6 Ethoxy 2 2 4 Trimethyl 1 2 Dihydroquinoline
Quinoline Thiophene Imidazole Thiazole
6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline
Chemical Formula C14H21NO
Molecular Weight 217.32 g/mol
Appearance usually a solid
Color light - colored (e.g., white to pale yellow)
Odor characteristic organic odor
Melting Point around 70 - 75 °C
Boiling Point 310 - 314 °C
Solubility In Water poorly soluble
Solubility In Organic Solvents soluble in common organic solvents like ethanol, toluene
Density approx. 1.02 g/cm³
FAQ

What is the chemical structure of 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline?

6-Ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline, which is one of the organic compounds. Looking at its naming, it is analyzed according to the naming rules of organic chemistry.

"Quinoline" is a kind of nitrogen-containing heterocyclic parent nucleus structure with a typical benzopyridine skeleton. And "1,2-dihydro" is clearly shown in the state of double bond hydrogenation between the 1 and 2 positions of the quinoline parent nucleus, which has a great influence on its electron cloud distribution and chemical activity.

"2,2,4-trimethyl" indicates that there are two methyl groups at the 2nd position of the quinoline ring and one methyl group at the 4th position. The introduction of methyl groups can change the electron cloud density of molecules, affecting their chemical reactivity and physical properties, such as boiling point, solubility, etc.

"6-ethoxy", which means that the 6-position of the quinoline ring is replaced by ethoxy (-O - CH - CH). Ethoxy groups are also supply subgroups, and have a slightly stronger power supply than methyl groups, which has a greater impact on the electronic effects of molecules. Its steric resistance also changes the spatial structure of molecules, which in turn affects their interactions with other molecules.

In summary, the chemical structure of 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline, with quinoline as the parent nucleus, is modified by dihydrogenation, methyl and ethoxy substitution. This unique structure endows it with specific chemical and physical properties and may have specific uses in organic synthesis, materials science and other fields.

What are the physical properties of 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline?

6-Ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline is one of the organic compounds. Its physical properties are quite unique, let me tell them one by one.

When it comes to appearance, under room temperature and pressure, it is mostly a transparent liquid with a light yellow to amber color. The texture is relatively uniform, and no obvious impurities are visible. The appearance is quite shiny, just like the essence of precipitation over time.

As for its smell, it has a special aromatic smell, which is neither rich and pungent nor light. This smell is unique among organic compounds and has high recognition. The boiling point of

is between 267 and 275 degrees Celsius. Under this temperature condition, the substance will change from liquid to gaseous state. This characteristic is crucial in the process of industrial distillation and separation. It is necessary to precisely control the temperature to ensure the purity and efficiency of its separation.

In terms of melting point, it is roughly around -15 degrees Celsius, which means that the temperature drops below this point, and the compound will solidify from liquid to solid state, like a sleeping spirit, waiting for the appropriate temperature to wake up again and show its liquid agility. < Br >
The density is about 0.996 - 1.006g/cm ³, which is slightly heavier than water. When placed in water, it will slowly sink. This density characteristic is one of the important factors to consider in experiments and industrial applications such as substance mixing and stratification.

In terms of solubility, this compound is soluble in many organic solvents, such as ethanol, acetone, benzene, etc., but its solubility in water is relatively low. This property allows it to be effectively separated and purified according to the different characteristics of solvents in chemical synthesis, extraction, etc.

The physical properties of 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline are of great significance in the chemical industry, scientific research and other fields. In-depth study of its characteristics can be used in related applications to maximize its effectiveness.

What are the common uses of 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline?

6-Ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline, this is an organic compound. Its common use is mostly related to the field of rubber additives.

In the rubber industry, it is often used as an antioxidant. Because rubber products are susceptible to aging under the influence of environmental factors such as air, heat and light, resulting in performance deterioration. This compound can effectively delay the aging process of rubber and greatly extend the service life of rubber products. Its mechanism of action is to capture free radicals generated during the aging process of rubber by virtue of its own structural characteristics, block chain reactions, and achieve the purpose of protection.

In tire manufacturing, this substance is widely used. During the driving process, tires are frequently subjected to friction, heat and oxidation, and are prone to aging. After adding this compound, the anti-aging properties of tires can be significantly improved, ensuring that tires can maintain good physical properties and safety under long-term use and different working conditions.

In addition, in the production of other rubber products, such as hoses, tapes, seals, etc., 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline also plays a key anti-aging role, helping to maintain the quality and performance stability of products, thereby meeting various industrial and civilian needs.

What are the synthesis methods of 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline?

The synthesis method of 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline is an important matter in the field of chemical preparation. Its synthesis method has been studied by many scholars in the past, and it is described as follows.

First, it can be achieved through a specific organic reaction path. Starting with the corresponding quinoline-containing precursor structure, under suitable reaction conditions, ethoxy and methyl groups are introduced. Among them, the reaction temperature, reaction time and the ratio of reactants need to be carefully regulated. If the temperature is too high, or side reactions occur frequently, the purity of the product is damaged; if the temperature is too low, the reaction rate is slow and takes a long time. And whether the ratio of the reactants is accurate or not also affects the yield of the product.

Second, the choice of catalyst is crucial. Appropriate catalysts can significantly improve the reaction rate and selectivity. Or use metal catalysts to promote the reaction with their unique electronic structure and catalytic activity. However, when using metal catalysts, attention should be paid to the recovery and reuse of catalysts to reduce costs and conform to the concept of green chemistry.

Third, the choice of reaction solvent should not be underestimated. Different solvents have an impact on the solubility and reactivity of the reactants. Choose a polar solvent or a non-polar solvent, depending on the specific reaction mechanism and the characteristics of the reactants. Polar solvents may enhance the solubility of ionic reactants and promote the reaction; non-polar solvents are more advantageous in the reaction of some non-polar reactants.

All these synthesis methods have their own advantages and disadvantages. In actual operation, it is necessary to weigh the cost, yield, purity and many other factors, and make careful choices to achieve the best synthesis effect.

What are the precautions for using 6-ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline?

6-Ethoxy-2,2,4-trimethyl-1,2-dihydroquinoline, this is an organic compound. During use, many precautions should be kept in mind.

Bear the brunt, safety protection is essential. This compound may have certain toxicity and irritation, and it is necessary to take protective measures when contacting it. Operators should wear protective clothing, protective gloves and goggles to avoid direct contact with the skin and prevent eye damage. If accidentally touching the skin, rinse immediately with plenty of water; if splashing into the eyes, rinse quickly with plenty of running water and seek medical attention in time.

Furthermore, the compound is also exquisite in storage. It should be stored in a cool and well-ventilated place, away from fire and heat sources. Because it is flammable, it is easy to burn in case of open flames and hot topics, so the temperature and fire source control of the storage environment must not be neglected. At the same time, it should be stored separately from oxidants and acids, and do not mix them to prevent dangerous chemical reactions.

During use, the ventilation conditions of the operating environment must be good. Because of its volatile gases or harmful to the human body, good ventilation can discharge harmful gases in time, reduce the concentration in the air, and protect the health of the operator. And when operating, strictly abide by the operating procedures, do not eat, drink water or smoke in the operating area to prevent harmful substances from entering the human body through the mouth.

In addition, the amount and scope of use of the compound should also be strictly controlled. Precisely weigh and take according to actual needs to avoid waste, and do not use beyond the range to prevent unnecessary harm to the environment and human body. After use, properly dispose of the remaining materials and waste, follow relevant environmental protection regulations, and do not discard them at will.