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1-(4-Chloro-1-Phenylbutyl)-4-Fluorobenzene
Linshang Chemical
|
HS Code |
385135 |
| Chemical Formula | C16H16ClF |
| Molecular Weight | 264.75 |
As an accredited 1-(4-Chloro-1-Phenylbutyl)-4-Fluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1-(4 - chloro - 1 - phenylbutyl)-4 - fluorobenzene in a sealed chemical - grade container. |
| Storage | 1-(4 - chloro - 1 - phenylbutyl)-4 - fluorobenzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly - sealed container, preferably made of corrosion - resistant material, to prevent leakage and contamination. Label the storage container clearly with its name, hazards, and handling instructions. |
| Shipping | 1-(4 - chloro - 1 - phenylbutyl)-4 - fluorobenzene is shipped in properly sealed, corrosion - resistant containers. Special handling per chemical regulations is ensured to prevent spills and maintain safety during transit. |
Competitive 1-(4-Chloro-1-Phenylbutyl)-4-Fluorobenzene prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 1-(4-Chloro-1-Phenylbutyl)-4-Fluorobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the main uses of 1- (4-chloro-1-phenylbutyl) -4-fluorobenzene?
The main uses of 1- (4-mercury-1-benzylacetyl) -4-bromobenzyl are related to many fields. This compound is often used as a key intermediate in the field of medicinal chemistry. In organic synthesis, its structural properties can be converted into substances with specific biological activities through clever chemical reactions, or used to create new drugs to treat various diseases.
In the field of materials science, 1- (4-mercury-1-benzylacetyl) -4-bromobenzyl also has its uses. Through the polymerization reaction or modification process in which it participates, materials with specific properties can be prepared, such as those with unique electrical, optical or mechanical properties, to meet the needs of electronic devices, optical materials and other industries.
Furthermore, in the fine chemical industry, the compound can be used to synthesize high value-added fine chemicals. Due to its unique structure, a series of fine chemical products can be derived, which are widely used in the production of fragrances, dyes, additives, etc., contributing to the improvement of product quality and performance.
In summary, 1 - (4 - mercury - 1 - benzylacetyl) - 4 - bromobenzyl, with its unique structure, plays an important role in many fields such as medicine, materials, and fine chemicals, and is of great significance to promote the development of related industries.
In the field of materials science, 1- (4-mercury-1-benzylacetyl) -4-bromobenzyl also has its uses. Through the polymerization reaction or modification process in which it participates, materials with specific properties can be prepared, such as those with unique electrical, optical or mechanical properties, to meet the needs of electronic devices, optical materials and other industries.
Furthermore, in the fine chemical industry, the compound can be used to synthesize high value-added fine chemicals. Due to its unique structure, a series of fine chemical products can be derived, which are widely used in the production of fragrances, dyes, additives, etc., contributing to the improvement of product quality and performance.
In summary, 1 - (4 - mercury - 1 - benzylacetyl) - 4 - bromobenzyl, with its unique structure, plays an important role in many fields such as medicine, materials, and fine chemicals, and is of great significance to promote the development of related industries.
What are the physical properties of 1- (4-chloro-1-phenylbutyl) -4-fluorobenzene?
4-Cyanogen-1-naphthyl-methyl-4-cyanonaphthalene, this is an organic compound. Its physical properties are as follows:
Appearance morphology, often white to light yellow crystalline powder, this morphology is more common in many organic compounds, easy to observe and process.
Melting point is about 160-165 ℃. As a key physical property of a substance, the melting point plays a decisive role in its phase transition under specific conditions. Knowing the melting point helps to accurately control the temperature conditions when synthesizing, purifying and applying the substance.
Solubility, difficult to dissolve in water. This is mainly due to the hydrophobicity of the cyano and naphthalene groups in its molecular structure, which makes it difficult to form effective interactions with water molecules. However, it is soluble in common organic solvents, such as dichloromethane, chloroform, N, N-dimethylformamide (DMF), etc. This solubility characteristic provides convenience for its application in organic synthesis reactions, and can select suitable organic solvents as reaction media according to the needs of the reaction to promote the smooth progress of the reaction.
In terms of stability, it has certain stability under conventional conditions, but it needs to avoid contact with strong oxidants, strong acids, strong bases and other substances. Due to the relatively active chemical properties of the cyanyl group in the molecule, reactions such as hydrolysis and addition may occur under specific chemical environments, which may affect the structure and properties of the substance. During storage and use, it is necessary to pay attention to its chemical compatibility to prevent accidental chemical reactions and ensure its stability and safety.
Appearance morphology, often white to light yellow crystalline powder, this morphology is more common in many organic compounds, easy to observe and process.
Melting point is about 160-165 ℃. As a key physical property of a substance, the melting point plays a decisive role in its phase transition under specific conditions. Knowing the melting point helps to accurately control the temperature conditions when synthesizing, purifying and applying the substance.
Solubility, difficult to dissolve in water. This is mainly due to the hydrophobicity of the cyano and naphthalene groups in its molecular structure, which makes it difficult to form effective interactions with water molecules. However, it is soluble in common organic solvents, such as dichloromethane, chloroform, N, N-dimethylformamide (DMF), etc. This solubility characteristic provides convenience for its application in organic synthesis reactions, and can select suitable organic solvents as reaction media according to the needs of the reaction to promote the smooth progress of the reaction.
In terms of stability, it has certain stability under conventional conditions, but it needs to avoid contact with strong oxidants, strong acids, strong bases and other substances. Due to the relatively active chemical properties of the cyanyl group in the molecule, reactions such as hydrolysis and addition may occur under specific chemical environments, which may affect the structure and properties of the substance. During storage and use, it is necessary to pay attention to its chemical compatibility to prevent accidental chemical reactions and ensure its stability and safety.
What are the chemical properties of 1- (4-chloro-1-phenylbutyl) -4-fluorobenzene?
The chemical properties of 1- (4-neon-1-silylethylsilyl) -4-deuterium silicon are key to the properties of substances in chemical reactions. This compound has unique chemical properties because it contains elements such as neon and silicon.
Neon is a rare gas with stable chemical properties and often exists in nature in elemental form. In this compound, although the chemical activity of neon is limited, its existence can affect the molecular structure and electron cloud distribution, which in turn affects the overall properties.
Silicon, as an important component of semiconductor materials, has a valence electron structure that allows it to form a variety of chemical bonds. In 1- (4-neon-1-silyethylsilyl) -4-deuterium silicon, silicon atoms are connected to surrounding atoms by covalent bonds to build complex molecular structures. The properties of silicon-silicon bonds and silicon-other atomic bonds determine the stability and reactivity of the compound.
Deuterium, as an isotope of hydrogen, has a slightly larger mass than hydrogen. In compounds, deuterium substitution can change the vibrational frequency of chemical bonds, affecting molecular dynamics and chemical reaction rates. Due to the difference in the strength of deuterium-silicon bonds and hydrogen-silicon bonds, 1- (4-neon-1-silylethylsilyl) - 4-deuterium-silicon may behave differently from hydrogen-containing analogues in reactions involving the breaking and formation of chemical bonds.
This compound may have certain thermal stability. In view of the strength of silicon-silicon bonds and silicon-other atomic bonds, its structure may remain stable over a moderate temperature range. In case of high temperature, chemical bonds may break or rearrange, leading to chemical reactions and the formation of new products. In terms of chemical activity, the compound may react with electrophilic reagents and nucleophilic reagents because the outer electrons of silicon atoms can participate in the reaction. The specific reactivity depends on the electron cloud density distribution of each atom in the molecule and the steric hindrance. Where the steric hindrance is large, the reaction reagent is close to or hindered by the reaction; while in areas with high electron cloud density, it is easy to attract electrophilic reagents and initiate reactions.
Neon is a rare gas with stable chemical properties and often exists in nature in elemental form. In this compound, although the chemical activity of neon is limited, its existence can affect the molecular structure and electron cloud distribution, which in turn affects the overall properties.
Silicon, as an important component of semiconductor materials, has a valence electron structure that allows it to form a variety of chemical bonds. In 1- (4-neon-1-silyethylsilyl) -4-deuterium silicon, silicon atoms are connected to surrounding atoms by covalent bonds to build complex molecular structures. The properties of silicon-silicon bonds and silicon-other atomic bonds determine the stability and reactivity of the compound.
Deuterium, as an isotope of hydrogen, has a slightly larger mass than hydrogen. In compounds, deuterium substitution can change the vibrational frequency of chemical bonds, affecting molecular dynamics and chemical reaction rates. Due to the difference in the strength of deuterium-silicon bonds and hydrogen-silicon bonds, 1- (4-neon-1-silylethylsilyl) - 4-deuterium-silicon may behave differently from hydrogen-containing analogues in reactions involving the breaking and formation of chemical bonds.
This compound may have certain thermal stability. In view of the strength of silicon-silicon bonds and silicon-other atomic bonds, its structure may remain stable over a moderate temperature range. In case of high temperature, chemical bonds may break or rearrange, leading to chemical reactions and the formation of new products. In terms of chemical activity, the compound may react with electrophilic reagents and nucleophilic reagents because the outer electrons of silicon atoms can participate in the reaction. The specific reactivity depends on the electron cloud density distribution of each atom in the molecule and the steric hindrance. Where the steric hindrance is large, the reaction reagent is close to or hindered by the reaction; while in areas with high electron cloud density, it is easy to attract electrophilic reagents and initiate reactions.
What are the synthesis methods of 1- (4-chloro-1-phenylbutyl) -4-fluorobenzene?
To prepare 1 - (4 - cyano- 1 - naphthyl) - 4 - cyanonaphthalene, the synthesis method is as follows:
can be started from a suitable naphthalene derivative, through a halogenation reaction, the naphthalene ring is introduced into a specific position of the halogen atom, which is highly active and can be used as an activity check point for subsequent reactions. For example, using naphthalene as a raw material, under appropriate conditions, a halogen reagent such as bromine or chlorine can be used to introduce a bromine atom or a chlorine atom into the naphthalene ring under the action of a catalyst.
Then, the cyanidation reaction is used to replace the introduced halogen atom with a This cyanidation reaction requires the selection of appropriate cyanide reagents, such as potassium cyanide, sodium cyanide, etc., and is carried out under suitable solvents and reaction conditions. In this process, the halogen atom and the cyanide reagent undergo a nucleophilic substitution reaction, the halogen atom leaves, and the cyanide group is connected to form a cyanide-containing naphthalene derivative.
For the construction of the structure of 1- (4-cyano1-naphthalene) -4-cyanonaphthalene, the above-mentioned cyanogroup-containing naphthalene derivatives can be coupled through suitable organic reactions, such as under certain conditions. This coupling reaction requires the selection of a suitable catalyst and reaction system, so that the two naphthalene derivative molecules are connected at a specific position to form a carbon-carbon bond of the target product, and then complete the synthesis of 1- (4-cyano- 1-naphthalene) - 4-cyanonaphthalene.
In addition, the reaction conditions need to be precisely controlled during the reaction process, such as temperature, reaction time, and reactant ratio, to ensure that the reaction proceeds in the direction of generating the target product, while minimizing the occurrence of side reactions and improving the yield and purity of the product. And after each step of the reaction, the product needs to be separated and purified to meet the requirements of the next reaction. Thus, the synthesis of 1 - (4 -cyano-1 -naphthyl) - 4 -cyanonaphthalene can be achieved by carefully designed reaction and treatment in multiple steps.
can be started from a suitable naphthalene derivative, through a halogenation reaction, the naphthalene ring is introduced into a specific position of the halogen atom, which is highly active and can be used as an activity check point for subsequent reactions. For example, using naphthalene as a raw material, under appropriate conditions, a halogen reagent such as bromine or chlorine can be used to introduce a bromine atom or a chlorine atom into the naphthalene ring under the action of a catalyst.
Then, the cyanidation reaction is used to replace the introduced halogen atom with a This cyanidation reaction requires the selection of appropriate cyanide reagents, such as potassium cyanide, sodium cyanide, etc., and is carried out under suitable solvents and reaction conditions. In this process, the halogen atom and the cyanide reagent undergo a nucleophilic substitution reaction, the halogen atom leaves, and the cyanide group is connected to form a cyanide-containing naphthalene derivative.
For the construction of the structure of 1- (4-cyano1-naphthalene) -4-cyanonaphthalene, the above-mentioned cyanogroup-containing naphthalene derivatives can be coupled through suitable organic reactions, such as under certain conditions. This coupling reaction requires the selection of a suitable catalyst and reaction system, so that the two naphthalene derivative molecules are connected at a specific position to form a carbon-carbon bond of the target product, and then complete the synthesis of 1- (4-cyano- 1-naphthalene) - 4-cyanonaphthalene.
In addition, the reaction conditions need to be precisely controlled during the reaction process, such as temperature, reaction time, and reactant ratio, to ensure that the reaction proceeds in the direction of generating the target product, while minimizing the occurrence of side reactions and improving the yield and purity of the product. And after each step of the reaction, the product needs to be separated and purified to meet the requirements of the next reaction. Thus, the synthesis of 1 - (4 -cyano-1 -naphthyl) - 4 -cyanonaphthalene can be achieved by carefully designed reaction and treatment in multiple steps.
What are the precautions for using 1- (4-chloro-1-phenylbutyl) -4-fluorobenzene?
1-%284-%E6%B0%AF-1-%E8%8B%AF%E5%9F%BA%E4%B8%81%E5%9F%BA%29-4-%E6%B0%9F%E8%8B%AF%E7%94%A8%E6%B3%95%E4%B8%AD%E5%BF%85%E9%A1%BB%E6%B3%A8%E6%84%8F%E4%B9%8B%E4%BA%8B%EF%BC%8C%E5%85%88%E8%A7%81%E4%B8%8B%E6%96%B9%E5%8D%95%E7%9B%AE%E5%88%86%E6%9E%90%EF%BC%9A
1. 1-%284-%E6%B0%AF-1-%E8%8B%AF%E5%9F%BA%E4%B8%81%E5%9F%BA%29
- This is the initial step of mixing 1 - (4 - ammonia - 1 - naphthyl) - 4 - sulfonic acid. It is necessary to control the ratio of each raw material, and the quality of the raw material is also very important. If the raw material contains high content, the quality of the easy-to-see material is low. For example, if there are other factors in the 4 - ammonia - 1 - naphthyl group, or the external side effects are introduced into the reaction, so that the composition of the reaction is low, and the temperature and pH value of the reaction environment need to be precisely controlled. High or low pH may cause the reaction rate to be normal, and even cause side reactions. If the pH value is not high, it will also cause the reaction, just like the activity of the reaction.
2.4-%E6%B0%9F%E8%8B%AF
- In the process of synthesizing 4-sulfonaphthalene, the cleanliness of the reaction cannot be ignored. If other chemicals are left behind, the reaction or reaction may be generated and pollute.
- The reaction rate needs to be controlled. The reaction rate is short, the reaction rate is not complete, and the reaction rate is low; the reaction rate is low, and the reaction may cause the decomposition of the reaction or a step-by-step reaction, reducing the reaction rate.
- It is important to improve the step. Can be used in combination of methods, such as crystallization, extraction, chromatography, etc. Different methods of extraction are used for compounds with different characteristics, and different methods are not used to obtain high-quality 4-sulfonate naphthalene. For example, if the solubility of the mixture is large, the crystallization method may be effective for separation; if the solubility of the mixture is clear, the chromatography method may be more suitable.
In addition, 1- (4-ammonia-1-naphthyl) -4-sulfonic acid and 4-sulfonic naphthalene in the course of use, the control of raw materials, anti-corrosion parts, etc., all need to be careful in order to ensure its performance and the use effect during the period of time.
1. 1-%284-%E6%B0%AF-1-%E8%8B%AF%E5%9F%BA%E4%B8%81%E5%9F%BA%29
- This is the initial step of mixing 1 - (4 - ammonia - 1 - naphthyl) - 4 - sulfonic acid. It is necessary to control the ratio of each raw material, and the quality of the raw material is also very important. If the raw material contains high content, the quality of the easy-to-see material is low. For example, if there are other factors in the 4 - ammonia - 1 - naphthyl group, or the external side effects are introduced into the reaction, so that the composition of the reaction is low, and the temperature and pH value of the reaction environment need to be precisely controlled. High or low pH may cause the reaction rate to be normal, and even cause side reactions. If the pH value is not high, it will also cause the reaction, just like the activity of the reaction.
2.4-%E6%B0%9F%E8%8B%AF
- In the process of synthesizing 4-sulfonaphthalene, the cleanliness of the reaction cannot be ignored. If other chemicals are left behind, the reaction or reaction may be generated and pollute.
- The reaction rate needs to be controlled. The reaction rate is short, the reaction rate is not complete, and the reaction rate is low; the reaction rate is low, and the reaction may cause the decomposition of the reaction or a step-by-step reaction, reducing the reaction rate.
- It is important to improve the step. Can be used in combination of methods, such as crystallization, extraction, chromatography, etc. Different methods of extraction are used for compounds with different characteristics, and different methods are not used to obtain high-quality 4-sulfonate naphthalene. For example, if the solubility of the mixture is large, the crystallization method may be effective for separation; if the solubility of the mixture is clear, the chromatography method may be more suitable.
In addition, 1- (4-ammonia-1-naphthyl) -4-sulfonic acid and 4-sulfonic naphthalene in the course of use, the control of raw materials, anti-corrosion parts, etc., all need to be careful in order to ensure its performance and the use effect during the period of time.
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