1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E7%9A%84%E4%B8%BB%E8%A6%81%E7%94%A8%E9%80%94%E5%A6%82%E4%B8%8B%EF%BC%9A
This compound is often used as a key intermediate in the synthesis of a variety of drug molecules with specific biological activities in the field of medicinal chemistry. Due to its unique chemical structure, it can interact with specific targets in organisms, helping to develop innovative drugs for the treatment of various diseases such as inflammation and tumors.
In the field of materials science, 1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E7%9A%84 special structure endows it with potential photoelectric properties. It can be used to prepare new organic photoelectric materials, such as organic Light Emitting Diode (OLED), organic solar cells, etc., which are expected to improve the photoelectric conversion efficiency and stability of these materials.
In the field of organic synthetic chemistry, it is an extremely important building block. With its three specific sites of active groups, complex organic molecular structures can be constructed through a variety of organic reactions, such as substitution reactions, addition reactions, etc., providing organic synthesis chemists with rich strategies and possibilities to help expand the structural diversity of organic compounds and promote the development and innovation of organic synthetic chemistry.
In short, 1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E7%9A%84 plays an indispensable role in many important scientific fields, and is of key significance to the progress of scientific research and the expansion of practical applications in related fields.

1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E5%A6%82%E4%B8%8B%E6%89%80%E8%BF%B0:
The outer surface of this compound is often black to blue, with a special smell. Its melting temperature is low, around -60 ° C, which makes it liquid in normal environments. The boiling temperature is high, probably around 200-220 ° C. This characteristic makes it able to maintain the physical stability of the phase at a certain degree of temperature.
In terms of density, the 1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E7%9A%84 density is slightly higher than that of water, < 1.0-1.1 g/cm ³, which means that it will sink in water. In terms of solubility, the compound is soluble in water, and it is soluble in water, such as ethanol, ether, etc. This is because it is soluble. The molecular force is more compatible, and it conforms to the principle of similar miscibility.
Its chemical properties are low, and it is not easy to quickly dissipate under normal conditions. In addition, the chemical properties have a certain degree of certainty, and in general conditions, the chemical properties are determined, and it is not easy to produce strong reactions. However, in the presence of specific materials, such as high temperature, acid, acid or catalyst, it may also lead to chemical reactions and exhibit different chemical activities. In addition, the physical nature of 1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF makes it have a specific value in multiple domains, and also lays the foundation for its chemical reactions.

1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E7%9A%84%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%E5%9D%A6%E7%A8%B3%E5%AE%9A%E4%B9%8B%E7%89%A9. Among this substance, its molecular structure is unique, and the structure of tri (triethoxy methyl) benzene makes its chemical activity subtle.
From the perspective of chemical bonds, the benzene ring is a stable conjugated system, and the triethoxy methyl group connected to it is connected to the benzene ring by a carbon-oxygen bond. This carbon-oxygen bond has a certain polarity, resulting in different electron cloud distributions. However, due to the conjugation effect of the benzene ring, its chemical stability can still be preserved.
In common chemical environments, if the temperature does not reach a certain threshold and there is no strong chemical agent intervention, this substance can maintain a relatively stable state. It has a certain tolerance to the general weak acid-base environment, just like the city wall to resist the invasion of ordinary wind and rain.
When encountering strong oxidants, the carbon-hydrogen bonds on the ethoxy methyl group can be oxidized or cause structural changes. In the case of high temperature and the presence of special catalysts, the substituents on the benzene ring may undergo reactions such as rearrangement, and the stability will be destroyed.
In summary, 1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF most common conditions, the chemical properties are relatively stable, but in extreme or special chemical environments, the stability may be challenged.

1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E7%9A%84%E5%90%88%E6%88%90%E6%96%B9%E6%B3%95%E6%9C%89%E4%B8%8B%E5%88%97%E5%87%A0%E7%A7%8D%EF%BC%9A
- **%E4%BB%A5%E4%B8%89%E6%B0%9F%E7%94%B2%E9%85%8D%E4%BD%93%E4%B8%BA%E5%8E%9F%E6%9D%90%E7%9A%84%E6%96%B9%E6%B3%95**
- **%E5%85%88%E5%88%9B%E5%BB%BA%E4%B8%89%E6%B0%9F%E7%94%B2%E7%9A%84%E5%9F%BA%E7%A1%80%E5%8D%95%E5%85%83**: The Grignard reagent can be prepared by the reaction of halogenated ethane and magnesium in anhydrous ether, such as $C_2H_5Br + Mg\ xrightarrow [] {anhydrous ether} C_2H_5MgBr $. The Grignard reagent can be reacted with formaldehyde to introduce a hydroxyethyl group, and then the ethanol derivative is obtained by subsequent treatment, and then the halogenated ethanol derivative is obtained by halogenation reaction. After that, the halogenated ethanol derivative can be reacted with magnesium to obtain a new Grignard reagent, and then reacted with ethylene oxide to increase the carbon chain and introduce suitable functional groups. After multi-step reaction treatment, a compound containing three hydroxyethyl groups is obtained.
- **%E7%94%A8%E5%85%B6%E4%B8%8E%E8%8B%AF%E9%85%8D%E4%BD%93%E5%8F%8D%E5%BA%94**: Under suitable reaction conditions, such as alkali catalysis, the obtained compound containing three hydroxyethyl groups undergoes condensation reaction with benzaldehyde or its derivatives. The base can capture the active hydrogen in the compound to form carbon negative ions, and then undergo nucleophilic addition reaction with the carbonyl group of benzaldehyde. After dehydration and other steps, the final 1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF is formed.
- **%E4%BB%A5%E5%85%B6%E4%BB%96%E7%94%B2%E5%9F%BA%E5%8D%95%E5%85%83%E5%88%9B%E5%BB%BA%E5%90%8E%E7%BB%84%E5%90%88%E7%9A%84%E6%96%B9%E6%B3%95**
- **%E9%80%9A%E8%BF%87%E7%94%B2%E5%9F%BA%E5%8D%95%E5%85%83%E7%9A%84%E5%8F%8D%E5%BA%94%E6%9E%84%E5%BB%BA%E9%93%BE%E6%AE%B5**: Halogenated methane is used as the starting material and reacts with metal zinc to form organozinc reagents, such as $CH_3I + Zn\ xrightarrow [] {suitable conditions} CH_3ZnI $. The organozinc reagent reacts with carbonyl-containing compounds to grow carbon chains. Through a multi-step similar reaction, a suitable carbon chain structure containing three ethyl groups is gradually constructed.
- **%E8%8B%AF%E7%9A%84%E5%90%88%E6%88%90%E4%B8%8E%E7%BB%93%E5%90%88**: The constructed carbon chain structure containing three ethyl groups is reacted with the benzene ring under suitable conditions. For example, under the catalysis of Lewis acid, through the Fu-gram reaction, etc., the carbon chain structure is connected to the benzene ring, and after appropriate functional group transformation and modification, the final 1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF is obtained.

1%2C3%2C5-%E4%B8%89%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E8%8B%AF%E8%80%85 are organic compounds, and many matters need to be carefully paid attention to during storage and transportation.
Its chemical properties are lively, and it is easy to cause combustion or even explosion when exposed to heat, open flame or oxidant. Therefore, when storing, it should be placed in a cool and ventilated warehouse, away from fire and heat sources, and stored separately from oxidants and acids, and must not be mixed. The lighting, ventilation and other facilities of the warehouse must be explosion-proof. The switch should be located outside the warehouse, and there should be corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment.
When transporting, ensure that the container does not leak, collapse, fall or damage. The transportation vehicle should be equipped with the corresponding variety and quantity of fire-fighting equipment and leakage emergency treatment equipment. Summer transportation should be carried out in the morning and evening to avoid sun exposure. Road transportation should be carried out according to the specified route, and do not stop in residential areas and densely populated areas. When transporting by rail, it is forbidden to slip.
In addition, this compound may have certain toxicity and irritation, which can cause harm to human health. Storage and transportation personnel should take protective measures, such as wearing protective gloves, masks, goggles, etc., to prevent contact and inhalation. In the event of a leak, personnel from the contaminated area of the leak should be quickly evacuated to a safe area and quarantined to strictly restrict access. Emergency personnel must wear protective equipment and do not directly contact the leak. When a small amount of leakage occurs, it can be absorbed by inert materials such as sand and vermiculite. When a large amount of leakage occurs, a dike is built or a pit is dug for containment, covered with foam to reduce steam hazards, and then transferred to a tanker or a special collector with an explosion-proof pump for recycling or transportation to a waste treatment site for disposal.