1 4 Fluorobenzyl Piperazinediium
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
1-(4-fluorobenzyl)piperazinediium
Name 1-(4-fluorobenzyl)piperazinediium
Chemical Formula C11H16F N2+
Molar Mass 194.26 g/mol
Appearance Solid (predicted)
Solubility In Water Unknown
Solubility In Organic Solvents Unknown
Pka Unknown
Logp Unknown
Density Unknown
Chemical Formula C11H16F2N2
Molecular Weight 214.255 g/mol
FAQ

What is the chemical structure of 1- (4-fluorobenzyl) piperazinediium?

The chemical structure of 1 - (4 - fluorobenzyl) piperazine diammonium has a unique structure. The piperazine ring is the core structure of this compound, which is like a cyclic foundation, stable and critical. On the piperazine ring, there is a (4 - fluorobenzyl) group at 1 position. In this group, the benzyl group is a phenyl-linked methylene structure, and the 4-position of the benzene ring is complex with fluorine atoms. The introduction of fluorine atoms has a high electronegativity, which has a great impact on the electron cloud distribution and chemical properties of the whole molecule. Furthermore, the term "diammonium" indicates that the molecule has two ammonium ion parts. Ammonium ions are formed by combining nitrogen atoms with four hydrogen atoms and are positively charged. The existence of this positive charge makes the compound exhibit unique characteristics in chemical reactions and interactions with other substances. Overall, the chemical structure of 1 - (4-fluorobenzyl) piperazine diammonium is composed of piperazine ring, (4-fluorobenzyl) group and ammonium ion parts. The parts interact and cooperate with each other, giving this compound specific physical and chemical properties, and may have unique uses and performances in many chemical and related fields.

What are the main uses of 1- (4-fluorobenzyl) piperazinediium?

1 - (4 - fluorobenzyl) piperazine diammonium, this is an organic compound. It has a wide range of uses and has important applications in many fields.

In the field of medicinal chemistry, it is often used as a key intermediate. Due to its unique chemical structure, it can participate in various reactions and assist in the synthesis of drug molecules with specific biological activities. For example, some piperazine derivatives with specific pharmacological effects, 1 - (4 - fluorobenzyl) piperazine diammonium may be an important starting material. After a series of chemical transformations, drugs with therapeutic effects on specific diseases such as neurological diseases and cardiovascular diseases can be prepared.

In the field of materials science, it also has good performance. Can be used to prepare special functional materials. Such as participating in the synthesis of polymer materials, endowing materials with unique properties such as good solubility, thermal stability or special optical and electrical properties. These special materials may have important applications in electronic devices, optical instruments, etc., such as insulating materials for manufacturing high-performance electronic components, or display materials with special optical properties.

In the field of organic synthetic chemistry, 1 - (4-fluorobenzyl) piperazine diammonium is an extremely useful reagent. Due to the presence of piperazine ring and fluorobenzyl group in its structure, it can introduce unique activity check points and spatial structures for reactions, promote the construction of various complex organic molecules, help chemists achieve novel and challenging synthesis goals, and provide important support for the development of organic synthetic chemistry.

What are the physical properties of 1- (4-fluorobenzyl) piperazinediium?

1 - (4-fluorobenzyl) piperazine diazonium, its physical properties are of high value for investigation. The outer surface of this substance is often in a specific shape, or it is crystalline, the crystal shape is complete, and it has a certain luminosity. Its color may vary depending on the degree of color, but it is mostly transparent or light-colored. In terms of solubility, it exhibits different properties in a specific solution. In water, it is often soluble. This substance may be slightly soluble in water. When it is dissolved, water molecules interact with their molecules, resulting in a slow dissolution rate and limited dissolution. However, with dissolution, such as ethanol and acetone, its solubility may be improved. Due to the fit of the molecular forces of the dissolution, it can be well dispersed and the solubility phase increases.

The melting temperature is also an important physical property. The melting temperature is defined to a certain extent, and the external temperature is determined by this specific value. The solid 1 - (4-fluorobenzyl) piperazine diazonium is the melting liquid. This process absorbs, the molecular distance is large, and the lattice disintegrates. The boiling temperature is higher, and more energy needs to be provided to make the liquid molecules interact with each other and escape the liquid surface.

In terms of density, the phase density or some constants can be determined by the phase method. This property affects its distribution in the mixture. In addition, the refractive index of this substance also has a specific value. The degree of refraction depends on the molecular temperature and the arrangement of its molecules. This property can be used for determination and analysis. Therefore, the physical properties of 1- (4-fluorobenzyl) piperazine diazonium determine the density of its molecules, and its application in many fields is of great importance.

What is the preparation method of 1- (4-fluorobenzyl) piperazinediium?

The preparation method of 1 - (4 -fluorobenzyl) piperazine diammonium is as follows:
First take an appropriate amount of 4-fluorobenzyl halide, usually 4-fluorobenzyl chloride or 4-fluorobenzyl bromide. Place it in a suitable reaction vessel, which needs to be clean and dry to prevent impurities from interfering with the reaction.
Take another piperazine. According to a certain stoichiometric ratio, the molar ratio of piperazine to 4-fluorobenzyl halide is usually controlled within a certain range, about 1.0-1.2:1. Add piperazine slowly to the reaction vessel containing 4-fluorobenzyl halide. This process should be carried out under gentle stirring to make full contact between the two.
The reaction system needs to be controlled at a suitable temperature, generally between 50 and 80 ° C. It can be precisely controlled by heating in an oil or water bath. Maintain this temperature and continue to stir the reaction for several hours, about 3 to 6 hours. Pay close attention to system changes during the reaction process.
After the reaction is completed, the reaction mixture is cooled to room temperature. Then, an appropriate amount of organic solvent, such as ether or ethyl acetate, is added to extract the product. Extract several times to ensure that the product is fully transferred to the organic phase.
Combine the organic phases and dry them with anhydrous sodium sulfate or magnesium sulfate to remove the residual moisture. After filtering to remove the desiccant, distill under reduced pressure to remove the organic solvent to obtain a crude product.
The crude product can be further purified by column chromatography or recrystallization. During column chromatography, choose a suitable eluent, such as a solution of petroleum ether and ethyl acetate mixed in a certain proportion. For recrystallization, choose a suitable solvent, such as ethanol or acetone. After multiple crystallization operations, high purity 1 - (4 -fluorobenzyl) piperazine diammonium can be obtained.

What are the precautions for using 1- (4-fluorobenzyl) piperazinediium?

1 - (4-fluorobenzyl) piperazinobium is a chemical compound. During the course of use, please pay attention to the general situation.

First, it is very important to be safe. This compound may be toxic and irritating to a certain extent, and direct contact must be avoided. For operation, it is advisable to wear protective clothing, such as gloves, eyes, clothing, etc., to prevent skin and eyes from being invaded. If it is accidentally connected, it should be washed with a large amount of water immediately, and it is necessary to seek treatment.

Furthermore, its chemical properties also need to be considered. 1 - (4-fluorobenzyl) piperazinobium or polymers should be avoided for storage and use. Incompatible substances should be avoided. Before use, it is necessary to understand its chemical characteristics, and control the anti-friction parts according to the requirements of the anti-friction, such as degree, force, anti-friction, etc., in order to ensure the anti-friction and avoid accidental occurrence.

In terms of storage, it is also not allowed to be small. It should be placed in a well-preserved, dry, and well-connected environment, and the source of ignition and pollution. Depending on the characteristics of the compound, specific storage parts may be required, such as protection from light, sealing, etc., to maintain their characterization and prevent damage.

In addition, the raw materials in the use process also need to be properly handled. Do not lose your mind, follow the relevant protection law, collect them separately, and hand them over to the warehouse for treatment to prevent pollution.

Therefore, the use of 1- (4-fluorobenzyl) piperazine diazonium requires attention to various aspects such as safety, chemical properties, storage, and physical management, so as to ensure the safety and effectiveness of the operation.