1 Chloro 4 Hydroxyisoquinoline
Quinoline Thiophene Imidazole Thiazole
1-Chloro-4-hydroxyisoquinoline
Name 1-Chloro-4-hydroxyisoquinoline
Chemical Formula C9H6ClNO
Molar Mass 179.60 g/mol
Appearance Solid (predicted, no common data on exact appearance in most cases)
Melting Point No common standard data available, needs experimental determination
Boiling Point No common standard data available, needs experimental determination
Solubility In Water Low solubility (due to its relatively non - polar aromatic structure and weak polar functional groups)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, etc. (due to its organic nature)
Pka No common standard data available, needs experimental determination
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
FAQ

What are the chemical properties of 1-Chloro-4-hydroxyisoquinoline?

1-Chloro-4-hydroxyisoquinoline is an organic compound with unique chemical properties. It contains chlorine atoms and hydroxyl groups, which have a great influence on the chemical behavior of the substance.

Let's talk about chlorine atoms first. They are electron-absorbing, which reduces the electron cloud density of benzene rings, making it more difficult for electrophilic substitution reactions to occur. However, under certain conditions, chlorine atoms can participate in nucleophilic substitution reactions. For example, when encountering strong nucleophiles, such as sodium alcohols or amines, chlorine atoms will be replaced by nucleophilic reagents to form new compounds. This is because the high electron cloud density of nucleophilic reagents has a strong attraction to partially positively charged chlorine atoms, which prompts the reaction to occur.

Looking at the hydroxyl group again, it has the property of electron conductors, which can increase the electron cloud density of the benzene ring, making the benzene ring more prone to electrophilic substitution. The electron cloud density of the adjacent and para-position hydroxyl groups increases particularly significantly, and electrophilic reagents tend to attack these positions. Moreover, the hydrogen atoms in the hydroxyl group have a certain acidity, and under alkaline conditions, it is easy to react with bases. The hydroxyl group exists in the form of oxygen negative ions, which is more nucleophilic and can participate in a variety of nucleophilic reactions.

The chlorine atom of 1-chloro-4-hydroxyisoquinoline and the hydroxyl group may also interact with each other. The electron-absorbing action of the chlorine atom also affects the hydroxy acidity and the substitution reaction activity on the benzene ring.

In addition, the structure of the isoquinoline ring in this compound also contributes significantly to its chemical properties. The isoquinoline ring is aromatic and relatively stable, but it can also undergo a variety of reactions based on aromatic rings, such as oxidation and reduction reactions. Under the action of appropriate oxidants, the isoquinoline ring may be oxidized, changing its structure and properties; under the action of reducing agents, a reduction reaction may occur, resulting in products with different saturation levels. In short, 1-chloro-4-hydroxyisoquinoline is rich in chemical properties due to its chlorine atom, hydroxyl group and isoquinoline ring structure, and has broad application potential in the field of organic synthesis.

What are the common synthetic methods of 1-Chloro-4-hydroxyisoquinoline?

For the synthesis of 1-chloro-4-hydroxyisoquinoline, the method is often based on isoquinoline and obtained through several steps.

First, the isoquinoline is exposed to the appropriate halogenating agent. If chlorine gas or chlorine-containing reagents are added, with the help of suitable temperature and catalytic agent, chlorine atoms can be introduced into the isoquinoline ring to obtain chloroisoquinoline. In this step, attention should be paid to the temperature control and the amount of agent to prevent the appearance of perhalogen.

Times, on the chloroisoquinoline, a hydroxyl group is introduced. The method of nucleophilic substitution is often used. A hydroxyl donor, such as an alkali metal hydroxide solution, is co-placed with chloroisoquinoline. After heating and other operations, the chlorine is replaced by the hydroxyl group to obtain 1-chloro-4-hydroxyisoquinoline. However, this step also needs to be carefully observed. Due to the different reaction conditions, or side reactions, the product is impure.

Or there are other methods, such as using a benzene ring with a specific substituent and a nitrogen-containing reagent, through cyclization, the framework of isoquinoline is formed first, and then halogenation and hydroxylation are carried out, which can also achieve the purpose of synthesis. However, these methods require careful selection of reagents and conditions to promote the reaction and increase the yield and purity of the product. When synthesizing, the method needs to be carefully selected according to the ease of access to raw materials, the level of cost, the difficulty of reaction and the purity of the product, etc., in order to achieve the best results.

In what areas is 1-Chloro-4-hydroxyisoquinoline applied?

1-Chloro-4-hydroxyisoquinoline is useful in various fields such as medicine and chemical industry.

In the field of medicine, this compound has attracted much attention. Due to its unique chemical structure, it has potential biological activity and can be used as a key intermediate in drug development. Or it can participate in the construction of molecules with specific pharmacological activities to explore new therapeutic drugs. For example, in the research of anti-tumor drugs, this compound can be modified and modified to target specific tumor cells, inhibit tumor growth and spread, and find a new way to overcome cancer problems. In the development of drugs for the treatment of nervous system diseases, or with its structural properties, drugs that regulate neurotransmitters and repair nerve damage can be developed.

In the chemical industry, 1-chloro-4-hydroxyisoquinoline also has important uses. It can be used as an important raw material for organic synthesis and participates in the preparation of a variety of fine chemicals. For example, in dye synthesis, it can endow dye molecules with special structures and properties, making dyes more colorful and better fastness. In the preparation of functional materials, materials synthesized based on this may have unique electrical and optical properties, and are used in electronic devices, optical instruments, etc., injecting vitality into the innovation and development of the chemical industry. Therefore, 1-chloro-4-hydroxyisoquinoline is widely used in medicine, chemical industry and other fields, and is of great significance to promoting technological progress and industrial development in related fields.

What are the physical properties of 1-Chloro-4-hydroxyisoquinoline?

1-Chloro-4-hydroxyisoquinoline is a kind of organic compound. Its physical properties are particularly important, and it is related to its performance in various chemical processes and practical applications.

First of all, its appearance is usually solid, but its specific color may vary depending on the purity and preparation method. Generally speaking, the purer ones are often white to light yellow powder, just like the thin snow that falls in the early winter, delicate and pure.

As for the melting point, this is the key indicator to identify and consider the thermal stability of the compound. The melting point of 1-chloro-4-hydroxyisoquinoline is within a certain range. At this temperature, it gradually melts from a solid state to a liquid state, just like ice and snow melting in the warm sun. The exact value of the melting point depends on accurate measurement, but it is roughly in a certain range. The range of this range provides an important reference for chemists in operation and reaction design.

In terms of solubility, its performance varies in organic solvents. In some organic solvents, such as dichloromethane, N, N-dimethylformamide, etc., it has a certain solubility. If it is soluble, it is like fine sand integrated into water, uniformly dispersed, and forms a uniform system. However, in water, its solubility is relatively poor, like a stubborn stone entering water, and it is difficult to blend with water. This difference in solubility needs to be carefully considered when separating, purifying and selecting the reaction medium.

Its density is also an important physical property. Although the specific value needs to be accurately determined, this density characteristic is indispensable in the measurement of materials in chemical production and the determination of mixing proportions. It is like a balance weight, accurately measuring its weight in various systems.

In addition, the vapor pressure of 1-chloro-4-hydroxyisoquinoline is low, and under room temperature and pressure, the degree of volatilization is limited, just like a quiet lake, which makes it relatively stable in general storage and operating environments, and it is not easy to be lost due to volatilization or cause safety risks.

In summary, the physical properties of 1-chloro-4-hydroxyisoquinoline, such as appearance, melting point, solubility, density and vapor pressure, are interrelated, and together they paint a unique "picture" in the chemical world, laying a solid foundation for its application in many fields such as organic synthesis and drug development.

What is the market price of 1-Chloro-4-hydroxyisoquinoline?

What you are asking is the market price of 1-chloro-4-hydroxyisoquinoline. However, it is difficult to determine the price of this chemical. The price of this chemical often changes due to various factors, and it is not static.

First, the price of raw materials has a great impact. If the price of raw materials required for the preparation of 1-chloro-4-hydroxyisoquinoline rises and falls suddenly, the price of the finished product will also fluctuate. If raw materials are scarce and supply exceeds demand, the price will rise; conversely, if raw materials are abundant and supply exceeds demand, the price may fall.

Second, the preparation method is related to cost. Different preparation processes require different human, material and financial resources. Sophisticated and efficient methods, although the upfront investment may be large, may reduce costs in the long run, which in turn affects the market price. And complicated and inefficient methods, high costs, and low prices.

Third, the state of market supply and demand determines the price. If many merchants need this chemical, and the demand exceeds the supply, the price will rise; if the demand is meager and the supply exceeds the demand, the merchant will sell its goods or reduce the price.

Fourth, regional differences also have an impact. In different places, prices may vary due to differences in transportation costs, tax policies, and market environments.

To sum up, in order to know the exact market price of 1-chloro-4-hydroxyisoquinoline, it is necessary to check the chemical product trading platform in real time, consult the industry merchants or relevant experts, in order to obtain the current accurate price.