4 Fluoro Benzenemethanamin
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
4-fluoro-benzenemethanamin
Chemical Formula C7H8FN
Molecular Weight 125.14
Appearance Typically a colorless to pale - yellow liquid
Boiling Point Approximately 185 - 187°C
Density Around 1.1 g/cm³ (estimated)
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether, etc.
Vapor Pressure Low at room temperature
Flash Point Around 70 - 80°C (estimated)
Odor Aminelike, pungent odor
Stability Stable under normal conditions but can react with strong oxidizing agents
Name 4-fluoro-benzenemethanamin
Molecular Formula C7H8FN
Molecular Weight 125.14
Chemical Formula C7H8FN
Appearance Solid or liquid (depends on conditions)
Melting Point Data needed
Boiling Point Data needed
Density Data needed
Solubility In Water Low (organic compound, non - polar nature)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point Data needed
Vapor Pressure Data needed
Pka Data needed
FAQ

What is the chemistry of 4-fluoro-benzenemethanamin?

4-Fluoro-benzenemethanamine is 4-fluorobenzamine, which is an organic compound. Its shape is usually colorless to light yellow liquid, with a unique odor of amines.

From a chemical point of view, 4-fluorobenzamine is basic because it contains amino groups (-NH ²). The nitrogen atom of the amino group has lone pairs of electrons, which can bind protons (H 🥰). In acidic solutions, it can react with acids to form salts. For example, it reacts with hydrochloric acid to form a corresponding hydrochloride salt. This property makes 4-fluorobenzamine soluble in acidic aqueous solutions.

The amino group of 4-fluorobenzamine is nucleophilic. In organic synthesis, it can participate in nucleophilic substitution reactions. Taking halogenated hydrocarbons as an example, the nitrogen atom of the amino group will attack the carbon atom of the halogenated hydrocarbon, and the halogen atom will leave to form a new nitrogen-containing compound, through which a variety of organic molecular structures can be constructed.

The benzene ring in its molecule also affects its chemical properties. The benzene ring has a conjugated system and is relatively stable. However, the benzene ring can undergo electrophilic substitution reaction. Due to the positioning effect of fluorine atoms and amino groups, electrophilic reagents mainly attack specific positions of the benzene ring. The fluorine atom belongs to the ortho-and para-site group, and the amino group is also the ortho-and para-site group. The two interact together, so that the electrophilic substitution reaction mostly occurs in the relatively suitable position of the benzene ring with the fluorine atom and the amino group, such as the orth The chemical properties of 4-fluorobenzamine make it widely used in the fields of medicine, pesticides and materials. In pharmaceutical synthesis, or as a key intermediate, it is used to prepare drug molecules with specific biological activities; in the field of pesticides, or participate in the synthesis of pesticide ingredients with insecticidal and bactericidal effects.

What are the main uses of 4-fluoro-benzenemethanamin?

4-Fluoro-benzenemethanamine is 4-fluorobenzamine, which has a wide range of uses. In the field of medicinal chemistry, it is a key intermediate for the synthesis of many drugs. The introduction of fluorine atoms can significantly change the physical, chemical and biological activities of compounds. Based on this, compounds with specific pharmacological activities can be prepared, or they can act on specific targets, which is helpful for the treatment of diseases such as tumors and neurological disorders.

In the field of materials science, 4-fluorobenzamine is also useful. Can participate in the synthesis of special polymers or functional materials. Due to its structure containing amino groups and benzene rings, it can react with other monomers to form polymeric materials with unique properties, such as strengthening the mechanical properties of materials, improving their thermal stability or endowing them with special optical and electrical properties.

In the field of organic synthetic chemistry, 4-fluorobenzamine is an important building block for organic synthesis. With the reactivity of amino groups, many chemical reactions can be carried out, such as reacting with acid chloride to form amides, or reacting with aldides and ketones to form imines, etc., to construct more complex and diverse organic compounds, which contribute to the development of organic synthetic chemistry.

Furthermore, in the fine chemical industry, 4-fluorobenzamine can be used to prepare special surfactants, flavors or additives. After reasonable chemical modification, the product can give unique properties and meet the special needs of fine chemicals in different fields.

What is 4-fluoro-benzenemethanamin synthesis method?

The method of synthesizing 4-fluoro-benzenemethanamine can follow the following steps.

First, 4-fluorobenzoic acid is used as the starting material. 4-fluorobenzoic acid is reacted with sulfuryl chloride (SOCl ²). In this reaction, sulfuryl chloride can convert carboxyl groups (-COOH) to acyl chloride (-COCl) to generate 4-fluorobenzoyl chloride. The reaction conditions are relatively mild, usually under the condition of heating and refluxing, the reaction can be completed in several hours, and the reaction yield is high.

Subsequently, the generated 4-fluorobenzoyl chloride is reacted with ammonia (NH 🥰). In this step, ammonia attacks the carbonyl carbon of the acid chloride as a nucleophilic reagent, and a nucleophilic substitution reaction occurs, thereby converting the acyl chloride group into an amide group to obtain 4-fluorobenzamide. The reaction is generally carried out at low temperature to avoid side reactions, and the yield can be improved by controlling the amount of ammonia and the reaction time.

Finally, the reduction reaction of 4-fluorobenzamide is carried out. The commonly used reducing agent is lithium aluminum hydride (LiAlH). In organic solvents such as anhydrous ether, lithium aluminum hydride can reduce the carbonyl group in the amide to methylene, thereby obtaining the target product 4-fluorobenzamide. The reaction needs to be carried out under strict anhydrous and oxygen-free conditions to ensure the smooth progress of the reaction and the purity of the product.

Another synthetic route can be started from 4-fluorobrobenzene. First, 4-fluorobrobenzene reacts with magnesium (Mg) in anhydrous ether to form Grignard's reagent 4-fluorophenylmagnesium bromide. After that, the Grignard reagent reacts with formaldehyde (HCHO) to generate 4-fluorobenzyl alcohol. Then 4-fluorobenzyl alcohol reacts with dichlorosulfoxide (SOCl ²) to convert hydroxyl (-OH) into chlorine atoms (-Cl) to obtain 4-fluorobenzyl chloride. Finally, 4-fluorobenzyl chloride reacts with ammonia (NH), the nitrogen atom in ammonia attacks the carbon atom of benzyl chloride, and a nucleophilic substitution reaction occurs, and finally 4-fluorobenzamine is formed. This method has relatively many steps, but the reaction conditions of each step are relatively mature, and the yield can be controlled within a certain range.

4-fluoro-benzenemethanamin What are the precautions in storage and transportation?

4-Fluoro-benzenemethanamine is an organic compound. During storage and transportation, the following matters should be paid attention to:

One is the storage temperature. This compound should be stored in a cool and ventilated warehouse. If the temperature is too high, it may increase its volatilization, or even cause a chemical reaction and cause quality changes. Therefore, the warehouse temperature should be controlled in a specific range, generally not exceeding 30 ° C.

The second is to avoid light. 4-Fluorobenzamine is more sensitive to light. Long-term light exposure may cause photochemical reactions to cause its structure to change, affecting its chemical properties and quality. Therefore, when storing, it should be placed in a dark place, or stored in an opaque container.

The third is to isolate fire and heat sources. Because of its certain flammability, in case of open flame, hot topic or cause combustion or even explosion. Fireworks are strictly prohibited around the warehouse, and all kinds of heat sources should be kept away, such as heating, steam pipes, etc.

The fourth is the choice of storage containers. Corrosion-resistant and well-sealed containers should be used. 4-Fluorobenzamine or chemical reaction with some materials, erosion of the container, causing leakage. Generally, containers made of glass, stainless steel and other materials can be used.

In terms of transportation, the first thing to ensure is that the packaging is intact. Appropriate packaging materials and methods should be used in accordance with relevant regulations to ensure that the packaging is not damaged or leaked during transportation.

Furthermore, the transportation vehicle shall be equipped with corresponding fire protection equipment and leakage emergency treatment equipment. In the event of a leak, it can be responded to in time to reduce the harm.

And the transportation process should be far away from densely populated areas and important facilities. In the event of an accident, the impact on the public and important facilities can be reduced.

Transportation personnel also need to be professionally trained to be familiar with the characteristics of 4-fluorobenzamine and emergency treatment methods. In this way, the safety of storage and transportation can be guaranteed to avoid accidents.

4-fluoro-benzenemethanamin impact on the environment and human health

4-Fluoro-benzenemethanamine is 4-fluorobenzamine, which is an organic compound. Regarding its impact on the environment and human health, let me know in detail.

At the environmental level, if 4-fluorobenzamine is released into the environment, it will have many effects. In water, because of its certain chemical activity, it may interfere with the normal physiological processes of aquatic organisms. For example, it may change the permeability of the cell membrane of aquatic organisms, causing abnormal exudation of intracellular substances or abnormal entry of external harmful substances, thereby affecting the growth, reproduction, and even survival of aquatic organisms. In the soil, it may react chemically with various minerals and organic matter in the soil, changing the chemical properties of the soil and affecting the structure and function of the soil microbial community. For example, inhibiting the growth of certain microorganisms that are crucial to the improvement of soil fertility, which in turn affects the absorption of nutrients by plants, and ultimately affects the balance of the entire ecosystem.

In terms of human health, 4-fluorobenzamine also has potential hazards. It may be irritating. If it comes into contact with the skin, it may cause skin redness, swelling, itching, pain and other symptoms, and even cause skin burns in severe cases. If it is not carefully entered into the eyes, it will cause great damage to the eye tissue, causing severe eye pain, tears, blurred vision, and even damage the cornea of the eye, affecting vision. Inhalation of its vapors in the air can irritate the respiratory tract, causing symptoms such as cough, asthma, and breathing difficulties. Long-term or heavy inhalation may cause persistent damage to the respiratory mucosa, increasing the risk of respiratory diseases. If taken by mistake, it will damage the digestive system, cause symptoms such as nausea, vomiting, abdominal pain, diarrhea, and even cause substantial damage to internal organs.

In conclusion, 4-fluorobenzamide poses a potential threat to both the environment and human health. When producing, using and handling this substance, it is necessary to be cautious and take comprehensive protective and disposal measures to reduce its adverse effects on the environment and human health.