N 1 3 Benzodioxol 5 Ylmethyl 3 Chloro 1 Benzothiophene 2 Carboxamide
Quinoline Thiophene Imidazole Thiazole
N-(1,3-benzodioxol-5-ylmethyl)-3-chloro-1-benzothiophene-2-carboxamide
Chemical Formula C17H12ClNO3S
Molecular Weight 345.80
Appearance Solid (predicted)
Solubility Solubility in water is low (predicted), may dissolve in organic solvents like DMSO
Logp Predicted to have significant lipophilicity
Vapor Pressure Very low (predicted for a solid)
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
FAQ

What is the chemical structure of N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-1-benzothiophene-2-formamide?

This is a structural problem of organic compounds. N- (1,3-naphthaleno-dioxacyclopentene-5-ylmethyl) -3-chloro-1-naphthaleno-pyrrole-2-acetamide, the structure of this compound is quite complex and consists of several parts.

1,3-naphthaleno-dioxacyclopentene, this is a cyclic structure, the naphthalene ring is merged with dioxacyclopentene, and there is a methyl group attached at the 5th position. This part constitutes one end of the compound. And 3-chloro-1-naphthalene-pyrrole-2-acetamide, in which naphthalene-pyrrole is a fused ring structure, the pyrrole ring is connected to the naphthalene ring, and there is a chlorine atom substitution at position 3, and the acetamide group at position 2 is connected. This part is another key part of the compound.

Acetamide is formed by connecting acetyl and amino groups, and is connected to naphthalene-pyrrole at position 2. The structure of this compound is closely connected, and a specific spatial structure is constructed by chemical bonds. Such a complex structure endows the compound with unique chemical properties and potential biological activities, which may be of important research value in the fields of organic synthesis and medicinal chemistry.

What are the physical properties of N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-1-benzothiophene-2-formamide

N- (1,3-benzodioxacyclopentene-5-methyl) -3-chloro-1-benzofuran-2-acetamide is an organic compound with unique physical properties. Its appearance is usually white to light yellow crystalline powder, which is stable in solid state and has certain tolerance to light and heat. However, it may be at risk of decomposition under high temperature or long-term light.

The melting point of this compound is about [specific melting point value] ℃. This melting point characteristic is of great significance for its separation and identification during synthesis and purification. Its purity can be determined by melting point. In terms of boiling point, at a specific pressure, it is about [specific boiling point value] ° C. This boiling point data is quite critical in separation operations such as distillation.

In terms of solubility, N- (1,3-benzodioxane-5-methyl) - 3-chloro-1-benzofuran-2-acetamide is insoluble in water, because it has a large proportion of hydrophobic groups in the molecule and has a weak force with water molecules. However, it is soluble in common organic solvents, such as dichloromethane, chloroform, acetone, etc., and has good solubility in these solvents. Taking advantage of this difference in solubility, in organic synthesis and separation, suitable solvents can be selected to dissolve, extract, recrystallize and other operations to achieve separation and purification.

The density is about [specific density value] g/cm ³. This density data can guide the determination of its dosage and volume during the development and production of formulations. In addition, the chemical properties of the compound are relatively stable at room temperature and pressure, but in the presence of strong acids, strong bases or strong oxidants, some chemical bonds in its molecular structure may react, such as amide bonds under strong acids or strong bases or hydrolysis, which affects its chemical stability.

What is the main use of N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-1-benzothiophene-2-formamide?

N- (1,3-benzodioxacyclopentene-5-ylmethyl) -3-chloro-1-benzofuran-2-acetamide has a wide range of uses. In the field of medicine, it can be used as an important pharmaceutical intermediate, laying the foundation for the synthesis of many drugs. For example, in the preparation of some compounds with specific physiological activities, it acts as a key starting material. After a series of delicate chemical reactions, it can construct complex structural drugs with specific pharmacological effects, thus providing effective means for the treatment of diseases.

In the chemical industry, it also plays an important role. It can be used to prepare polymer materials with special properties. With the help of polymerization with other monomers, polymer materials are endowed with unique physical and chemical properties, such as improving the stability of materials and improving their solubility, which in turn meets the diverse needs of different industrial scenarios for material properties.

In addition, in organic synthesis research, it is a commonly used synthetic building block that can help chemists design and construct novel organic compounds, providing new ideas and methods for the development of organic synthesis chemistry, promoting the field to continue to expand and explore more unknown chemical space to meet the growing demand for new organic compounds in science and technology and industrial development.

What are the synthesis methods of N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-1-benzothiophene-2-formamide

To prepare N- (1,3-naphthaleno-dioxacyclopentene-5-ylmethyl) -3-fluoro-1-naphthaleno-pyrrole-2-acetamide, the method is as follows:
First, a multi-step reaction can be performed to construct the structural units of naphthaleno-dioxacyclopentene and naphthaleno-pyrrole. For the 1,3-naphthaleno-dioxacyclopentene part, a suitable naphthalol derivative can be selected, and the naphthaleno-dioxacyclopentene structure is formed by nucleophilic substitution reaction with dihalogenated alkanes under basic conditions, and then 5-ylmethyl is introduced.
For 3-fluoro-1-naphthalene-pyrrole-2-acetamide fragments, fluorine atoms can be introduced by halogenation from naphthalene, and then pyrrole rings can be constructed through a series of reactions, followed by reaction with acetyl-related reagents to introduce acetyl groups, and then react with suitable amines to form amides.
Then, the above-constructed two-part structure is combined under suitable reaction conditions through a suitable linking reaction, such as amidation in the presence of a condensing agent, so that the two are connected to obtain the target product N- (1,3-naphthaleno-dioxane-5-ylmethyl) -3-fluoro-1-naphthaleno-pyrrole-2-acetamide. This synthetic route requires attention to the precise control of the reaction conditions at each step to ensure the smooth progress of the reaction and the purity and yield of the product.

What is the market outlook for N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-1-benzothiophene-2-formamide?

Now there is a market prospect of N- (1,3-benzo heterocyclopentene dioxide-5-ylmethyl) -3-chloro-1-benzofuran-2-acetic acid.

This compound has great potential in the field of pharmaceutical chemistry. The structure of benzofuran and benzo heterocyclopentene dioxide gives it unique physical and chemical properties, or it can exhibit specific biological activities. In the process of drug development, it can be used as a key intermediate to construct molecules with specific pharmacological effects.

Looking at the pharmaceutical market today, there is an increasing demand for innovative drugs. Many difficult diseases such as cancer and neurodegenerative diseases urgently require novel treatment methods. If this compound is confirmed to have significant biological activity, it may become an important cornerstone for the development of related drugs. It may be able to develop drugs with high efficiency and low toxicity for specific targets, and the market prospect is quite promising.

In the field of materials science, compounds containing such structures may exhibit special optoelectronic properties. With the development of miniaturization and high performance of electronic devices, the demand for new optoelectronic materials is increasing. If this compound is modified and optimized to exhibit excellent photoelectric properties, such as high fluorescence quantum yield, good charge transfer ability, etc., it will find applications in organic Light Emitting Diode (OLED), solar cells, etc., and its market demand will also rise.

However, its market prospects are also constrained by many factors. The complexity and cost of the synthesis process have a great impact on its large-scale production and marketing activities. If the synthesis route is long, the conditions are harsh, the yield is low, and the cost remains high, it will be difficult to gain an advantage in the market competition. Furthermore, regulatory supervision and safety assessment are also key. In the field of medicine, new drugs must undergo rigorous clinical trials and approval to ensure safety and effectiveness before they can be marketed; in the field of materials, they must also meet relevant environmental protection and safety standards.

In summary, if N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-1-benzofuran-2-acetic acid can overcome the problems of synthesis and regulations, it may open up a vast world in the pharmaceutical and materials market, and the prospect is promising.