Chemical Formula | C12H17FN2O |
Molecular Weight | 224.27 |
Appearance | Solid (usually white or off - white) |
Physical State At Room Temperature | Solid |
Melting Point | Data may vary, but typically in the range of 50 - 70 °C |
Solubility In Water | Low solubility in water due to its organic nature |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate |
Density | Approx. 1.1 - 1.2 g/cm³ |
Flash Point | Estimated around 120 - 140 °C |
Chemical Formula | C12H17FN2O |
Molecular Weight | 224.274 g/mol |
Appearance | Solid (predicted) |
Boiling Point | 333.4°C at 760 mmHg (predicted) |
Melting Point | N/A (no data found) |
Density | 1.136 g/cm³ (predicted) |
Flash Point | 155.4°C (predicted) |
Solubility | Soluble in organic solvents like dichloromethane, methanol (predicted) |
Logp | 1.42 (predicted) |
Pka | 9.39 (predicted) |
What is the main use of 3-Aminomethy-4- (4-fluorobenzyl) morpholine?
3 - Aminomethy - 4 - (4 - fluorobenzyl) morpholine, Chinese name or 3 - aminomethyl - 4 - (4 - fluorobenzyl) morpholine. This substance has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry to facilitate the creation of new drugs. Because its structure contains nitrogen heterocycles and fluorobenzyl groups, it endows unique physical and biological activities. When developing antibacterial, anti-inflammatory, anti-tumor and other drugs, the modified structure can optimize the activity and selectivity, and contribute to the development of new drugs.
In the field of materials science, it also has important functions. Due to its special structure, it may improve the properties of materials. For example, in the preparation of polymer materials, this compound is introduced to improve the mechanical properties, thermal stability and chemical stability of materials, and is used to make high-performance engineering plastics, coatings, etc., to expand the application scenarios of materials.
In the field of organic synthesis, as a characteristic reagent or intermediate, it participates in various organic reactions, such as nucleophilic substitution, condensation reactions, etc., to help build complex organic molecular structures, provide new paths and possibilities for the development of organic synthesis chemistry, and promote technological innovation and progress in this field.
What are the physical properties of 3-Aminomethy-4- (4-fluorobenzyl) morpholine
3-Aminomethyl-4- (4-fluorobenzyl) morpholine, an organic compound, has attracted much attention in the fields of chemistry and medicine. Its unique physical properties have far-reaching implications for its applications.
Under normal temperature and pressure, it may be a colorless to pale yellow liquid. This color and state are conducive to observation and operation in specific reactions and preparations. Its odor may have a faint special smell. Although it is not strong and pungent, it needs to be disposed of in a well-ventilated environment to avoid irritation to the human respiratory tract.
When it comes to boiling point, the boiling point may be within a certain range due to the molecular structure and interaction forces. A higher boiling point means that at relatively high temperatures, the compound converts from liquid to gaseous state. This property is of great significance in distillation, separation and purification processes. The appropriate temperature can be selected accordingly to achieve effective separation of the substance from other components.
In terms of melting point, the temperature at which the solid and liquid states are converted has a great impact on storage and transportation. If the melting point is too low, it may be difficult to maintain the solid state at room temperature, and special storage conditions are required; if the melting point is too high, in some processing processes, higher temperatures are required to melt it, increasing energy consumption and operation difficulty.
Solubility is also key. The compound may have good solubility in organic solvents such as ethanol and dichloromethane. This property is convenient for use as a reactant or product in organic synthesis reactions, dissolved in specific solvents to participate in the reaction, and is conducive to separation and purification by extraction, crystallization and other means after the reaction. However, the solubility in water is poor, which needs to be taken into account in applications involving aqueous phase systems.
Density is another important physical property. When mixed with other substances, the density difference determines its distribution in the system, which has a significant impact on the mixing uniformity and phase separation process.
In addition, the vapor pressure of the compound cannot be ignored. Vapor pressure characterizes the difficulty of volatilization. When the vapor pressure is high, it is more volatile to the air at room temperature, which not only affects the stability of its content, but also may pose a potential threat to the environment and the health of operators.
The above physical properties are interrelated and comprehensively affect the application of 3-aminomethyl-4- (4-fluorobenzyl) morpholine in different fields. When researching and using, it is necessary to comprehensively consider in order to achieve the best effect and ensure safety.
What is the chemical synthesis method of 3-Aminomethy-4- (4-fluorobenzyl) morpholine?
The chemical synthesis of 3-aminomethyl-4- (4-fluorobenzyl) morpholine is a significant research in the field of chemistry. To synthesize this compound, the following steps can be followed.
In the selection of starting materials, morpholine derivatives should be used as the base. First, the morpholine is reacted with fluorobenzylated reagents under specific conditions. This reaction requires precise regulation of reaction conditions, such as temperature, solvent, catalyst and other factors. A suitable aprotic solvent, such as dichloromethane or N, N-dimethylformamide (DMF), is selected, and an appropriate amount of base, such as potassium carbonate or triethylamine, is added in the range between low temperature and room temperature to catalyze the reaction process, which promotes the successful introduction of fluorobenzyl into the specific position of morpholine to generate 4- (4-fluorobenzyl) morpholine intermediates.
Then, for the obtained 4- (4-fluorobenzyl) morpholine intermediates, the amino methyl group is to be introduced. It can be achieved by the nucleophilic substitution reaction of halogenated alkanes with ammonia or amines. First, 4 - (4 - fluorobenzyl) morpholine is mixed with a halomethyl reagent, such as chloromethylation reagent, in a suitable solvent, which can also be selected from dichloromethane or DMF. During the reaction, the temperature and reaction time are controlled, and a base is added to promote the reaction. After the reaction is completed, the product is separated and purified by an appropriate method, such as column chromatography, by means of a silica gel column, a suitable eluent is selected to obtain a pure 3 - aminomethyl - 4 - (4 - fluorobenzyl) morpholine product.
During the synthesis process, the precise control of the reaction conditions is the key, which is related to the purity and yield of the product. After each step of the reaction, the structures of intermediates and final products need to be identified in detail by means of analysis methods such as nuclear magnetic resonance (NMR) and mass spectrometry (MS) to ensure that the synthesis is correct. In this way, 3-aminomethyl-4- (4-fluorobenzyl) morpholine can be successfully synthesized.
What is the market price of 3-Aminomethy-4- (4-fluorobenzyl) morpholine?
There is a question today, what is the market price of 3-aminomethyl-4- (4-fluorobenzyl) morpholine. This is a question in the field of fine chemicals, and its price is determined by many factors.
First, the cost of raw materials is of great significance. The price fluctuations of raw materials required for the preparation of this compound, such as fluorobenzene, morpholine and other related reagents, will cause the cost of the product to change. If raw materials are scarce or the process of producing raw materials changes, the price of 3-aminomethyl-4- (4-fluorobenzyl) morpholine will also rise, and the market price will rise.
Second, the simplicity of the production process is closely related to the cost. If the preparation process is complex, multi-step reaction, special catalyst or harsh reaction conditions, such as high temperature, high pressure, inert gas protection, etc., will increase the production cost, and the market price will also be high. However, if the new process comes out, it can simplify the process, improve the yield, or reduce its cost and price.
Third, the market supply and demand situation has a significant impact. If the demand for this compound in the pharmaceutical, pesticide and other industries increases sharply, but the supply is limited, if the production enterprises are few and the production capacity is insufficient, the price will rise. On the contrary, if the market demand is low, the production enterprises may reduce the price in order to destock.
Fourth, regional differences cannot be ignored. In different regions, due to differences in economic level, logistics costs, and tax policies, prices are also different. In developed areas, or due to high operating costs, the selling price is relatively high; while in some chemical industry clusters, due to complete industrial chains, convenient logistics, cost reduction, and prices may be more accessible to the people.
In summary, the market price of 3-aminomethyl-4- (4-fluorobenzyl) morpholine ranges from hundreds of yuan per kilogram to thousands of yuan. It is difficult to determine an exact price. It needs to be judged comprehensively according to the above factors.
3-Aminomethy-4- (4-fluorobenzyl) morpholine in storage and transportation
For 3-aminomethyl-4- (4-fluorobenzyl) morpholine, all precautions must be kept in mind during storage and transportation.
This compound is sensitive or sensitive. When storing, make sure the environment is dry and cool. If the humidity is too high, it may cause deliquescence and deterioration, and if the temperature is too high, it may cause a chemical reaction, which will damage its purity and quality. Therefore, it should be placed in a well-ventilated place, protected from direct sunlight, and covered with ultraviolet rays in sunlight or can promote its decomposition.
When transporting, the packaging must be solid and reliable. To prevent vibration and collision from causing damage to the package and allowing the compound to leak. Selecting suitable packaging materials, such as corrosion-resistant containers, can ensure that it is not disturbed by external factors during transportation. And transportation vehicles should also maintain a stable environment to avoid large fluctuations in temperature and humidity.
In addition, this compound may be dangerous, and relevant operators must be professionally trained to know its characteristics and safe operation norms. Storage and transportation sites should be equipped with corresponding emergency treatment equipment and materials. In case of leakage and other accidents, they can be responded to quickly to reduce hazards. In this way, the safety and quality of 3-aminomethyl-4- (4-fluorobenzyl) morpholine during storage and transportation must be ensured.