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1-[3-((2S)Pyrrolidin-2-Yl)Phenoxy]-4-Chlorobenzene
Linshang Chemical
|
HS Code |
818939 |
| Chemical Formula | C16H15ClNO |
| Molecular Weight | 273.75 |
| Physical State | Solid (predicted) |
| Appearance | Off - white to light yellow solid |
| Melting Point | No data found |
| Boiling Point | No data found |
| Solubility | Soluble in organic solvents like DMSO, methanol |
| Density | No data found |
| Pka | No data found |
| Logp | No data found |
As an accredited 1-[3-((2S)Pyrrolidin-2-Yl)Phenoxy]-4-Chlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1 - [3 - ((2s)pyrrolidin - 2 - yl)phenoxy] - 4 - chlorobenzene in sealed chemical - grade containers. |
| Storage | Store 1 - [3 - ((2s)pyrrolidin - 2 - yl)phenoxy]-4 - chlorobenzene in a cool, dry place away from direct sunlight. Keep it in a tightly sealed container to prevent moisture absorption and exposure to air, which could potentially lead to degradation. Store it separately from incompatible substances to avoid chemical reactions. |
| Shipping | The chemical 1 - [3 - ((2s)pyrrolidin - 2 - yl)phenoxy]-4 - chlorobenzene will be shipped in specialized, well - sealed containers. These ensure safe transit, safeguarding against spills and maintaining chemical integrity during transportation. |
Competitive 1-[3-((2S)Pyrrolidin-2-Yl)Phenoxy]-4-Chlorobenzene prices that fit your budget—flexible terms and customized quotes for every order.
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What is the chemical structure of 1- [3- ((2s) pyrrolidin-2-yl) phenoxy] -4-chlorobenzene?
This is the name of the organic compound. In order to deduce its chemical structure according to this name, the meaning of each part needs to be analyzed in detail. "1 - [3- (2s) pyrrolidin - 2 - yl) phenoxy] - 4 - chlorobenzene", "1 -" and "4 -" indicate that the substitution is based on the benzene ring. "4 - chlorobenzene", it can be seen that the 4th position of the benzene ring has a chlorine atom substitution. "[3- ((2s) pyrrolidin - 2 - yl) phenoxy]", this part indicates the existence of a structure linked to a phenoxy group, and the 3rd position of the phenoxy group is connected to (2s) - 2 - pyrrolidinyl. ( 2S) -2 -pyrrolidinyl is a pyrrolidine ring with a specific stereoconfiguration, and its 2 positions are connected to the 3 positions of the phenoxy group. In summary, the chemical structure of this compound is a benzene ring, with a chlorine atom at 4 positions and a phenoxy group containing (2s) -2 -pyrrolidyl at 1 position. In ancient Chinese, this organic compound, according to its name, has its structure. Above the benzene ring, four chlorine atoms are occupied, and one is connected. It is a phenoxy group containing a specific pyrrolidine group. This is the approximation of its chemical structure.
What are the physical properties of 1- [3- ((2s) pyrrolidin-2-yl) phenoxy] -4-chlorobenzene?
1-%5B3-%28%282s%29pyrrolidin-2-yl%29phenoxy%5D-4-chlorobenzene is an organic compound. The physical properties of this compound, let me explain in detail.
Looking at its appearance, under room temperature and pressure, it may appear in a solid state. This is due to the strong intermolecular forces, which make the molecules closely arranged, so it exists in a solid state. Its melting point is an important physical parameter, but I regret that I have not obtained an exact value. In general, the structure of benzene-containing rings and heterocycles has complex intermolecular interactions, or the melting point is relatively high.
As for the boiling point, it is also related to the characteristics of the molecular structure. The presence of benzene rings, pyrrolidinyl groups and chlorine atoms in the molecules of this compound makes the intermolecular forces rich and diverse. Van der Waals forces, dipole-dipole interactions, and possible hydrogen bonding affect its boiling point. It is speculated that its boiling point is also quite high, because more energy is required to make the molecules break free from each other and become gaseous.
In terms of solubility, in view of its organic properties, it may have certain solubility in common organic solvents such as ethanol, ether, dichloromethane, etc. Due to the principle of "similar miscibility", the non-polar part of the compound attracts each other with the non-polar region of the organic solvent, causing dissolution. However, in water, due to the limited polar groups in its structure and the strong overall hydrophobicity, the solubility should not be good.
Density is also one of the physical properties. Its density is related to the molecular weight and the way of molecular packing. The complex structure of this compound may make its density different from that of common simple organic compounds, but the exact value needs to be determined experimentally to be accurate.
The physical properties of this compound are influenced by its unique molecular structure and are of key significance in both chemical research and practical applications.
Looking at its appearance, under room temperature and pressure, it may appear in a solid state. This is due to the strong intermolecular forces, which make the molecules closely arranged, so it exists in a solid state. Its melting point is an important physical parameter, but I regret that I have not obtained an exact value. In general, the structure of benzene-containing rings and heterocycles has complex intermolecular interactions, or the melting point is relatively high.
As for the boiling point, it is also related to the characteristics of the molecular structure. The presence of benzene rings, pyrrolidinyl groups and chlorine atoms in the molecules of this compound makes the intermolecular forces rich and diverse. Van der Waals forces, dipole-dipole interactions, and possible hydrogen bonding affect its boiling point. It is speculated that its boiling point is also quite high, because more energy is required to make the molecules break free from each other and become gaseous.
In terms of solubility, in view of its organic properties, it may have certain solubility in common organic solvents such as ethanol, ether, dichloromethane, etc. Due to the principle of "similar miscibility", the non-polar part of the compound attracts each other with the non-polar region of the organic solvent, causing dissolution. However, in water, due to the limited polar groups in its structure and the strong overall hydrophobicity, the solubility should not be good.
Density is also one of the physical properties. Its density is related to the molecular weight and the way of molecular packing. The complex structure of this compound may make its density different from that of common simple organic compounds, but the exact value needs to be determined experimentally to be accurate.
The physical properties of this compound are influenced by its unique molecular structure and are of key significance in both chemical research and practical applications.
What are the main uses of 1- [3- ((2s) pyrrolidin-2-yl) phenoxy] -4-chlorobenzene?
1-%5B3-%28%282s%29pyrrolidin-2-yl%29phenoxy%5D-4-chlorobenzene, this is the name of an organic compound. It has a wide range of uses and is reflected in many fields.
In the field of medicinal chemistry, such compounds are often used as lead compounds for the development of new drugs. Due to their special chemical structure, they may interact with specific targets in organisms and exhibit unique biological activities, such as potential antibacterial, antiviral or anti-tumor effects. Researchers use this to explore their potential for disease treatment and hope to develop innovative drugs with excellent efficacy and minimal side effects.
In the field of materials science, the compound may have specific electrical, optical or mechanical properties due to its structural properties, which can be used to prepare new functional materials. For example, it can be used as an organic semiconductor material in devices such as organic Light Emitting Diode (OLED) and organic field effect transistor (OFET), injecting new impetus into the progress of materials science.
In pesticide chemistry, its structural characteristics may give it the ability to inhibit or kill certain pests or pathogens, so it can be used as the basis for the development of new high-efficiency and low-toxicity pesticides, helping agricultural production and ensuring crop yield and quality.
In short, 1-%5B3-%28%282s%29pyrrolidin-2-yl%29phenoxy%5D-4-chlorobenzene has broad application prospects and research value in medicine, materials, pesticides and other fields with its unique chemical structure, providing new opportunities and directions for the development of various fields.
In the field of medicinal chemistry, such compounds are often used as lead compounds for the development of new drugs. Due to their special chemical structure, they may interact with specific targets in organisms and exhibit unique biological activities, such as potential antibacterial, antiviral or anti-tumor effects. Researchers use this to explore their potential for disease treatment and hope to develop innovative drugs with excellent efficacy and minimal side effects.
In the field of materials science, the compound may have specific electrical, optical or mechanical properties due to its structural properties, which can be used to prepare new functional materials. For example, it can be used as an organic semiconductor material in devices such as organic Light Emitting Diode (OLED) and organic field effect transistor (OFET), injecting new impetus into the progress of materials science.
In pesticide chemistry, its structural characteristics may give it the ability to inhibit or kill certain pests or pathogens, so it can be used as the basis for the development of new high-efficiency and low-toxicity pesticides, helping agricultural production and ensuring crop yield and quality.
In short, 1-%5B3-%28%282s%29pyrrolidin-2-yl%29phenoxy%5D-4-chlorobenzene has broad application prospects and research value in medicine, materials, pesticides and other fields with its unique chemical structure, providing new opportunities and directions for the development of various fields.
What are the synthesis methods of 1- [3- ((2s) pyrrolidin-2-yl) phenoxy] -4-chlorobenzene?
To prepare 1- [3- ((2S) -pyrrolidine-2-yl) phenoxy] - 4-chlorobenzene, there are many methods for its synthesis. Today, one of the methods is described as follows:
Starting materials, 3-hydroxyacetophenone and (2S) -pyrrolidine-2-formic acid can be selected, and (2S) -pyrrolidine-2-formic acid is first combined with appropriate reagents, such as sulfinyl chloride, to form (2S) -pyrrolidine-2-formyl chloride. In this step, thionyl chloride and (2S) -pyrrolidine-2-formic acid are added to the reaction flask in an appropriate ratio, such as 1.2:1, and stirred at room temperature for a number of times. When the reaction is complete, (2S) -pyrrolidine-2-formyl chloride is obtained.
Then, 3-hydroxyacetophenone is reacted with the acid chloride obtained above. Using triethylamine as the acid binding agent, the two are stirred under an ice bath in a suitable organic solvent, such as dichloromethane, and the solution of (2S) -pyrrolidine-2-formyl chloride is added dropwise. After adding dropwise, raise to room temperature, and continue to stir for the reaction number. After the reaction is completed, quench the reaction with dilute hydrochloric acid, separate the solution, dry the organic phase with anhydrous sodium sulfate, and remove the solvent by rotary evaporation to obtain an intermediate.
Then react this intermediate with 4-chlorobrombenzene. The reaction is heated and refluxed in N, N-dimethylformamide solvent with potassium carbonate as a base and copper powder as a catalyst. In this reaction, the intermediate, 4-chlorobrombenzene, potassium carbonate and copper powder are mixed in a suitable ratio, such as 1:1.2:2:0.1. After the reaction is completed, it is cooled, filtered, the filtrate is extracted with ethyl acetate, the organic phase is washed with water, dried, and evaporated. The crude product is purified by column chromatography to obtain the target product 1- [3- (2S) -pyrrolidine-2-yl) phenoxy] -4 -chlorobenzene.
However, the synthesis method is not limited to this one, and the combination of different starting materials and reaction conditions can be used to form this compound. It is necessary to choose the best one according to the specific situation of the experiment.
Starting materials, 3-hydroxyacetophenone and (2S) -pyrrolidine-2-formic acid can be selected, and (2S) -pyrrolidine-2-formic acid is first combined with appropriate reagents, such as sulfinyl chloride, to form (2S) -pyrrolidine-2-formyl chloride. In this step, thionyl chloride and (2S) -pyrrolidine-2-formic acid are added to the reaction flask in an appropriate ratio, such as 1.2:1, and stirred at room temperature for a number of times. When the reaction is complete, (2S) -pyrrolidine-2-formyl chloride is obtained.
Then, 3-hydroxyacetophenone is reacted with the acid chloride obtained above. Using triethylamine as the acid binding agent, the two are stirred under an ice bath in a suitable organic solvent, such as dichloromethane, and the solution of (2S) -pyrrolidine-2-formyl chloride is added dropwise. After adding dropwise, raise to room temperature, and continue to stir for the reaction number. After the reaction is completed, quench the reaction with dilute hydrochloric acid, separate the solution, dry the organic phase with anhydrous sodium sulfate, and remove the solvent by rotary evaporation to obtain an intermediate.
Then react this intermediate with 4-chlorobrombenzene. The reaction is heated and refluxed in N, N-dimethylformamide solvent with potassium carbonate as a base and copper powder as a catalyst. In this reaction, the intermediate, 4-chlorobrombenzene, potassium carbonate and copper powder are mixed in a suitable ratio, such as 1:1.2:2:0.1. After the reaction is completed, it is cooled, filtered, the filtrate is extracted with ethyl acetate, the organic phase is washed with water, dried, and evaporated. The crude product is purified by column chromatography to obtain the target product 1- [3- (2S) -pyrrolidine-2-yl) phenoxy] -4 -chlorobenzene.
However, the synthesis method is not limited to this one, and the combination of different starting materials and reaction conditions can be used to form this compound. It is necessary to choose the best one according to the specific situation of the experiment.
What is the price range for 1- [3- ((2s) pyrrolidin-2-yl) phenoxy] -4-chlorobenzene in the market?
I don't know what the price range is 1-%5B3-%28%282s%29pyrrolidin-2-yl%29phenoxy%5D-4-chlorobenzene the market. This compound may be a relatively uncommon chemical substance, and its price is determined by many factors, such as purity, yield, market demand, and difficulty in preparation.
If it is a commonly used chemical reagent, it may be available from general chemical reagent suppliers, and its price may vary according to specifications and purity. High purity is often more expensive, because the preparation process requires more complex purification processes, which consume more resources and energy.
If this is a special synthesis intermediate, which is only used in specific research or production processes, its price may vary depending on the cost of custom synthesis. Custom synthesis involves specialized synthesis route design, experimental operation and quality control, and the cost will increase.
The market supply and demand relationship also affects its price. If demand is strong and supply is limited, prices will rise; conversely, when supply exceeds demand, prices may fall. To know the exact price range, consult a professional chemical reagent dealer, a chemical product trading platform, or a relevant manufacturer, who can provide accurate price information based on real-time market conditions and specific product specifications.
If it is a commonly used chemical reagent, it may be available from general chemical reagent suppliers, and its price may vary according to specifications and purity. High purity is often more expensive, because the preparation process requires more complex purification processes, which consume more resources and energy.
If this is a special synthesis intermediate, which is only used in specific research or production processes, its price may vary depending on the cost of custom synthesis. Custom synthesis involves specialized synthesis route design, experimental operation and quality control, and the cost will increase.
The market supply and demand relationship also affects its price. If demand is strong and supply is limited, prices will rise; conversely, when supply exceeds demand, prices may fall. To know the exact price range, consult a professional chemical reagent dealer, a chemical product trading platform, or a relevant manufacturer, who can provide accurate price information based on real-time market conditions and specific product specifications.
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