2 3 Oxobenzo B Thien 2 3h Ylidene Benzo B Thiophene 3 2h One
quinoline thiophene imidazole thiazole

2-(3-oxobenzo[b]thien-2(3H)-ylidene)benzo[b]thiophene-3(2H)-one

Taiy Chemical

Specifications

HS Code

664444

Chemical Formula C18H8O2S2
Molecular Weight 332.4
Appearance Solid (predicted from structure)
Solubility In Water Low (due to non - polar nature of the aromatic rings)
Solubility In Organic Solvents Soluble in non - polar organic solvents like dichloromethane, toluene (predicted from structure)
Stability Stable under normal conditions (but may be sensitive to strong oxidizing agents)
Uv Vis Absorption Absorption bands in the visible and UV regions due to conjugated π - systems
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General Information
Frequently Asked Questions
What is the chemical structure of 2- (3-oxobenzo [b] thien-2 (3H) -ylidene) benzo [b] thiophene-3 (2H) -one
This is the name of an organic compound. To derive its chemical structure according to this name, it is necessary to analyze the meaning of each part. "2 - (3 - oxybenzo [b] thiophene - 2 (3H) -subunit) benzo [b] thiophene - 3 (2H) -ketone", where "benzo [b] thiophene" indicates that the structure contains a parent nucleus formed by fusing the benzene ring with the thiophene ring, and the sulfur atom is at a specific position (b position). "2 (3H) -subunit" and "3 (2H) -ketone" refer to the double bond and carbonyl at a specific location, respectively. " 2 - (3 -oxybenzo [b] thiophene-2 (3H) -subunit) "means that the second position of benzo [b] thiophene-3 (2H) -ketone is connected to a substituent composed of 3-oxybenzo [b] thiophene-2 (3H) -subunit. Among this substituent, the 3-oxygen representative has a carbonyl group at the third position of benzo [b] thiophene.
In summary, its chemical structure is: benzo [b] thiophene-3 (2H) -ketone is used as the parent nucleus, and a 3-oxybenzo [b] thiophene-2 (3H) -subunit is connected at 2 positions. The benzo [b] thiophene ring of the parent nucleus is fused with the thiophene ring, the 3 position is carbonyl, and the 2 position is connected with a substituent. The benzo [b] thiophene of the substituent is also fused with the thiophene ring by the benzene ring, with a carbonyl group at 3 positions, and the 2 positions are connected to the parent nucleus in the form of subunits. This structure is complex, contains multiple ring structures and functional groups at specific positions, and is used in the field of organic chemistry or has specific chemical properties and reactivity.
What are the physical properties of 2- (3-oxobenzo [b] thien-2 (3H) -ylidene) benzo [b] thiophene-3 (2H) -one
2-%283-oxobenzo%5Bb%5Dthien-2%283H%29-ylidene%29benzo%5Bb%5Dthiophene-3%282H%29-one is an organic compound. Its physical properties are very important, and it is related to its application in various fields.
When it comes to appearance, this compound often takes a specific form, either crystalline or powdered, depending on the preparation conditions and the structure of the molecule itself. The morphology of crystallization is related to the lattice arrangement, and the particle size of the powder also affects its appearance.
Melting point is one of the key physical properties. The melting point of the compound reflects the strength of intermolecular forces. Intermolecular forces include van der Waals forces, hydrogen bonds, etc. The interaction of atoms in the molecular structure of this compound determines the melting point. If the intermolecular forces are strong, a higher energy is required to disintegrate the lattice, and the melting point is high; otherwise, it is low. The boiling point of
cannot be ignored either. The boiling point is related to molecular volatility, and the boiling point of this compound determines the difficulty of changing from liquid to gaseous state at a specific temperature and pressure. The boiling point is affected by factors such as molecular weight, intermolecular forces, and molecular shape.
In terms of solubility, it shows different behaviors in different solvents. This is related to the interaction between solvents and solute molecules, and follows the principle of "similar miscibility". If the compound is a polar molecule, its solubility may be better in polar solvents; non-polar compounds are more soluble in non-polar solvents. Understanding its solubility is of great significance for the study of its separation, purification, and reaction in solution systems.
Density is also one of the physical properties, reflecting the mass of matter per unit volume. The density of the compound depends on its molecular weight and the way it is deposited. In the field of material applications, density affects the properties and uses of the material.
In addition, the compound may have specific optical properties, such as absorption and emission of light of specific wavelengths. This is due to the structural characteristics such as electron transitions and conjugate systems in the molecular structure that affect its optical behavior, and may have potential applications in the fields of optical materials and other fields.
What is the synthesis method of 2- (3-oxobenzo [b] thien-2 (3H) -ylidene) benzo [b] thiophene-3 (2H) -one
There are currently 2 - (3 - oxybenzo [b] thiophene - 2 (3H) -subunit) benzo [b] thiophene - 3 (2H) -one synthesis, the method is as follows:
First, the corresponding starting materials need to be prepared. The synthesis of this compound is often based on compounds containing benzothiophene structures. Select suitable 2 - methylbenzo [b] thiophene derivatives, which can be modified by specific reactions due to their methyl activity. Next, the methylation of 2-methylbenzo [b] thiophene derivatives is oxidized to carbonyl by chemical oxidation. Strong oxidants such as chromic acid can be used to precisely control the reaction process under suitable reaction conditions to obtain 3-oxybenzo [b] thiophene-2 (3H) -one intermediates. In this step, attention should be paid to the reaction temperature, time and oxidant dosage to prevent the product from being impure due to excessive oxidation.
Furthermore, the obtained 3-oxybenzo [b] thiophene-2 (3H) -one intermediate is taken and condensed with another benzo [b] thiophene derivative. Usually a base is used as a catalyst, such as an organic base such as piperidine, in an organic solvent, heating prompts the condensation of the two to form the target product 2- (3-oxybenzo [b] thiophene-2 (3H) -subunit) benzo [b] thiophene-3 (2H) -one. This step requires controlling the pH of the reaction system, temperature and the proportion of reactants to improve the reaction yield.
After the reaction is completed, a pure target product can be obtained by suitable separation and purification methods, such as column chromatography. Through these steps, 2 - (3 -oxybenzo [b] thiophene-2 (3H) -subunit) benzo [b] thiophene-3 (2H) -one can be obtained. During the synthesis process, the precise control of the reaction conditions of each step is the key to obtain high purity and high yield products.
What are the application fields of 2- (3-oxobenzo [b] thien-2 (3H) -ylidene) benzo [b] thiophene-3 (2H) -one
2-%283-oxobenzo%5Bb%5Dthien-2%283H%29-ylidene%29benzo%5Bb%5Dthiophene-3%282H%29-one is an organic compound with unique structure and properties, which can be used in many fields.
In the field of materials science, this compound can be used as an organic semiconductor material. Because of its structure, it can move electrons, so it has attracted much attention in the fabrication of organic field effect transistors, organic Light Emitting Diodes and other devices. By adjusting its chemical structure, it can improve the electrical and optical properties of materials, improve device performance, such as enhancing the luminous efficiency and stability of organic Light Emitting Diodes, expand its application in display technology, and make the display picture clearer and brighter.
In the field of optics, the compound may have special photophysical properties, such as fluorescence properties. It can be used in the design of fluorescent probes to generate fluorescence signal changes in response to specific substances or environmental changes, and to realize the detection and imaging of biomolecules, ions, etc. In biomedical research, biomolecules can be tagged to help observe biological processes and molecular interactions in organisms, providing important information for disease diagnosis and treatment.
In the field of organic synthesis, it is used as a key intermediate for the synthesis of more complex organic compounds. Organic chemists can use its special structure to carry out various chemical reactions, build new carbon-carbon bonds or carbon-heteroatomic bonds, and synthesize organic molecules with specific functions, providing an effective way for the development of new drugs and the total synthesis of natural products. For example, in the development of new drugs, a series of structural analogs are synthesized using it as a starting material, and lead compounds with potential medicinal value are screened for by activity.
What is the market outlook for 2- (3-oxobenzo [b] thien-2 (3H) -ylidene) benzo [b] thiophene-3 (2H) -one?
2-%283-oxobenzo%5Bb%5Dthien-2%283H%29-ylidene%29benzo%5Bb%5Dthiophene-3%282H%29-one, this is the name of an organic compound, and its market prospect is related to many factors. Looking at today's chemical materials and scientific research fields, let me come one by one.
Looking at this compound, its structure is unique, and it may have special optical and electrical properties in material science. In the field of optoelectronic materials, there is a growing demand for high-efficiency luminescent and conductive materials. If this compound is proved to have excellent photoelectric conversion efficiency or unique luminescent properties, it will attract the attention of the scientific research community and industry. If OLED display technology continues to develop, there is an urgent demand for new luminescent materials. If this compound is suitable for OLED, its market prospect will be extremely broad, or it will become the object of many display technology companies competing for research and development and application.
Furthermore, in the field of organic synthesis chemistry, this compound may be an important intermediate. Organic synthesis aims to construct various complex organic molecules for drug research and development, material preparation, etc. If it can be easily converted into other high-value compounds, chemical synthesis companies may have a large demand for it as raw materials for key synthesis links in order to develop new synthesis routes and products.
However, its market prospects also pose challenges. First, it may be difficult to synthesize this compound. If the preparation process is complicated and costly, even if the performance is excellent, commercialization will be hindered. Because companies pursue cost-effectiveness, it is difficult to have market competitiveness if the cost is too high. Secondly, it is necessary to study its stability, toxicity and other properties in depth. In practical applications, the material stability is not good, and it is difficult to be widely used; if the toxicity does not meet the relevant standards, the application in medicine, consumer electronics and other fields is limited.
In general, if 2-%283-oxobenzo%5Bb%5Dthien-2%283H%29-ylidene%29benzo%5Bb%5Dthiophene-3%282H%29-one can overcome the problems of synthesis and property research, with its unique structure and potential properties, it may open up a vast market in the fields of optoelectronic materials and organic synthesis; on the contrary, if it is difficult to solve the existing problems, the market road may be full of thorns, and it is difficult to make a big difference.