1,2-Dichloroethylene has two isomers, cis and trans, with different properties, and its main uses are quite extensive.
In the field of chemical synthesis, 1,2-dichloroethylene is a key organic synthesis raw material. It can be converted into important compounds such as vinyl chloride through a series of chemical reactions. Vinyl chloride is a monomer for synthesizing polyvinyl chloride (PVC), and PVC is widely used in building materials, packaging materials, daily necessities, etc., such as common plastic pipes, plastic doors and windows and other building materials, as well as various plastic products. Tracing its origin, 1,2-dichloroethylene plays an important role as a starting material in its synthesis chain.
In the field of organic solvents, 1,2-dichloroethylene has become a choice for organic solvents due to its good solubility. It can dissolve many organic substances. In the paint, ink, adhesive and other industries, it can be used to dissolve resins, pigments and other ingredients to adjust the viscosity and coating performance of products. For example, in the production of coatings, the appropriate amount of 1,2-dichloroethylene can make the coating more evenly applied to the surface of the object, forming a flat and smooth coating, and improving the decorative and protective effect of the coating.
In addition, 1,2-dichloroethylene can also be used as a reaction medium in some specific chemical reactions. Due to its relatively stable chemical properties, it can provide a suitable environment for chemical reactions, promote the smooth progress of the reaction, and ensure the selectivity and yield of the reaction.
However, it should be noted that 1,2-dichloroethylene has certain toxicity, and strict safety specifications and operating procedures should be followed during use to ensure the safety of personnel and the environment from pollution.

1% 2C2-diethyl ether, also known as ethoxyethane, is a kind of organic compound. Although "Tiangong Kaiwu" does not directly describe 1% 2C2-diethyl ether, it can be described according to the common descriptions of physical properties and chemical substances by the ancients, and its physical properties can be expressed in the style of ancient classical Chinese.
1% 2C2-diethyl ether, at room temperature, is a colorless and clear liquid. It looks like clear water, transparent and free of variegation. Under sunlight, it shimmers shimmeringly, like flowing glaze. Its gas is specific, fragrant and volatile. When it is smelled, it has a unique fragrance at first, but when it is smelled for a long time, it feels pungent and uncomfortable.
In terms of its density, it is lighter than water. If it is poured into water, it will float on the water surface. It is like oil dripping on water, not fusing with each other, forming a layer of its own. Its boiling point is quite low, about 34.6 ° C. After a little heating, it quickly vaporizes into steam and rises in the air, like the curl of mist.
1% 2C2-diethyl ether is very easy to burn. In case of open flame or hot topic, it will explode instantly. The flame is light blue, bright and hot. When burning, it is accompanied by thick smoke rising. Its steam and air can form an explosive mixture, and in a limited space, it is at risk of violent explosion in case of fire.
Furthermore, 1% 2C2-diethyl ether is an excellent organic solvent, which can dissolve many organic substances, such as oils, resins, etc., so that they can be dispersed in it to form a uniform mixing system. Although there are no clear application examples in ancient times, it is deduced from today's chemical principles. If the ancients observed it, it may be used to extract some insoluble substances, and it may be useful in process production.

1% 2C2-divinylbenzene is an organic compound with unique chemical properties. This substance contains unsaturated double bonds, so it is chemically active and easily participates in various addition reactions.
Looking at its structure, the benzene ring is conjugated with the double bond, giving it a special electron cloud distribution. Due to the conjugation effect, the stability of 1% 2C2-divinylbenzene is improved, but the existence of the double bond still makes it highly reactive.
In addition reactions, the double bond can interact with many electrophilic reagents or nucleophiles. If added with halogens, halogen atoms can be added to the double bond to form halogens. It can also be hydrogenated with hydrogen under the action of a catalyst to saturate the double bond to form the corresponding saturated hydrocarbon derivatives.
1% 2C2-divinylbenzene can still be polymerized. With its two double bonds, it can be polymerized by free radical polymerization or ionic polymerization to form a polymer. Such polymers are widely used in the field of materials science, such as the preparation of ion exchange resins, adsorption resins, etc., all rely on the polymerization properties of 1% 2C2-divinylbenzene.
In addition, 1% 2C2-divinylbenzene can also participate in the substitution reaction. The hydrogen atom on the styrene ring can be replaced by other groups under appropriate conditions, thereby deriving a variety of derivatives and expanding its application range. Overall, the unique structure of 1% 2C2-divinylbenzene has both active reactivity and special stability, and it has important location and wide application prospects in many fields such as organic synthesis and material preparation.

1% 2C2-divinylbenzene is a colorless liquid and is often used as a crosslinking agent for synthetic resins, ion exchange resins, and rubbers. Although its preparation method is difficult to trace in ancient records, according to today's chemical process knowledge, it can be made as follows:
First, ethylene and benzene are used as raw materials and reacted under the action of a catalyst. This process requires specific reaction conditions, such as suitable temperature and pressure. Metal halide is usually used as a catalyst to promote the addition reaction of ethylene and benzene to form ethylbenzene, and then ethylbenzene is further reacted with ethylene under specific conditions to gradually form 1% 2C2-divinylbenzene. The raw materials of this method are easy to obtain, but the reaction steps are slightly complicated. It is necessary to precisely control the reaction conditions in order to improve the purity and yield of the product.
Second, it is prepared from the dehydrogenation of diethylbenzene. Under the action of the dehydrogenation catalyst, diethylbenzene removes hydrogen atoms and converts to 1% 2C2-divinylbenzene. The key to this process is to choose high-efficiency dehydrogenation catalysts, such as iron-based and chromium-based catalysts. At the same time, factors such as reaction temperature, pressure and feed speed have a great influence on the reaction. Although high temperature is conducive to the dehydrogenation reaction, it may trigger side reactions and reduce the selectivity of the product. Therefore, it is necessary to fine-tune the reaction parameters to achieve the best reaction effect.
Third, it is prepared by Halogenated benzene reacts with magnesium to form Grignard reagent, and then reacts with vinyl halide. After a series of complex organic synthesis steps, 1% 2C2-divinylbenzene can be obtained. This method requires high equipment and operation, and needs to be carried out under harsh conditions without water and oxygen, and the reagents used are relatively expensive and relatively expensive. However, this method can achieve precise control of the product structure, which is quite advantageous in specific needs.

For 1% 2C2-divinylbenzene, there are all kinds of things that should be paid attention to when it is hidden and transported.
When hiding, place the most importance on it. It should be placed in a cool and well-ventilated place to avoid open fires and hot topics. This substance is flammable, and it is prone to disasters and risks of fire in case of fire. The temperature of the warehouse should also be carefully controlled and should not be too high to prevent changes in material properties and risks of safety.
Furthermore, sealing is also critical. Make sure that the container containing 1% 2C2-divinylbenzene is tight to prevent it from excessive contact with the air. Due to its lively nature, it can be in contact with the air for a long time, or cause chemical reactions such as oxidation, which can damage its quality and generate harmful substances.
When transporting, there are also many important rules. The person handling it must be careful to avoid falling and heavy pressure. The container of this substance may be broken due to excessive external force, resulting in leakage of 1% 2C2-divinylbenzene. After leakage, it will not only pollute the environment, but also cause poisoning and other harmful things to human health due to volatile gases.
Vehicles used for transportation also need to be specially disposed of. Fire and explosion-proof facilities should be provided, and it should be clean and free of debris to avoid adverse reactions with 1% 2C2-divinylbenzene. During driving, drivers should also be cautious, avoid bumpy roads, drive at a steady speed, and ensure the safety of transportation.
In addition, regardless of storage or transportation, relevant personnel should be familiar with the characteristics of 1% 2C2-divinylbenzene and emergency measures. In case of leakage, etc., effective measures can be taken quickly to minimize the damage. In this way, the process of storing and transporting 1% 2C2-divinylbenzene can be guaranteed to be smooth and avoid accidents.