Chemical Formula | C10H10F4O2 |
Molecular Weight | 236.18 |
Appearance | Typically a colorless to light - yellow liquid |
Boiling Point | Around 206 - 208 °C |
Density | Approx. 1.25 - 1.3 g/cm³ |
Solubility | Slightly soluble in water, soluble in organic solvents like ethanol, ether |
Vapor Pressure | Low at room temperature |
Flash Point | Around 78 - 80 °C |
Refractive Index | Typically around 1.44 - 1.46 |
Chemical Formula | C10H10F4O2 |
Molecular Weight | 236.18 |
Appearance | Colorless to light yellow liquid |
Boiling Point | Around 200 - 210 °C |
Density | Approx. 1.2 - 1.3 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in many organic solvents like ethanol, acetone |
Vapor Pressure | Low at room temperature |
Flash Point | Around 70 - 80 °C |
Chemical Formula | C10H10F4O2 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 198 - 200 °C |
Melting Point | N/A |
Density | 1.23 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Vapor Pressure | Low |
Flash Point | 78 °C |
Stability | Stable under normal conditions |
Hazardous Nature | Harmful if swallowed, inhaled or in contact with skin |
What are the main uses of 1,4-diethoxytetrafluorobenzene?
1,4-Diethoxytetrahydronaphthalene has a wide range of uses. In the field of organic synthesis, it is often an important intermediate. Due to its unique chemical structure, it can be derived from many organic compounds through various chemical reactions. For example, more complex organic molecular structures can be constructed through nucleophilic substitution reactions in which it participates, which is of great significance in pharmaceutical chemistry and materials science.
In the process of drug development, 1,4-diethoxytetrahydronaphthalene also has important functions. Its structural properties may endow the prepared drug with specific biological activities, or help to improve the solubility and stability of the drug. Therefore, when developing new drugs, chemists often use this as the base material and modify it, hoping to obtain new drugs with good curative effect and small side effects.
Furthermore, in the field of materials science, materials made from this raw material may have special electrical, optical or mechanical properties. For example, in the field of organic optoelectronic materials, through rational design and synthesis, materials that respond well to light and electricity may be prepared for the manufacture of Light Emitting Diodes, solar cells and other devices.
In addition, 1,4-diethoxytetrahydronaphthalene has also emerged in the fragrance industry. Due to its unique odor characteristics, it can be used to produce various flavors and fragrances, adding a unique aroma to the product and enhancing its quality and market competitiveness.
What are the physical properties of 1,4-diethoxytetrafluorobenzene?
1% 2C4-diethoxytetrahydronaphthalene is one of the organic compounds. Its physical properties are quite unique, let me describe them in detail for you.
Looking at its appearance, under room temperature and pressure, 1% 2C4-diethoxytetrahydronaphthalene is mostly colorless to light yellow liquid, clear and translucent, like a clear spring, without the disturbance of impurities, showing a pure state.
As for its smell, it often has a weak and special aromatic smell. Although this aroma is not rich and pungent, it has a unique charm. It seems to be absent, lingering at the nose end, attracting people to explore its mysteries. < Br >
Discusses the boiling point, which is about a specific temperature range. This temperature is the key node for the transformation of a substance from a liquid state to a gaseous state. The value of the boiling point is determined by many factors, such as the strength of the intermolecular forces. The boiling point of 1% 2C4-diethoxytetrahydronaphthalene makes it possible to realize the transformation of liquid and gas states at the corresponding temperature conditions. This property is of great significance in the separation, purification and other operations in the chemical industry.
The melting point is the temperature limit for the transformation of a substance from a solid state to a liquid state. The melting point of 1% 2C4-diethoxytetrahydronaphthalene is in a certain range. When it is lower than the melting point, it exists in a solid state and has a stable structure. When the temperature rises above the melting point, it gradually melts into a liquid state, showing a flowing state.
Its density is also one of the important physical properties. The density reflects the mass of the substance per unit volume, and the density of 1% 2C4-diethoxytetrahydronaphthalene is specific. This can be used in relevant calculations and practical applications to accurately grasp its dosage and occupied space.
In terms of solubility, 1% 2C4-diethoxy tetrahydronaphthalene has a certain solubility in organic solvents, and can dissolve with organic solvents such as ethanol and ether, just like fish and water. However, its solubility in water is relatively limited, which determines its behavior in different solvent systems. It plays a key guiding role in chemical synthesis, extraction and other processes.
In addition, the volatility of 1% 2C4-diethoxy tetrahydronaphthalene is relatively moderate, neither extremely volatile and instantly disappears, nor difficult to volatilize and long-term retention. This moderate volatility can be used in the application of coatings, inks and other industries, and process parameters such as drying speed can be skillfully adjusted to achieve the desired product effect.
In summary, the physical properties of 1% 2C4-diethoxy tetrahydronaphthalene are rich and diverse, and the properties are interrelated and affect each other. They play an indispensable and important role in many fields such as chemical industry and materials, and contribute unique value to human production and life.
Is the chemical properties of 1,4-diethoxytetrafluorobenzene stable?
The chemical properties of 1,4-diethoxy tetrahydronaphthalene are quite stable. This substance contains the structure of diethoxy and tetrahydronaphthalene, and diethoxy can increase its stability. The ethoxy group has the effect of donating electricity, which can make the distribution of molecular electron clouds more uniform and reduce the reactivity. The saturated structure of the tetrahydronaphthalene ring also stabilizes its chemical properties.
According to the principle of organic chemistry, such structures are less likely to initiate reactions. Such as unsaturated bonds of alkenes and alkynes, or carbonyl groups of aldodes and ketones, can promote the rapid initiation of the reaction. However, 1,4-diethoxy tetrahydronaphthalene does not have such active groups, and it is difficult to react violently with common reagents at room temperature and pressure. < Br >
And the ether bond is stable under normal conditions, and the diethoxy ether bond is difficult to break in the absence of special catalysts or extreme conditions. This stability makes 1,4-diethoxy tetralin less prone to deterioration during storage and use.
In summary, the chemical properties of 1,4-diethoxy tetralin are relatively stable. If there is no special environment and reagents, its structure is not easy to change, and it can be stored with peace of mind.
What are the preparation methods of 1,4-diethoxytetrafluorobenzene?
For 1% 2C4-diethoxy tetrahydronaphthalene, there are several ways to prepare it.
One method starts with naphthalene and first encounters with ethoxylating reagents. Naphthalene is active and can be introduced into ethoxy groups by combining with ethoxylating agents under appropriate conditions. If diethyl sulfate is used as ethoxylating agent, in an alkaline environment, naphthalene reacts with it and undergoes a process of nucleophilic substitution to obtain a precursor of 1% 2C4-diethoxy tetrahydronaphthalene. Then, the precursor is hydrogenated, and the naphthalene ring is partially hydrogenated in a hydrogen atmosphere with a suitable catalyst, such as palladium carbon, to form 1% 2C4-diethoxy tetrahydronaphthalene.
Another method starts from tetrahydronaphthalene. Tetrahydronaphthalene is first halogenated by introducing halogen atoms. If bromine is used as a halogenating agent, when light or catalyst exists, tetrahydronaphthalene can react with bromine to obtain halogenated tetrahydronaphthalene. After that, the halogenated tetrahydronaphthalene is reacted with ethoxylating reagents such as sodium ethanol, and nucleophilic substitution is used to replace halogen with ethoxy to obtain 1% 2C4-diethoxy tetrahydronaphthalene. < Br >
In addition, the desired structure can be gradually constructed from suitable aromatic derivatives through multi-step reactions. First, the aromatic derivatives are alkylated or acylated by Fu-gram, and ethoxy-containing groups are introduced. After a series of reactions such as reduction and cyclization, 1% 2C4-diethoxy tetralin is finally prepared. Each method has its own advantages and disadvantages. When preparing, it should be selected according to many factors such as the availability of raw materials, the level of cost, and the advantages and disadvantages of yield.
What are the precautions for storing and transporting 1,4-diethoxytetrafluorobenzene?
1%2C4-%E4%BA%8C%E4%B9%99%E6%B0%A7%E5%9F%BA%E5%9B%9B%E6%B0%9F%E8%8B%AF%E7%B1%BB%E5%8C%96%E5%90%88%E7%89%A9%E4%B8%80%E8%88%AC%E5%85%B7%E6%9C%89%E6%98%93%E7%81%AB%E3%80%81%E6%98%93%E7%86%A0%E7%89%B9%E6%80%A7%EF%BC%8C%E5%9C%A8%E5%82%A8%E5%AD%98%E5%92%8C%E8%BF%90%E8%BE%93%E8%BF%87%E7%A8%8B%E4%B8%AD%E5%BF%85%E9%A1%BB%E4%B8%93%E4%B8%9A%E5%B7%A5%E4%BA%BA%E5%91%98%E6%8C%87%E5%AF%BC%EF%BC%8C%E4%B8%94%E5%BF%85%E9%A1%BB%E4%BF%9D%E8%B4%A3%E3%80%82
Where it is hidden, it is dry and dry, and it is well connected. It is difficult to prevent direct sunlight from burning. The room should not exceed 30 ° C, and the phase should not exceed 80%. Oxidation and edible chemicals should be stored in equal parts, and mixing should not be avoided. There are suitable materials to contain leaks.
For the first time, it is best to use it in the morning and evening. The tank (tank) used in the tank should have a grounding barrier, and the tank can be baffled with holes to generate less shock. It is forbidden to mix oxidation and edible chemicals. On the way, it is necessary to prevent exposure, rain, and high temperature. Halfway through the fire, source, and high temperature. The exhaust pipes of the goods must be equipped with a fire resistor, and it is forbidden to use the equipment and tools that are easy to start fireworks to unload. Highway roads should be driven according to the designated road, and do not stop in residential areas and densely populated areas. Roads should be prohibited from slipping.