What is the chemical structure of 1- {2- [ (7-chloro-1-benzothiophen-3-yl) methoxy] -2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1)?

This is the chemical structure analysis of 1 - {2 - [ (7 - chloro - 1 - benzothiophene - 3 - yl) methoxy] -2 - (2,4 - dichlorophenyl) ethyl} -1H - imidazole nitrate (1:1). According to its name, this compound is based on 1H - imidazole. In the first position of imidazole, there is a complex side chain attached. The side chain starts with 2 - [ (7 - chloro - 1 - benzothiophene - 3 - yl) methoxy] -2 - (2,4 - dichlorophenyl) ethyl moiety. The 2 - position carbon atom is simultaneously connected with (7 - chloro - 1 - benzothiophene - 3 - yl) methoxy and 2,4 - dichlorophenyl. 7 - chloro - 1 - benzothiophene - 3 - group is connected to the main chain through methoxy group, and 2,4 - dichlorophenyl is directly connected to the 2 - position carbon of the main chain. Furthermore, the whole compound is combined with nitrate in a ratio of 1:1, which means that each of the above organic structural units is matched with a nitrate ion. In this way, the unique chemical structure of 1 - {2 - [ (7-chloro-1-benzothiophene-3-yl) methoxy] -2 - (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1) is formed.

What are the main physical properties of 1- {2- [ (7-chloro-1-benzothiophen-3-yl) methoxy] -2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1)?

1 - {2 - [ (7 - chloro - 1 - benzothiophene - 3 - yl) methoxy] - 2 - (2,4 - dichlorophenyl) ethyl} -1H - imidazole nitrate (1:1), this is an organic compound. Its main physical properties are as follows:

Looking at its morphology, it is mostly in a solid state at room temperature and pressure, but its specific crystal form may vary depending on the preparation method.

As for the color, it is usually white to off-white, but it may change slightly due to the mixing of impurities. < Br >
When it comes to melting point, because its molecular structure has a specific interaction, it has a fixed melting point, but the exact value is about a specific temperature range due to different experimental conditions or differences.

In terms of solubility, in organic solvents, it shows specific solubility characteristics. In common organic solvents such as dichloromethane, chloroform, etc., it has a certain solubility. Because the molecular structure of the compound contains lipophilic parts, it can form interactions with organic solvent molecules. However, in water, the solubility is low, because the overall hydrophobic properties of the molecule are strong, and the interaction between water molecules and it is weak. < Br >
Density is also one of its important physical properties. Although the exact value needs to be determined experimentally and accurately, according to the laws of its molecular composition and similar compounds, it can be inferred that its density is within a certain range, which is related to its molecular mass and molecular accumulation method.

In addition, the compound may have certain stability and can maintain its own structure intact under conventional environmental conditions. In case of extreme conditions such as high temperature, strong acid, and strong base, the molecular structure may change, causing its physical properties to also change.

What is the synthesis method of 1- {2- [ (7-chloro-1-benzothiophen-3-yl) methoxy] -2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1)?

To prepare 1-% 7B2-% 5B% 287-chloro-1-benzothiophene-3-yl% 29 methoxy% 5D-2 - (2,4-dichlorophenyl) ethyl% 7D-1H-imidazole nitrate (1:1), the method is as follows:
First take 7-chloro-1-benzothiophene-3-methanol and react with appropriate reagents to convert its hydroxyl group into an active leaving group for subsequent nucleophilic substitution reaction. This step requires the reaction of halogenated reagents in a suitable solvent under mild heating and alkali catalysis to generate the corresponding halogenated compound. < Br > Simultaneously, 2 - (2,4 - dichlorophenyl) acetaldehyde was prepared. It can be obtained by 2,4 - dichlorobenzene and corresponding aldehyde-based reagents under specific catalysts and reaction conditions.
The above generated 7-chloro-1-benzothiophene-3-halomethane is mixed with 2- (2,4-dichlorophenyl) acetaldehyde in an alkaline environment and an organic solvent to promote the nucleophilic addition reaction to form the key intermediate 2 -% 5B% 287 - chloro-1 - benzothiophene-3 - yl% 29 methoxy% 5D - 2 - (2,4 - dichlorophenyl) ethanol.
Subsequently, this intermediate is reacted with 1H-imidazole under dehydrating agent and suitable temperature and pressure conditions to construct the imidazole structural part of the target molecule. The reaction process needs to be closely monitored to prevent side reactions.
Finally, the resulting product is reacted with nitric acid in suitable solvents and reaction conditions to form 1-% 7B2-% 5B% 287-chloro-1-benzothiophene-3-yl% 29 methoxy% 5D-2 - (2,4-dichlorophenyl) ethyl% 7D-1H-imidazole nitrate (1:1). After the reaction is completed, the target product with high purity can be obtained through extraction, crystallization, recrystallization and other purification steps. The whole synthesis process requires strict control of reaction conditions and fine operation to ensure product yield and purity.

1- {2- [ (7-chloro-1-benzothiophen-3-yl) methoxy] -2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1) is used in what fields?

1-% {2- [ (7-chloro-1-benzothiophene-3-yl) methoxy] -2 - (2,4-dichlorophenyl) ethyl} -1H -imidazolium nitrate (1:1) This compound has many wonderful functions in the field of medicine. It has remarkable effects in the field of antifungal. Many fungal infections, such as dermatophytosis caused by dermatophytosis, or visceral infections caused by candida, are often effective when used as medicine. Due to its unique molecular structure, it can precisely act on specific targets of fungal cells, interfere with their normal physiological metabolism, and then inhibit fungal growth and reproduction.

In the context of agriculture, it also has considerable applications. In response to fungal diseases suffered by crops, the application of agents containing this compound can effectively prevent and control, protect crops from thriving and ensure the hope of a bumper harvest. For example, after harvest preservation of fruits and vegetables, spraying related preparations can prolong their shelf life and reduce the loss caused by fungal spoilage.

Furthermore, in the field of scientific research, it is an important research tool. By exploring the mechanism of its interaction with fungi, researchers can deepen their understanding of fungal physiological characteristics, lay a solid theoretical foundation for the development of better antifungal drugs. It also helps to reveal the complex biochemical reaction pathways in organisms and expand the boundaries of life science.

How safe is 1- {2- [ (7-chloro-1-benzothiophen-3-yl) methoxy] -2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1)?

Looking at this product named 1- {2- [ (7-chloro-1-benzothiophene-3-yl) methoxy] -2- (2,4-dichlorophenyl) ethyl} -1H-imidazole nitrate (1:1), its safety considerations are quite complex. In terms of chemical nature, this compound has a unique structure and coexists with multiple halogen atoms, which may affect its chemical stability and reactivity. In terms of environmental safety, if it flows into nature, it may be hindered by its complex structure, or accumulate in the ecosystem, endangering the biological community.

In toxicology, although there is no detailed conclusion, halogen-containing organic structures often have potential toxicity, or damage human organs, and interfere with physiological functions. Acute toxicity or discomfort to contacts, chronic exposure risk cannot be ignored, or there is a risk of carcinogenesis, teratogenesis, and mutation.

Re-discuss operation safety, production and use processes must be cautious. Because of its chemical activity, improper operation or chemical reaction can cause runaway, causing safety accidents. And potentially toxic, the operation field needs complete protection to prevent inhalation and contact.

Transportation and storage are also critical. According to the regulations on hazardous chemicals, suitable packaging must be selected to prevent leakage and deterioration. The storage environment needs to be strictly controlled for temperature and humidity, away from fire sources, oxidants, etc., to avoid reaction risks.

In summary, there are many uncertainties in the safety of this compound, which requires in-depth research and evaluation, and careful treatment in all aspects to ensure human health and environmental safety.