S 6 7 Dimethoxy 1 2 3 4 Tetrahydro 3 Isoquinolinecarboxylic Acid Hydrochloride
Quinoline Thiophene Imidazole Thiazole
(S)-6,7-Dimethoxy-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid hydrochloride
Chemical Name (S)-6,7-Dimethoxy-1,2,3,4-tetrahydro-3-isoquinolinecarboxylic acid hydrochloride
Molecular Formula C12H16ClNO4
Molecular Weight 273.71
Appearance Solid (predicted)
Melting Point No data available
Boiling Point No data available
Solubility Soluble in water (predicted)
Pka No data available
Logp No data available
Chirality S - enantiomer
Cas Number No data available
FAQ

What is the chemical structure of (S) -6,7-dimethoxy-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid hydrochloride

(S) -6,7-diethoxy-1,2,3,4-tetrahydro-3-isopropylbenzoic anhydride, its chemical structure is also quite complex.

Looking at this structure, its core is the structure of benzoic anhydride. The benzoic anhydride is an acid anhydride compound formed by the dehydration and condensation of benzoic acid. In this compound, diethoxy is introduced at positions 6 and 7. The ethoxy group is formed by connecting the ethyl group to the oxygen atom. It is the power supply group, which can affect the electron cloud density and chemical activity of the molecule.

Furthermore, the structure of 1,2,3,4-tetrahydro shows that the partial hydrogenation of the benzene ring changes the original benzene ring conjugate system, which in turn affects the stability and reaction characteristics of the compound. The existence of 3-isopropylene group adds an unsaturated carbon-carbon double bond structure to the molecule. The double bond activity of isopropylene group is high, and many reactions such as addition and polymerization can occur, which greatly enriches the chemical properties of this compound.

(S) indicates that the compound has chirality and exists a specific spatial configuration. The existence of chirality makes the compound exhibit unique properties in terms of biological activity and optical activity. The chemical behavior and physical properties of (S) -6,7-diethoxy-1,2,3,4-tetrahydro-3-isopropylbenzoic anhydride are determined by the interaction of various parts in this structure, which may have important significance and potential application value in the fields of organic synthesis and medicinal chemistry.

What are the physical properties of (S) -6,7-dimethoxy-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid hydrochloride

(S) -6,7-diethoxy-1,2,3,4-tetrahydro-3-isopropylbenzofuran-2-carboxylic acid, which is an organic compound. Its physical properties are crucial for its application in many fields.

Looking at its properties, it is likely to be white to light yellow crystalline powder at room temperature and pressure. This form is easy to store and transport, and it is also easier to handle when used in subsequent processing.

When talking about the melting point, it is about [X] ℃. The characteristics of the melting point can be used to identify the purity of the compound. If there are many impurities, the melting point will often be reduced and the melting range will become wider.

Its solubility also has characteristics, slightly soluble in water, but soluble in organic solvents such as ethanol, acetone, and dichloromethane. This solubility makes it possible to select suitable solvents according to the needs of the reaction during the chemical reaction to ensure the smooth progress of the reaction. In organic synthesis, the appropriate choice of organic solvents has a significant impact on the reaction rate and yield.

In addition, the density of the compound is about [X] g/cm ³. As one of the physical properties, density has reference value in the process of material measurement, mixing and other operations, which helps to accurately control the amount of reaction materials and achieve the desired reaction effect.

The physical properties of this compound have laid an important foundation for its research and application in chemical, pharmaceutical and other fields.

What are the common uses of (S) -6,7-dimethoxy-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid hydrochloride?

(S) -6,7-diethoxy-1,2,3,4-tetrahydro-3-isopentenyl benzoic anhydride, its common use is also quite specific. This compound is often a key intermediate in the field of organic synthesis.

The wonders of organic synthesis are just like ancient craftsmen carving utensils, which need to start with exquisite raw materials. (S) -6,7-diethoxy-1,2,3,4-tetrahydro-3-isopentenyl benzoic anhydride, often used as the cornerstone of building complex organic molecules. In the field of medicinal chemistry, it can undergo a series of subtle transformations to participate in the creation of drug molecules with specific biological activities, which is like a brick for doctors to find a good remedy for the world.

Furthermore, in the context of materials science, it may be integrated into the structure of polymer materials through specific reactions, giving materials unique properties, such as improving the stability and flexibility of materials, like injecting essence into materials, making them stand out in specific application scenarios.

And in the field of total synthesis of natural products, (S) -6,7-diethoxy-1,2,3,4-tetrahydro-3-isopentenylbenzoic anhydride also plays an important role. Synthetic chemists can skillfully design reaction routes according to their structural characteristics to achieve precise synthesis of complex natural products, just like recreating the wonders of nature. In short, this compound has its indispensable uses in many scientific fields, just like stars in the sky, although it is small but shining, illuminating the direction of scientific research.

What are the synthesis methods of (S) -6,7-dimethoxy-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid hydrochloride

To prepare (2S) -6,7-diethoxy-1,2,3,4-tetrahydro-3-isopropylbenzofuranone, the method is as follows:
First take an appropriate amount of starting materials, according to the ancient recipe, when operating in a fine way. A key reactant can be first placed in a specific reaction environment to initiate the reaction under mild conditions. In this reaction environment, the temperature needs to be precisely controlled, and the solvent used should be selected to be compatible with the reactant to make the reaction smooth.
After the initial product of the reaction in the first step, it needs to be separated and purified by a careful method. This purification method, either by extraction or distillation, depends on the characteristics of the product.
Then, the purified product is introduced into the second step of the reaction. In this step, a specific catalyst may be added to promote the rate and selectivity of the reaction. The amount of catalyst also needs to be carefully weighed, and more may cause side reactions, and less may cause slow reaction.
During the reaction process, when closely monitoring the reaction status. Or observe the change of its color, or measure its temperature, or use instruments to analyze its composition. In case of abnormalities, the reaction conditions need to be adjusted in time.
After the reaction is completed, the product is separated and purified again to obtain pure (2S) -6,7-diethoxy-1,2,3,4-tetrahydro-3-isopropylbenzofuranone. The whole process requires rigorous operation and attention to detail in order to achieve optimum yield and purity and produce the desired product.

What are the relevant safety precautions for (S) -6,7-dimethoxy-1,2,3,4-tetrahydro-3-isoquinoline carboxylic acid hydrochloride?

(S) -6,7-diethoxy-1,2,3,4-tetrahydro-3-isopropylbenzoic anhydride related safety precautions are as follows:

This substance is a chemical agent, which is related to the safety of experiments and production, and must not be taken lightly. First, in terms of storage, it should be placed in a cool, dry and well-ventilated place. Because of its chemical activity, high temperature and humid environment can easily deteriorate or cause dangerous reactions. For example, if the ambient humidity is too high, moisture may react with the substance such as hydrolysis, change its chemical properties, and even produce harmful gases.

Second, the operation process must be cautious. Appropriate protective equipment must be worn, such as protective gloves, goggles and protective clothing. The substance may be irritating to the skin and eyes, and inadvertent contact may cause skin burns, eye tingling and even vision damage. If you do not wear goggles during operation, once the substance splashes into the eyes, it will cause serious damage to the eye tissue.

Third, when taking and using, follow specific operating procedures. Avoid operating in open flames and hot topic environments, because they may be flammable, in case of open flames, hot topics, there is a risk of fire or even explosion. The operating site should be equipped with complete fire protection facilities for emergencies.

Fourth, waste disposal cannot be ignored. It cannot be discarded at will, and must be properly disposed of in accordance with relevant environmental protection regulations. Due to its special chemical properties, it can discard or pollute soil and water sources at will, endangering the ecological environment. Waste should be collected in a specific container and handed over to a professional organization for disposal.

Fifth, the relevant operators must be familiar with the nature, hazards and emergency treatment methods of the substance. In the event of an accident, such as leakage, contact with the human body, etc., it can be dealt with quickly and correctly. If the skin comes into contact, it should be rinsed with a lot of water immediately; if eaten by mistake, it is necessary to seek medical attention immediately and inform the doctor of the details of the exposed substance. In this way, the safety of personnel and the environment will not be damaged.