4 Fluorobenzene 1 3 Diamine
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
4-fluorobenzene-1,3-diamine
Chemical Formula C6H7FN2
Molar Mass 126.13 g/mol
Appearance Solid (usually white or off - white powder)
Odor Typical amine - like odor
Melting Point 102 - 104 °C
Boiling Point 292 - 294 °C
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in polar organic solvents like ethanol, acetone
Flash Point High (above 100 °C, likely around 140 - 150 °C)
Pka For the amine groups, pKa values are in the range of 8 - 10
Chemical Formula C6H7FN2
Molar Mass 126.13 g/mol
Appearance Solid
Color White to off - white
Melting Point 106 - 109 °C
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
Odor Aminic odor
Pka pKa1 ~ 3.95 (for the first amino group protonation), pKa2 ~ 9.95 (for the second amino group protonation)
Density 1.27 g/cm³ (estimated)
Chemical Formula C6H7FN2
Molecular Weight 126.13
Appearance Solid
Color Typically white to off - white
Odor Characteristic amine - like odor
Melting Point 115 - 118 °C
Boiling Point 290 - 295 °C
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
Flash Point 157 °C
Density 1.258 g/cm³ (approximate)
Pka Around 9 - 10 (for amino groups)
FAQ

What are the main uses of 4-fluorobenzene-1,3-diamine?

4-Fluorobenzene-1,3-diamine is a class of organic compounds. It has a wide range of uses and has important applications in many fields.

First, in the field of medicinal chemistry, this compound is often a key intermediate. As far as the development of new drugs is concerned, due to its unique chemical structure, specific functional groups can be introduced to help adjust the activity, selectivity and bioavailability of drug molecules. For example, for some specific disease targets, by modifying and modifying the structure of 4-fluorobenzene-1,3-diamine, drugs with higher efficacy and lower side effects can be synthesized.

Second, in the field of materials science, it also has unique value. In the preparation of high-performance polymer materials, it can participate in the polymerization reaction as a monomer. The resulting polymer materials may have excellent thermal stability, mechanical properties and electrical properties. For example, packaging materials used in the manufacture of electronic devices can improve the insulation and stability of materials and ensure the stable operation of electronic devices.

Third, in the field of dye chemistry, 4-fluorobenzene-1,3-diamine can be used as a raw material for synthesizing new dyes. Because of its fluorine atom and amino group, dyes have unique color characteristics and dyeing properties. The dyes produced may have higher light resistance and washable properties, and can be used in textile, printing and dyeing and other industries to improve dyeing quality.

Furthermore, in the field of pesticide chemistry, based on this, chemically modified pesticides can be synthesized with high insecticidal, bactericidal or herbicidal activities. Its special structure can enhance the interaction with biological targets, improve the activity and selectivity of pesticides, and reduce the impact on the environment.

From the above, 4-fluorobenzene-1,3-diamine plays an important role in the fields of medicine, materials, dyes, pesticides, etc., providing a key chemical basis for the development of various fields.

What are the physical properties of 4-fluorobenzene-1,3-diamine?

4-Fluorobenzene-1,3-diamine is one of the organic compounds. Its physical properties are quite important and are related to many chemical applications.

Looking at its properties, it is mostly white to light yellow crystalline powder under normal conditions. This morphology is easy to observe and identify, and also affects its dispersion and reaction characteristics in different media.

When it comes to the melting point, it is about 108-112 ° C. The melting point is an inherent property of the substance, and the exact melting point value is of great significance for the identification of its purity. If the purity is high, the melting point range is narrow and approaches the theoretical value; if the purity is low, the melting point decreases and the range widens. This melting point value implies that the transition from solid to liquid will occur in the corresponding temperature range. In chemical production and experimental operations, appropriate temperature conditions can be set accordingly to achieve specific reactions or separation processes.

Furthermore, its solubility also has characteristics. The degree of solubility in water is limited, but it exhibits good solubility in common organic solvents such as ethanol and dichloromethane. This solubility characteristic makes it easy to select a suitable solvent system in organic synthesis reactions, ensuring that the reactants are fully contacted and promoting the smooth progress of the reaction. For example, in the reaction system using ethanol as the solvent, 4-fluorobenzene-1,3-diamine can be uniformly dispersed and fully mixed with other reactants to improve the reaction efficiency and product yield.

In addition, the density of the substance is about 1.33 g/cm ³. The physical quantity of density is of great significance in the measurement, transportation and storage of substances. Knowing the density can accurately calculate the mass of a certain volume of the substance, which is convenient for the accurate ratio of raw materials in production. When storing and transporting, consider the choice of packaging and carrying equipment according to the density to ensure safety and convenience.

The physical properties of 4-fluorobenzene-1,3-diamine are interrelated and play a key role in chemical synthesis, materials science and other fields. Only by in-depth understanding and accurate grasp can it be better applied to actual production and scientific research.

What are the chemical properties of 4-fluorobenzene-1,3-diamine?

4-Fluorobenzene-1,3-diamine is a genus of organic compounds. In its molecular structure, above the benzene ring, the fluorine atom occupies the 4th position, and the amino group is in the 1st and 3rd positions. This compound has special chemical properties and is widely used in the field of organic synthesis.

In terms of its physical properties, under normal conditions, it may be a solid, white and powdery. The melting point and boiling point have their own specific values due to the force between molecules. Because it contains amino groups, it can form hydrogen bonds with water, so it has a certain solubility in water. However, due to the non-polarity of the benzene ring, the solubility is also limited.

Its chemical properties are active, and the amino group is alkaline, which can react with acids to form corresponding salts. In case of electrophilic reagents, electrophilic substitution reactions are prone to occur on the benzene ring. Although fluorine atoms have electron-absorbing induction effects, they have their own unique effects on reactivity due to their positional relationships. Amino groups can also participate in many organic reactions, such as reacting with acid chlorides to form amide compounds, which are commonly used in the construction of complex organic molecular structures.

In organic synthesis, 4-fluorobenzene-1,3-diamine is often a key raw material. It can be reacted in multiple steps to prepare various drug intermediates and functional materials. Because of its unique structure and properties, it can endow the products with special functions and properties, so it has attracted much attention in the chemical, pharmaceutical and other industries.

What are the synthesis methods of 4-fluorobenzene-1,3-diamine?

4-Fluorobenzene-1,3-diamine is also an organic compound. The synthesis method is quite complicated and is described in detail.

One method can be obtained by reducing 4-fluoro-1,3-dinitrobenzene. First take 4-fluoro-1,3-dinitrobenzene, place it in a suitable reactor, add an appropriate amount of solvent, such as ethanol, methanol, etc., to help dissolve. Next, add a reducing agent, such as a combination of iron powder and hydrochloric acid. Iron powder needs to be finely ground to increase the reaction area and accelerate the reaction process. Heat slowly and maintain a certain temperature, about 60-80 degrees Celsius. During the reaction, stirring is required to make the reactants fully contact. After several times of reaction, the nitro group of 4-fluoro-1,3-dinitrobenzene is gradually reduced to an amino group, and then 4-fluorobenzene-1,3-diamine is obtained. After the reaction is completed, the reaction solution is cooled, and the product is separated by appropriate methods, such as filtration, distillation, etc., and then purified to obtain pure 4-fluorobenzene-1,3-diamine.

Another method can be started from 4-fluoroaniline. First, 4-fluoroaniline is substituted with appropriate reagents to introduce nitro groups to obtain 4-fluoro-3-nitroaniline. In this process, reagents and reaction conditions need to be carefully selected to ensure that the position of nitro introduction is accurate. Then the nitro group of 4-fluoro-3-nitroaniline is reduced to an amino group. The reduction step is similar to the previous method. Iron powder-hydrochloric acid can be used, and catalytic hydrogenation can also be used. When catalyzing hydrogenation, a suitable catalyst, such as palladium carbon, should be selected to react at a certain pressure and temperature. After this two-step reaction, 4-fluorobenzene-1,3-diamine can also be obtained. The product also needs to be separated and purified to achieve the required purity.

The method of synthesizing 4-fluorobenzene-1,3-diamine has its own advantages and disadvantages. In practical application, the appropriate method should be carefully selected according to specific needs, availability of raw materials and costs.

What is the price range of 4-fluorobenzene-1,3-diamine in the market?

I think what you are asking is that 4-fluorobenzene-1,3-diamine is within the market price range. However, the price of this chemical substance is affected by various factors, and it is difficult to determine with certainty.

First, the price of raw materials is also dynamic. If the price of raw materials required for the production of 4-fluorobenzene-1,3-diamine changes over time, or rises and falls due to origin, supply and demand, the price of finished products will also change. If the output of raw materials decreases sharply, causing the price of raw materials to rise, the price of this compound will also rise.

Second, the difficulty of preparation is related to cost, and it also affects its price. If the preparation method is difficult, multiple processes are required, or expensive instruments and reagents are used, the cost is high, and the price is not low. If there is a new and simple method, the cost will drop, and the price may fall.

Third, the market supply and demand is the main reason. If there are many people who want this compound, but the production is insufficient, the price will tend to be higher; if there are many products and few users, the supply will exceed the demand, and the price will tend to be lower.

Fourth, the manufacturer's brand and purity specifications are also affected. Produced by famous factories, or due to good quality and reputation, the price is slightly higher; those with high purity are also higher than those with low purity.

In summary, in the market, the price of 4-fluorobenzene-1,3-diamine, or due to the above reasons, varies from a few yuan to tens of yuan per gram, but it is difficult to give an accurate price range. It must be studied carefully according to the current market conditions.