Chemical Formula | C7H7ClFN |
Molecular Weight | 159.59 |
Appearance | Typically a colorless to light - colored liquid or solid (depending on conditions) |
Boiling Point | Data may vary, but generally in the range relevant to organic amines with similar structure |
Solubility In Water | Low solubility in water as it is an organic compound with non - polar aromatic and hydrophobic groups |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate |
Density | Specific density related to its molecular structure and packing in the liquid or solid state |
Flash Point | Flash point exists which is important for safety in handling as it is flammable in presence of heat and oxygen |
Pka | Characteristic pKa value related to the basicity of the amine group |
Chemical Formula | C7H7ClFN |
Appearance | Typically a colorless to light - colored liquid |
Boiling Point | Varies (approximate range might be around 200 - 230 °C under normal pressure) |
Solubility | Soluble in organic solvents like ethanol, dichloromethane, etc., poorly soluble in water |
Density | Approximate density around 1.2 - 1.3 g/cm³ |
Flash Point | Caution, flammable, flash point likely in the range of 70 - 90 °C |
Purity | Can be produced with high purity, e.g., 95%+ in commercial products |
Odor | May have a characteristic amine - like odor |
What are the physical properties of 2-Chloro-5-fluorobenzylamine?
2-Chloro-5-fluorobenzamine is a kind of organic compound. Its physical properties are unique, and it is mostly liquid at room temperature. Looking at its color, it is usually colorless to light yellow, and when it is pure, there should be no visible impurities.
Smell its smell, there is a specific amine smell, such smell may have a pungent feeling, and it is volatile in the air. The value of its boiling point is about a specific range, but the exact value depends on the experimental conditions and measurement methods, roughly between several degrees Celsius. The boiling point is affected by the intermolecular forces, and there are hydrogen bonds and van der Waals forces between the molecules of this compound.
When it comes to the melting point, there are also corresponding values, which reflect the arrangement of the molecular lattice. The melting point is closely related to the molecular structure, and the degree of molecular arrangement in the solid lattice determines the melting point.
In terms of solubility, 2-chloro-5-fluorobenzamine has good solubility in organic solvents, such as ethanol, ether, etc., because the molecular structure is consistent with the principle of similar miscibility in organic solvents. However, the solubility in water is limited, because of the difference between molecular polarity and water molecular polarity, it can only be dissolved in a small amount.
In terms of density, there is a certain value, which is larger or smaller than the density of water, depending on the molecular mass and the degree of compactness of intermolecular accumulation. Density is one of the characteristics of substances and is quite important in the calculation of separation, purification and related chemical reactions.
In conclusion, the physical properties of 2-chloro-5-fluorobenzamine are of great significance in chemical research and practical applications. Understanding these properties can help to better utilize this compound in organic synthesis, drug development, and other fields.
What are the chemical properties of 2-Chloro-5-fluorobenzylamine?
2-Chloro-5-fluorobenzyl amine is a class of organic compounds and plays a key role in the field of organic synthesis. This compound contains chlorine, fluorine and benzylamine groups, each of which is endowed with its unique chemical properties.
In terms of reactivity, the amino group of the benzylamine part is nucleophilic. This amino group easily reacts with many electrophilic reagents, such as halogenated hydrocarbons, acyl halides, etc. For example, it can undergo nucleophilic substitution reactions with halogenated hydrocarbons to form new carbon-nitrogen bonds, thereby constructing more complex organic molecular structures. The mechanism of this reaction is that the nitrogen atom of the amino group attacks the carbon atom of the halogenated hydrocarbon by virtue of its lone pair electrons, and the halogen atom is separated as a leaving group, and finally generates new compounds.
Furthermore, the presence of chlorine and fluorine atoms also significantly affects their chemical properties. Fluorine atoms are extremely electronegative, which can reduce the electron cloud density of the benzene ring through induction effects. This property changes the activity of the benzene ring for electrophilic substitution reactions, and is more prone to nucleophilic substitution reactions than the analogues without fluorine substitution. The chlorine atom, although less electronegative than the fluorine atom, also affects the electron cloud distribution of the benzene ring, and it can also participate in some substitution reactions. For example, under appropriate reaction conditions, chlorine atoms can be replaced by other nucleophiles to achieve functional group conversion.
In addition, the physical properties of 2-chloro-5-fluorobenzyl amine are also closely related to its chemical structure. Because it contains polar amino groups, it can be soluble in polar solvents, such as alcohols, ethers and other organic solvents to a certain extent. This solubility characteristic provides a corresponding basis and limitation for its use in organic synthesis operations, such as the selection of reaction solvents, the separation and purification of products.
Overall, 2-chloro-5-fluorobenzyl amine exhibits rich and diverse chemical properties due to its unique chemical structure, which shows broad application prospects and research value in the field of organic synthetic chemistry.
What are the main uses of 2-Chloro-5-fluorobenzylamine?
2-Chloro-5-fluorobenzyl amine is a key intermediate in organic synthesis. It has a wide range of uses and is particularly important in the field of medicinal chemistry.
First, it is often used to create new drugs. Because of its unique chemical structure, it can be used as a key building block to chemically synthesize with other compounds to construct molecules with specific pharmacological activities. In the development of anti-tumor drugs, using this as a starting material, through multi-step reactions, compounds can be prepared that can precisely act on specific targets of tumor cells, or can interfere with the growth and proliferation of tumor cells, and are expected to become anti-tumor drugs.
Second, it also has important applications in the field of pesticide chemistry. Based on 2-chloro-5-fluorobenzyl amine, pesticides with high insecticidal, bactericidal or herbicidal properties can be synthesized. Such pesticides can have a good control effect on crop diseases and pests, and because of their structural particularity, or low toxicity, environmental protection and other advantages, they have little impact on the environment and non-target organisms, which is in line with the current needs of green agriculture development.
Third, in the field of materials science, it may also have potential uses. After a specific chemical reaction, it can be introduced into the structure of polymer materials, giving new properties to the materials, such as improving the solubility, thermal stability or optical properties of the materials, thereby expanding the application range of materials in different fields.
In conclusion, 2-chloro-5-fluorobenzyl amine, with its unique chemical structure, is an indispensable synthetic intermediate in many fields such as medicine, pesticides and materials, and plays a crucial role in promoting the development of related fields.
What are 2-Chloro-5-fluorobenzylamine synthesis methods?
To prepare 2-chloro-5-fluorobenzyl amine, there are many methods, and the main ones are selected.
First, 2-chloro-5-fluorobenzoic acid is used as the beginning, and the carboxyl group is first chlorinated to convert to acid chloride. The reagents used are often dichlorosulfoxide and the like. This step is violent, and temperature control is required to prevent side effects. Following the method of ammonolysis, the acid chloride is interacted with excess concentrated ammonia water and replaced by nucleophilic substitution to produce 2-chloro-5-fluorobenzamide. Then a strong reducing agent such as lithium aluminum hydride is used to reduce the carbonyl group of the amide to methylene in an anhydrous ether and other solvents, and the target 2-chloro-5-fluorobenzyl amine is obtained. This route step is slightly complicated, but the reaction of each step is more mature and the yield is acceptable.
Second, 2-chloro-5-fluorobenzyl halogen (such as 2-chloro-5-fluorobenzyl chloride) is used as the starting material. It undergoes nucleophilic substitution with potassium phthalimide in a polar solvent (such as N, N-dimethylformamide), and the halogen atom of benzyl halogen is replaced by a phthalimide group. The product undergoes basic hydrolysis, the phthalimide group is removed, and it is converted into an amino group to obtain 2-chloro-5-fluorobenzyl amine. This way is relatively simple, but the starting benzyl halogen raw material needs to be prepared, and the appropriate conditions need to be selected for nucleophilic substitution to increase the yield.
Third, if 2-chloro-5-fluorobenzaldehyde is used as the raw material, it can be reacted with hydroxylamine hydrochloride first to obtain 2-chloro-5-fluorobenzaldehyde oxime. In the presence of a suitable catalyst (such as Raney nickel, etc.), the oxime is reduced with hydrogen to convert the oxime group into an amino group, and 2-chloro-5-fluorobenzyl amine can also be obtained. This path requires controlled reduction conditions to ensure that the reaction is complete and does not cause excessive reduction to produce by-products.
All these methods have advantages and disadvantages. In actual synthesis, the choice should be weighed according to factors such as raw material availability, cost, equipment conditions and product purity.
2-Chloro-5-fluorobenzylamine need to pay attention to when storing and transporting
2-Chloro-5-fluorobenzyl amine is an organic compound. When storing and transporting it, all matters need to be taken care of.
First words storage. This substance should be placed in a cool, dry and well-ventilated place. Cover because of its certain chemical activity, if it is in a high temperature and humid environment, it may cause chemical reactions and cause it to deteriorate. The warehouse temperature should be controlled within a specific range, such as not exceeding 30 degrees Celsius, and the humidity should not be too high to ensure its chemical stability. And it needs to be separated from oxidants, acids, bases and other substances, because it is easy to react with such substances, or even cause danger. The storage place should be equipped with suitable materials to contain leaks, so that they can be disposed of in time in case of accidental leakage.
As for transportation, it is necessary to ensure that the packaging is intact. Packaging materials should have good sealing and corrosion resistance, and can resist general external forces and chemical erosion. During transportation, vehicles should run smoothly to avoid severe vibration and collisions to prevent material leakage caused by package rupture. At the same time, the transportation environment should also follow the storage temperature and humidity requirements. Transportation personnel should be familiar with the characteristics of this substance and emergency treatment methods. In case of leakage and other emergencies, they can respond quickly and properly. And transportation related documents must be complete, clearly indicating key information such as material characteristics, hazards and emergency measures, so that personnel in all links can know.