What is the chemical structure of N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-6-methoxy-1-benzothiophene-2-formamide?

This substance is called N- (1,3-naphthaleno-dioxacyclopentene-5-ylmethyl) -3-chloro-6-methoxy-1-naphthaleno-pyrrole-2-formamide, and its chemical structure is quite complex.

The main structure of this compound is composed of naphthaleno-pyrrole ring, naphthaleno-dioxacyclopentene and formamide group. Among them, 1-naphthalene-pyrrole-2-formamide is used as the core structure, the 2-position of the pyrrole ring is connected to the formamide group, and the nitrogen atom on the formamide group is connected to the 1,3-naphthalene-dioxacyclopentene-5-yl methyl group. In the 1,3-naphthalene-dioxacyclopentene structure, the 1,3-position is that two oxygen atoms merge with the naphthalene ring to form the dioxacyclopentene, and the 5-position is connected to the methyl group. The 3-position of the naphthalene-pyrrole ring is connected to the chlorine

The structures of naphthalene pyrrole ring and naphthalene dioxane in this structure endow the compound with unique physical and chemical properties. The existence of different substituents affects its reactivity, solubility and biological activity. It may have important applications in organic synthesis, pharmaceutical chemistry and other fields. It can be used as a lead compound for structural modification and optimization to develop drugs or materials with specific functions.

What are the main uses of N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-6-methoxy-1-benzothiophene-2-formamide?

N- (1,3-naphthalenedioxycyclopentene-5-methylphenyl) - 3-chloro-6-methoxy-1-naphthalene-pyrrole-2-formamide This substance has a wide range of uses.

In the field of medicine, it can be used as a key intermediate for the synthesis of drugs with specific biological activities. Due to its unique chemical structure, it can precisely bind to specific targets in organisms and exhibit potential pharmacological activity. Or can participate in the research and development of anti-tumor drugs, through the regulation of tumor cell proliferation and apoptosis-related signaling pathways, to inhibit tumor growth; in the development of drugs for nervous system diseases, it is also expected to play a therapeutic role by regulating neurotransmitter transmission, protecting nerve cells and other mechanisms.

In the field of materials science, it has unique optoelectronic properties, or can be used to prepare organic optoelectronic materials. For example, in the field of organic Light Emitting Diode (OLED), it can be used as a light-emitting layer material. Due to its structural characteristics, it can efficiently generate fluorescence when electrically excited, which is expected to improve the luminous efficiency and color purity of OLED; in the field of organic solar cells, it may also improve the photoelectric conversion efficiency of batteries by virtue of its good light absorption and charge transport capabilities. In the field of pesticide research and development, with its impact on certain biological activities, it can be developed as a new type of pesticide. It can specifically inhibit specific physiological processes of pests, such as interfering with insect growth and development, inhibiting the metabolism of pathogens, etc., thus effectively controlling crop diseases and insect pests, and is environmentally friendly, which is conducive to sustainable agricultural development.

What are the synthesis methods of N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-6-methoxy-1-benzothiophene-2-formamide?

To prepare N- (1,3-naphthaleno-dioxacyclopentene-5-methoxymethyl) -3-chloro-6-methoxy-1-naphthaleno-pyrrole-2-formamide, the following common organic synthesis paths can be started.

First, 1,3-naphthaleno-dioxacyclopentene-5-formaldehyde is used as the starting material. First, it is mixed with methanol and a suitable catalyst, and the acetalization reaction is carried out at a suitable temperature and pressure to obtain 1,3-naphthaleno-dioxacyclopentene-5-methoxymethyl acetal. Subsequently, it is halogenated with a specific halogenating agent in a suitable solvent, and chlorine atoms are introduced at a suitable check point. After that, the key carbon-carbon bonds are formed with the compounds containing the pyrrole structure under alkali catalysis and heating conditions, and the nucleophilic substitution reaction is carried out to form the pyrrole ring part. Finally, through the amidation reaction, the amide bond in the target product is formed with a suitable amine to obtain N- (1,3-naphthaleno-dioxy-cyclopentene-5-methoxy methyl) -3-chloro-6-methoxy-1-naphthaleno-pyrrole-2-formamide.

Second, starting from 3-chloro-6-methoxy-1-naphthalene-pyrrole-2-carboxylic acid. First, it is converted into the corresponding acid chloride, which can be reacted with oxalyl chloride or dichlorosulfoxide in the presence of catalyst. At the same time, 1,3-naphthalene-dioxane-5-methoxy methyl halide is prepared by reacting with halomethane under basic conditions with 1,3-naphthalene-dioxane-5-methoxy methyl halide. Next, the acid chloride is reacted with 1,3-naphthalene-dioxane-5-methoxy methyl halide under the catalysis of a suitable base to form the target product. This process requires strict control of the reaction conditions to prevent side reactions from occurring, such as the elimination of halogen atoms and cyclization.

Third, naphthalene phenols are used as the starting materials. The structure of naphthalene-dioxane is constructed by multi-step reaction, such as methoxylation and cyclization, and then the target product is prepared by a series of reactions such as halogenation, pyrrole ring construction and amidation. Although there are many steps in this path, the source of raw materials is extensive. In the synthesis, it is necessary to carefully optimize the reaction conditions at each step, control the reaction temperature, time, ratio of reactants and catalyst dosage, etc., in order to improve the reaction yield and selectivity, and obtain high purity N- (1,3-naphthaleno-dioxy-cyclopentene-5-methoxymethyl) -3-chloro-6-methoxy-1-naphthaleno-pyrrole-2-formamide.

What are the safety and toxicity of N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-6-methoxy-1-benzothiophene-2-formamide?

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This organic compound has a complex structure, and in order to investigate its essence, it needs to be analyzed in detail.

The "N- (1,3-naphthaleno heterocyclopentene dioxide-5-methylphenyl) -3-chloro-6-methoxy-1-naphthaleno-pyrrole-2-formamide" is said to have a unique molecular structure.

In terms of its safety, the safety of organic compounds is related to many ends. First, from the perspective of structure, naphthalenes contain naphthalene ring structure, and naphthalenes are mostly toxic. The existence of naphthaleno structure in this compound may suggest its potential toxicity risk. Second, the introduction of halogen atoms, that is, 3-chloro, halogenated hydrocarbons under certain conditions, or chemical reactions occur, generating harmful by-products, which affects their safety. Third, substituents such as methoxy and methylphenyl, although affecting the physical and chemical properties of molecules to a certain extent, may also participate in the reaction under specific circumstances and change the activity and toxicity of compounds.

As for its toxicity, the pyrrole structure of nitrogen-containing heterocyclic rings, some nitrogen-containing heterocyclic compounds are biologically active, or have an impact on organisms. Formamide groups cannot be ignored, and some formamide substances have been proven to be potentially harmful to organisms, or can cause cytotoxicity, genetic toxicity, etc. And the polycyclic aromatic hydrocarbons in the compound structure, such as naphthalene and structure, many polycyclic aromatic hydrocarbons have carcinogenic, teratogenic and mutagenic "three-induced" effects.

In summary, this "N- (1,3-naphthaleno-heterocyclopentene dioxide-5-methylphenyl) -3-chloro-6-methoxy-1-naphthaleno-pyrrole-2-formamide", due to its special molecular structure, or there are certain safety hazards and toxicity risks. When using and studying this compound, we should be careful and take careful precautions to further explore its impact on organisms and the environment.

What is the market price of N- (1,3-benzodioxane-5-ylmethyl) -3-chloro-6-methoxy-1-benzothiophene-2-formamide?

I don't know the price of "N- (1,3-naphthaleno-heterocycloheptane-5-methylphenyl dioxide) -3-chloro-6-methoxy-1-naphthalimidazole-2-formamide" as you said. This is a specific compound in the field of fine chemistry or pharmaceutical chemistry, and its price varies depending on many factors.

First, purity is the key factor. If the purity is very high, it is suitable for high-precision fields such as pharmaceutical research and development, and the price will be high; if the purity is slightly lower, it is used for general chemical research, and the price may be slightly reduced.

Second, market supply and demand also affect the price. If the demand for this compound is strong and the supply is limited, the merchant may raise the price; if the demand is weak, the supply exceeds the demand, and the price may decline.

Third, the difficulty of preparation is closely related to the cost. If the synthesis requires complex steps, expensive raw materials or special reaction conditions, the high cost will also be high; if the preparation is relatively simple, the cost is controllable, and the price may be close to the people.

Fourth, the production scale also plays a role. In large-scale production, due to the scale effect, the unit cost may be reduced, and the selling price may be more competitive; in small-scale production, the unit cost is high, and the price is also high.

To know the exact market price, you can consult chemical product suppliers, pharmaceutical raw material sellers, or check on professional chemical product trading platforms to obtain accurate prices.