Chemical Name | [3aR-(3aα,6α,7aβ)]-Hexahydro-8,8-dimethyl-3H-3a,6-methano-2,1-benzisothiazole 2,2-dioxide |
Molecular Formula | C12H19NO2S |
Molecular Weight | 241.35 |
Physical State | Solid (usually) |
Solubility In Water | Low (due to non - polar groups) |
Solubility In Organic Solvents | Moderate solubility in some organic solvents like chloroform, dichloromethane |
Appearance | White to off - white solid |
Odor | Odorless (usually) |
Vapor Pressure | Low (due to solid state) |
What is the chemical structure of [3aR- (3a α, 6α, 7a β) ] -hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide?
This is a very complex chemical structure description. To clarify the chemical structure of its 2,2-dioxide, it needs to be dissected step by step.
View "[3aR- (3aα, 6α, 7aβ) ] -octahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzisofuran", this part outlines a rather complex cyclic organic skeleton. Among them, 3aR indicates a specific three-dimensional configuration, and (3aα, 6α, 7aβ) further precisely defines the spatial orientation of specific atoms on the ring. Octahydro means that there are eight hydrogen atoms participating in the ring structure, and 8,8-dimethyl indicates that there are two methyl groups at position 8. 3H-3a, 6-methylene indicates that 3a and position 6 are connected by methylene, and 2,1-benzisofuran reveals that this ring structure is related to the benzisofuran structure.
On this basis, 2,2-dioxide is added, which means that at position 2 of the complex ring skeleton, two oxygen atoms are connected to form a dioxide structure. It can be speculated that in this dioxide structure, two oxygen atoms are connected with carbon atoms at position 2 by specific chemical bonds, which may form related structures such as peroxides and sulfones. Since more reaction conditions and surrounding atomic connection information are not provided, the approximate structure outline can only be inferred based on the existing nomenclature. However, the exact form of this structure needs to be combined with more spectral data, reaction mechanism and other information to be accurately determined.
What are the physical properties of [3aR- (3a α, 6α, 7a β) ] -hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide?
"Tiangong Kaiwu" says: "There are many physical properties of oxides.
Dioxides have different forms. Some are gaseous at room temperature, such as carbon dioxide, which is colorless and odorless, slightly denser than air, and soluble in water. Although this gas is invisible, it plays a great role in the world. It is a raw material for plant photosynthesis and is also related to the regulation of climate.
Furthermore, there are solid oxides, such as silica, which are commonly found in quartz and sand. It is hard and chemically stable, and is often an important raw material for construction and glass manufacturing.
And the melting and boiling points of dioxide are different. Some dioxide have a low melting and boiling point, which is volatile; while some have a very high melting and boiling point, which requires high temperature to change its shape.
In addition, solubility is also an important property. Some dioxide can react with water to form corresponding acids, such as sulfur dioxide dissolved in water to form sulfurous acid; while others are insoluble in water, such as manganese dioxide, which mostly exists in solid state in water and does not dissolve with water.
As for its conductivity, most dioxide is an insulator and does not have electrical conductivity. However, there are also special cases that can exhibit the properties of semiconductors under specific conditions.
The physical properties of dioxide, whether related to its molecular structure or affected by external conditions, are of great significance to the operation of all things in the world, the process of industrial production, and the needs of daily life.
What is the use of [3aR- (3a α, 6α, 7a β) ] -hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide?
2,2-Dioxide has a wide range of uses and plays a key role in many fields.
In the field of chemical synthesis, it is often used as a strong oxidizing agent. Due to its strong oxidizing ability, it can promote many oxidation reactions to proceed efficiently. For example, in organic synthesis, alcohols can be efficiently oxidized to aldehyde or carboxylic acid compounds. In the process of synthesizing fine chemicals such as specific drugs and fragrances, this property can accurately construct the target molecular structure, greatly improving the synthesis efficiency and product purity.
In the field of environmental protection, 2,2-Dioxide also makes important contributions. For example, in wastewater treatment, its oxidative properties can be used to decompose many harmful organic pollutants in wastewater, such as phenols, cyanides, etc., and convert them into harmless or less harmful substances to achieve the purpose of purifying water quality. And in air purification, it can react with some harmful gases, reduce the concentration of atmospheric pollutants, and help improve air quality.
In the field of materials science, 2,2-dioxide also shows unique value. When preparing high-performance polymer materials, adding an appropriate amount of this substance can effectively improve material properties, such as enhancing material thermal stability, mechanical strength, etc. During the preparation of some special ceramic materials, its participation can optimize the microstructure of ceramics and give materials better electrical and optical properties.
To sum up, 2,2-dioxide, with its unique chemical properties, plays an indispensable role in chemical synthesis, environmental protection, materials science and other fields. With the continuous advancement of science and technology, its use is expected to be further expanded and deepened.
What are the synthesis methods of [3aR- (3a α, 6α, 7a β) ] -hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide?
Guan Jun asked about the synthesis method of [3aR- (3aα, 6α, 7aβ) ] -octahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzisofuran-2,2-dioxide. This is the category of organic synthesis. The synthesis method is complicated and often depends on the existing raw materials, reaction conditions and target product characteristics.
First, it can be formed from suitable starting materials by carbon-carbon bonds, such as Diels-Alder reaction, to build the core skeleton. This reaction has the advantage of good stereoselectivity. If the raw materials are properly selected, intermediates with specific configurations can be efficiently obtained.
Second, functional group transformation is also the key. The desired functional group can be introduced or converted by oxidation, reduction, substitution and other reactions. If an appropriate oxidant is used, a specific group is oxidized to a dioxide structure.
Third, the protective group strategy is also often used. In the reaction process, in order to prevent sensitive groups from being affected, a protective group can be introduced, and the protective group can be removed after the specific reaction is completed.
Fourth, catalytic reactions are also powerful means. For example, metal catalytic reactions can promote the formation and transformation of specific chemical bonds, and improve the efficiency and selectivity of the reaction.
The path of organic synthesis requires repeated experiments, optimization, and comprehensive consideration of reaction conditions, yield, selectivity and many other factors in order to find an efficient and feasible synthesis path. The method of synthesis is not static, but relies on the wisdom and experience of organic synthesizers to continuously explore and innovate in order to achieve the synthesis of the target product.
[3aR- (3a α, 6α, 7a β) ] -Hexahydro-8,8-dimethyl-3H-3a, 6-methylene-2,1-benzoisothiazole 2,2-dioxide What are the precautions during use?
In the process of using dioxidizers, you need to pay attention to the following matters.
First, it is related to storage. Dioxidizers should be stored in a cool, dry and well-ventilated place, and must not be stored with flammable, explosive or reducing substances. Due to the active chemical nature of dioxidizers, if they come into contact with these substances, it is very likely to cause a violent chemical reaction, or even cause an explosion. For example, flammable substances such as sulfur and phosphorus are mixed with dioxidizers, and a little carelessness can lead to disaster.
Second, be careful when using them. When using dioxidizers, be sure to use clean and dry appliances to resolutely avoid impurities from mixing in. Because impurities may catalyze the decomposition of dioxidizers, causing their performance to change. During the use process, if the appliance is stained with impurities such as moisture, it may cause the dioxidizer to react in advance.
Third, the use environment cannot be ignored. Dioxidizers should be used in a well-ventilated environment to prevent the accumulation of harmful gases generated by their decomposition. If used in a closed space, the concentration of harmful gases will increase, which will not only endanger the user's health, but also may cause other safety problems.
Fourth, it is essential to control the dosage. Strictly control the dosage of dioxidizers according to actual needs, and do not use them in excess. Excessive use will not only cause waste, but also may cause the reaction to be too violent, making it difficult to control the reaction process and causing unnecessary danger.
Fifth, protective measures are essential. When using dioxidizers, it is necessary to take good personal protection, such as wearing protective gloves, goggles, masks, etc. Because it is corrosive and irritating, if it accidentally touches the skin or eyes, it will cause harm to the human body.
Only in the process of using dioxidizers, pay great attention to the above matters and strictly follow the relevant operating norms to ensure safe use and avoid accidents.