Chemical Formula | C6H4ClF3N2 |
Molecular Weight | 196.56 |
Appearance | Solid (usually white to off - white powder) |
Melting Point | Typically in a certain range (e.g., around 100 - 110°C, actual may vary) |
Solubility In Water | Low solubility in water |
Solubility In Organic Solvents | Soluble in some organic solvents like dichloromethane, ethyl acetate |
Density | Calculated density with a certain value (e.g., around 1.4 - 1.5 g/cm³, approximate) |
Pka Value | Specific pKa value related to its amine group (e.g., around 4 - 5, approximate) |
Flash Point | Necessary to be cautious about flammability, flash point in a certain range (e.g., around 100 - 120°C, approximate) |
Chemical Formula | C6H4ClF3N2 |
Molar Mass | 196.56 g/mol |
Appearance | Typically a solid |
Physical State | Solid at standard conditions |
Solubility In Water | Low solubility (amine group can have some interaction but trifluoromethyl and chloro groups reduce it) |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
Odor | May have a characteristic amine - like odor |
Pka | Related to the basicity of the amine group, but specific value requires research |
Stability | Stable under normal conditions, but may react with strong acids, bases, or oxidizing agents |
Chemical Formula | C6H4ClF3N2 |
Molecular Weight | 196.56 |
Appearance | Solid (usually white to off - white) |
Odor | Typically has a characteristic amine - like odor |
Melting Point | Data may vary, but around [specific value if known] °C |
Boiling Point | Data may vary, but around [specific value if known] °C |
Solubility In Water | Limited solubility, [approximate value if known] g/L |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, acetone |
Density | [Specific value if known] g/cm³ |
Pka Value | [Value if known] (related to its basicity) |
Stability | Stable under normal conditions, but may react with strong oxidizing agents |
Chemical Formula | C6H4ClF3N2 |
Molecular Weight | 196.56 |
Appearance | Solid (usually white or off - white powder) |
Melting Point | Data may vary depending on purity, typically in a certain range |
Solubility In Water | Low solubility in water |
Solubility In Organic Solvents | Soluble in some organic solvents like dichloromethane, chloroform |
Odor | May have a characteristic, somewhat pungent odor |
Density | Data may be available based on experimental determination |
Stability | Should be stored in a cool, dry place away from oxidizing agents, relatively stable under normal conditions |
What are the chemical properties of 3-chloro-5-trifluoromethyl-2-pyridylamine?
3-Chloro-5-trifluoromethyl-2-pyridylamine, an organic compound, is widely used in the field of organic synthesis.
Looking at its physical properties, it is mostly solid at room temperature and pressure, but the specific properties will vary depending on the purity and crystallization. Its melting point, boiling point and density data can be accurately determined under specific conditions. Generally speaking, this substance may have some solubility in common organic solvents, such as ethanol, ether, dichloromethane, etc., while its solubility in water is relatively limited.
As for its chemical properties, the chlorine atoms in its molecules are quite active. The chlorine atom is connected to the pyridine ring, and is affected by the electronic effect of the pyridine ring, which makes it more prone to nucleophilic substitution reactions. For example, when encountering nucleophilic reagents, such as sodium alcohol and amines, chlorine atoms may be replaced to form a series of derivatives. This reaction is widely used in the preparation of new compounds in organic synthesis.
Furthermore, the presence of amino groups also endows the compound with unique chemical properties. Amino groups are basic and can neutralize with acids to generate corresponding salts. In organic reactions, amino groups can also participate in reactions as nucleophilic reagents, such as acylation reactions with acyl halides, acid anhydrides, etc., to form amide compounds.
The introduction of trifluoromethyl groups greatly changes the electron cloud distribution and spatial structure of molecules. Trifluoromethyl groups have strong electron-absorbing properties, which reduce the electron cloud density of pyridine rings, which not only affects the activity and selectivity of substitution reactions on the ring, but also has significant effects on the stability, fat solubility and biological activity of the whole molecule. For example, due to the strong electron-absorbing effect of trifluoromethyl groups, or the special properties of the compound in some biological activity tests, it has attracted much attention in the fields of medicine and pesticide research and development.
What are the main uses of 3-chloro-5-trifluoromethyl-2-pyridylamine?
3-Chloro-5-trifluoromethyl-2-pyridylamine is an important organic compound that is widely used in many fields.
First, in the field of medicinal chemistry, this compound is often a key intermediate for the synthesis of new drugs. Due to its special chemical structure, it can interact with specific targets in organisms and has potential pharmacological activity. Chemists can create drugs with unique curative effects by modifying and modifying their structures, such as treating drugs for specific diseases, or improving the performance of existing drugs, enhancing curative effect and reducing side effects.
Second, in the field of pesticide chemistry, 3-chloro-5-trifluoromethyl-2-pyridylamine also plays an important role. It can be used as a raw material for the synthesis of high-efficiency and low-toxicity pesticides. Due to the presence of chlorine atoms and trifluoromethyl in its structure, the compound has certain insecticidal, bactericidal or herbicidal activities. Through rational design and synthesis, pesticides with good control effect on crop diseases and insect pests can be developed, which can help increase agricultural production and income, and can reduce the harm to the environment.
Furthermore, in the field of materials science, this compound can also play a role. It can participate in the synthesis of certain functional materials, such as materials with special optical, electrical or thermal properties. Due to its unique structure, it may introduce special properties into materials to meet the special needs of different fields for material properties, such as electronic devices, optical devices and other fields.
In short, 3-chloro-5-trifluoromethyl-2-pyridylamine has shown important application value in many fields such as medicine, pesticides and materials science due to its unique chemical structure, providing a key material basis and research direction for the development of related fields.
What is 3-chloro-5-trifluoromethyl-2-pyridylamine synthesis method?
To prepare 3-chloro-5-trifluoromethyl-2-pyridylamine, the common method is as follows.
The starting material is 3-chloro-5-trifluoromethyl-pyridine, which can be reacted with an appropriate nucleophilic reagent first. Taking ammonia or amine reagents as an example, under suitable reaction conditions, the nitrogen atom in ammonia or amine launches a nucleophilic attack on the carbon atom at the 2-position on the pyridine ring by virtue of its lone pair electrons. This step requires attention to the reaction temperature, reaction time, and molar ratio of the reactants. Generally speaking, temperature control is very critical. If it is too low, the reaction rate will be slow, and if it is too high, it will cause more side reactions.
If liquid ammonia is used as a nucleophilic reagent, react under a certain pressure and temperature in an autoclave. The pressure may need to be maintained at several megapascals, and the temperature may be between tens of degrees Celsius and hundreds of degrees Celsius. By precisely regulating these conditions, the reaction is promoted towards the direction of generating the target product 3-chloro-5-trifluoromethyl-2-pyridylamine.
Or 3-chloro-5-trifluoromethylpyridine is activated first, for example, converted into a more active intermediate, and then reacted with the nucleophilic reagent. This may reduce the rigor of the reaction conditions and improve the selectivity and yield of the reaction. After the
reaction is completed, the separation and purification of the product is also an important step. Methods such as extraction, distillation, and column chromatography can be used. During extraction, a suitable extractant is selected according to the difference in solubility of the product and impurities in different solvents. Distillation is separated by the different boiling points of each substance. Column chromatography can utilize the difference in the adsorption capacity of the adsorbent to different substances to achieve effective separation of the product and impurities, and finally obtain high-purity 3-chloro-5-trifluoromethyl-2-pyridylamine.
3-chloro-5-trifluoromethyl-2-pyridylamine what are the precautions during storage and transportation?
3-Chloro-5-trifluoromethyl-2-pyridylamine is a chemical substance. When storing and transporting, many key matters need to be paid attention to to to ensure its quality and safety.
When storing, the first environment is heavy. Choose a cool, dry and well-ventilated place, away from fire and heat sources. This is because the substance may be flammable, and the high temperature environment is prone to danger. The warehouse temperature should be controlled within a specific range, such as not exceeding 30 ° C, and the humidity should not exceed 80% to prevent deterioration.
Furthermore, it needs to be stored in separate zones with different types of chemicals. Do not mix with oxidizing agents, acids, alkalis, etc., due to violent chemical reactions with each other, causing explosions or the formation of harmful substances.
Packaging is also crucial. Be sure to ensure that the packaging is intact and tightly sealed to prevent leakage. Common sealed barrels or special packaging materials are used to ensure safety.
During transportation, there are also many points. Transportation vehicles need to be equipped with corresponding fire fighting equipment and leakage emergency treatment equipment. When driving, avoid densely populated areas and busy traffic sections to prevent accidental leakage from endangering the public.
The loading and unloading process should be handled with care. It is strictly forbidden to drop and heavy pressure to avoid packaging damage. Staff should wear appropriate protective equipment, such as protective clothing, gloves and goggles, to avoid direct contact.
In the event of a leak, the surrounding people should be evacuated quickly to isolate the leak area. Emergency responders need to wear professional protective equipment and do not let the leak come into contact with fire sources or oxidants. Small leaks can be absorbed by inert materials such as sand and vermiculite; large leaks need to be built embankment or dug for containment, and transferred to a special container with an explosion-proof pump.
In summary, the storage and transportation of 3-chloro-5-trifluoromethyl-2-pyridylamine should be treated with caution and operated in strict accordance with regulations to ensure safety.
What are the effects of 3-chloro-5-trifluoromethyl-2-pyridylamine on the environment and human health?
3-Chloro-5-trifluoromethyl-2-pyridylamine is one of the organic compounds. The impact on the environment and human health cannot be ignored.
As far as the environment is concerned, if this compound is released in nature, or due to chemical stability, it is difficult to be rapidly decomposed by microorganisms, resulting in long-term retention. In the soil, it may affect the soil quality, interfere with the absorption of nutrients by plants, or change the structure of soil microbial community, destroying the ecological balance. In the water body, it may harm aquatic organisms, cause abnormal physiological functions, and affect reproduction and survival.
As for human health, if this substance enters the human body through respiratory tract, skin contact or accidental ingestion, there may be a latent risk. May interfere with the human endocrine system, affect the normal secretion and regulation of hormones, and then cause a series of health problems, such as reproductive dysfunction, metabolic disorders, etc. Long-term exposure may damage the nervous system, causing symptoms such as headache, dizziness, memory loss, etc. And there is also a potential carcinogenic risk. Although it is not conclusive, it should not be taken lightly.
Therefore, the production, use and disposal of 3-chloro-5-trifluoromethyl-2-pyridylamine should be done with caution and proper measures should be taken to reduce its harm to the environment and human health, protect the safety of the ecological environment, and protect the health of the human body.