.

Second, the strategy of biomimetic synthesis can be used. Simulate the metabolic pathway and reaction mechanism in vivo, and choose natural products or their analogs with simple and easy-to-obtain structures as starting materials. Use common enzyme-catalyzed reactions in vivo, or similar chemical catalysis processes, to gradually construct complex target molecular structures. For example, the synthetic precursor of a certain type of alkaloid is used as the starting material to simulate the process of synthesizing alkaloids in vivo, and the structure of 7-amino-1,2,3,4-tetrahydroisoquinoline-8-carboxylate is gradually constructed through a series of enzymatic reactions or chemical catalytic reactions. Although this strategy requires in-depth understanding of the biosynthetic mechanism, and the reaction conditions are relatively mild and highly selective, it is often very demanding on the reaction technology and conditions.

Third, the coupling reaction catalyzed by transition metals can also be used. First, intermediates containing different fragments are synthesized, such as fragments containing amino groups and fragments containing isoquinoline rings with suitable substituents. Subsequently, with the help of transition metal catalysts, such as palladium, nickel, etc., with the assistance of ligands, the two are coupled to form the basic framework of the target molecule. The framework is then modified and converted to introduce the required carboxyl methyl ester groups. This method has high reaction efficiency, but fine screening and optimization of transition metal catalysts and ligands are required to improve the selectivity and yield of the reaction.

What is the price range of 7-methoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride in the market?

I look at the world of goods, there are many categories, and the price is also impermanent, fluctuating with the supply and demand of the market and the change of time. As for 7-methyl-1,2,3,4-tetrahydroisoquinoline-8-formate hydrochloride, the market price range is difficult to determine at this time.

The price of goods and goods under the sky depends not only on the nature of the goods, but also on many reasons. First, the amount of production, if there are many producers, the supply will exceed the demand, the price will decline; if the production is thin and the demand is large, the price will rise. Second, if it is used widely and narrowly, if it is used in various industries, it needs to be prosperous and the price is high; if it is used sparsely, it needs to be small and the price is flat. The third is the urgency of the time, and the urgent need of the time, although the price is high; if it is normal, the price will not be high.

The market is diverse, the differences between the north and the south, the changes of ancient and modern times, all make the price different. Although I have the intention to ask for its exact price, the market is not permanent, the price is not fixed, and the range of its price cannot be determined. If you want to know its exact price, you must visit the city in person, inquire about the business office, observe its recent transactions, and measure its supply and demand status, so that you can get a more accurate price. Then it can be obtained in a moment, and it may change in an instant. The impermanence of building the market is beyond human strength.