2 Ethoxycarbonylamino 5 4 Fluorobenzylamino Nitrobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-ethoxycarbonylamino-5-(4-fluorobenzylamino)nitrobenzene
Chemical Formula C16H16FN3O4
Molecular Weight 333.315 g/mol
Appearance Typically a solid (physical state may vary based on synthesis and purification)
Melting Point Data might vary depending on purity, needs experimental determination
Boiling Point Estimated to be high due to its structure, exact value requires experimental measurement
Solubility Likely sparingly soluble in water, solubility in organic solvents like dichloromethane or ethanol needs testing
Density Value dependent on crystal packing and physical state, requires experimental determination
Pka Relevant acidic or basic groups' pKa values need to be determined through titration methods
Refractive Index Specific to its physical form, determined experimentally
Stability Stability can be affected by light, heat, and air; requires study
Chemical Formula C16H16FN3O4
Molar Mass 333.31 g/mol
Appearance Solid (usually)
Solubility In Water Low (organic compound, likely hydrophobic)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone
Uv Vis Absorption Absorption bands related to aromatic and nitro groups, wavelength depends on solvent
FAQ

What is the chemical structure of 2-ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene?

Alas! To understand the chemical structure of "2 - ethoxycarbonylamino - 5 - (4 - fluorobenzylamino) nitrobenzene", it is necessary to analyze the meaning of its name in detail.

In this name, "benzene" is the name of the benzene ring. It is a six-membered cyclic hydrocarbon with unique stability and chemical properties. "Nitro -" clearly indicates that there is a nitro group (-NO ²) connected to the benzene ring. The introduction of nitro groups changes the electron cloud density of the benzene ring, resulting in changes in its chemical activity.

"2 - ethoxycarbonylamino -" table is connected with ethoxycarbonylamino (- NHCOOCH ³ CH 😉) at the No. 2 position of the benzene ring. This group contains amide bonds (- CONH -) and ethoxy groups (- OCH -2 CH 😉). The amide bond has certain stability, and the ethoxy group affects the lipophilic properties of the molecule.

"5- (4 - fluorobenzylamino) -" means that the No. 5 position of the benzene ring is connected with 4 - fluorobenzyl amino groups (- NHCH -2 C H F), in which the counterposition of the benzyl group (- CH -2 C H) has a fluorine atom (- F) substitution. Fluorine atoms have strong electronegativity, which can affect the electron cloud distribution and polarity of molecules.

In summary, this compound has a benzene ring as the parent nucleus, ethoxycarbonylamino at position 2, 4-fluorobenzyl amino at position 5, and nitro on the benzene ring. The various parts of its structure interact with each other to determine the chemical and physical properties of this compound.

What is the main use of 2-ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene?

2-Ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene is an organic compound. It has a wide range of uses and is often used as a key intermediate in the synthesis of specific drugs in the field of medicinal chemistry. Because the structure contains specific functional groups, it can be chemically transformed to construct molecular structures with specific biological activities, and then provide the possibility for the development of drugs for the treatment of diseases such as inflammation and tumors.

In the field of materials science, or can be used to prepare materials with special properties. Its molecular structure endows materials with unique electrical, optical or mechanical properties, which can be applied to organic optoelectronic materials, polymer composites and other fields, laying the foundation for the development of new functional materials.

Furthermore, in organic synthetic chemistry, it can serve as an important building block, through various organic reactions, interact with other compounds, expand the complexity of molecular structure, synthesize organic compounds with novel structures and specific functions, and contribute to the development and innovation of organic synthesis methodologies.

In short, although 2-ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene is an organic compound, it has important potential uses in many fields such as drugs, materials and organic synthesis due to its unique structure, which is of great significance for promoting the progress of related scientific fields.

2-ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene

The synthesis of 2-ethoxycarbonyl amino-5- (4-fluorobenzyl amino) nitrobenzene is an important topic in the field of organic synthesis. To synthesize this compound, the following steps can be followed.

First, a suitable nitrobenzoic acid derivative is used as the starting material. In this raw material, the localization of the nitro group has a great influence on the subsequent reaction. It is first reacted with ethoxyformyl chloride in an alkaline environment, which is created by organic bases such as pyridine or triethylamine. During the reaction, the carbonyl group of ethoxyformyl chloride undergoes nucleophilic substitution with the amino group in the raw material to generate 2-ethoxycarbonyl amino nitrobenzoic acid derivatives. This step requires attention to the control of the proportion of reactants, reaction temperature and time. The temperature is usually controlled between 0-25 ° C and the duration is about several hours to ensure that the reaction is sufficient and there are few side reactions.

React the above product with 4-fluorobenzyl amine. This step should be carried out in a polar solvent, such as N, N-dimethylformamide (DMF). To promote the reaction, an appropriate amount of base, such as potassium carbonate, can be added. The amino group of 4-fluorobenzyl amine undergoes nucleophilic substitution for the ortho-position of the carboxyl group in the derivative of 2-ethoxycarbonyl amino-nitrobenzoic acid, and the target product 2-ethoxycarbonylamino-5- (4-fluorobenzyl amino) nitrobenzene is formed by condensation reaction. The reaction temperature may be slightly higher, about 60-100 ° C, and the reaction time may vary from a few hours to more than ten hours. During this period, the reaction process needs to be monitored by thin-layer chromatography (TLC).

There may be other methods. Nitrobenzene can be nitrified first, and nitro can be introduced precisely, and then ethoxycarbonylamino and 4-fluorobenzyl amino can be introduced in turn. However, this path requires fine control of the reaction conditions. Due to the slight difference in the order and conditions of the multi-step reaction, it is easy to increase the number of by-products and reduce the yield.

During the synthesis process, the reaction products at each step need to be purified, often by column chromatography or recrystallization. Column chromatography is separated according to the difference in the distribution coefficients of the product and the impurities in the stationary and mobile phases; recrystallization is achieved by the different solubility of the product and the impurity at different temperatures. In this way, after multi-step reaction and purification, the target product 2-ethoxycarbonylamino-5 - (4-fluorobenzylamino) nitrobenzene can be obtained.

What are the physical properties of 2-ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene

2-Ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene is a kind of organic compound. Its physical properties are quite important, and it is related to the performance of this substance in different scenes.

When it comes to appearance, it is usually solid, but the exact color state may vary depending on the purity and conditions of preparation. Generally speaking, it may be a powdery solid like white to light yellow. This appearance characteristic is crucial for identifying and preliminarily judging its quality.

Its melting point is also an important physical property. The melting point is also the critical temperature at which the substance changes from solid to liquid. The melting point of 2-ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene has been determined by many experiments to be in a specific temperature range. This temperature range is an indispensable parameter for the identification of the substance and the control of its production process. Due to the deviation of the melting point, it may suggest a change in the purity of the substance, or the mixing of impurities during the synthesis process.

Solubility cannot be ignored. In common organic solvents, this compound exhibits specific solubility. For example, in some polar organic solvents, it may have a certain solubility, while in non-polar solvents, the solubility may be very small. This difference in solubility provides an important basis for its separation, purification and application in different reaction systems. For example, in an organic synthesis reaction, a suitable solvent is selected to ensure the smooth progress of the reaction, and the solubility of the substance is a key consideration in the selection of the solvent.

Furthermore, density is also one of its physical properties. Although its density data may be little known to the general public, in certain industrial applications and scientific research fields, this parameter is related to the measurement, transportation, and behavior of the substance when mixed with other substances. Knowing its density can accurately calculate the amount of the required substance and avoid deviations in experiments or production due to improper dosage.

The physical properties, appearance, melting point, solubility and density of this 2-ethoxycarbonylamino-5- (4-fluorobenzyl amino) nitrobenzene play a decisive role in its application in many fields such as organic synthesis and drug development. In practical operation, accurate grasp of these properties can make good use of this compound and achieve the desired goal.

2-ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene market prospects

Nowadays, the name of the compound is 2-ethoxycarbonylamino-5- (4-fluorobenzylamino) nitrobenzene. To know its market prospects, I will imitate the text of "Tiangong" and describe it to you.

This compound has the potential to be developed in the field of chemical engineering and materials. In the field of research and development of materials, it may be able to combine the properties of biological macromolecules, which may control physiological activities. If good research is done, it may provide a cornerstone for new generation.

As far as the material field is concerned, its special molecular properties may make the material appear novel. If it is used in light-absorbing materials, it may be possible to give the material special light absorption and light-absorbing properties, and it can be used in new display technologies.

However, the road ahead in the market is not smooth. The degree of research cannot be ignored. In order to precisely control its properties, it is necessary to explore a lot of profound technologies. And the market is intense, other similar compounds may have entered the market first.

However, if it can overcome the problems of research and explore new applications with its characteristics, the market prospect may be bright. In short, this compound is like pure jade, and it will become a great tool for those who are good at it. If it is grasped and well added, it may be able to gain a place in the market.