Chemical Formula | C7H6F3NO2S |
Molar Mass | 225.19 g/mol |
Appearance | Solid (usually white or off - white) |
Melting Point | Data - specific value needed |
Boiling Point | Data - specific value needed |
Density | Data - specific value needed |
Solubility In Water | Low solubility, organic solvents - better solubility |
Vapor Pressure | Data - specific value needed |
Flash Point | Data - specific value needed |
Stability | Stable under normal conditions, may react with strong oxidizing agents |
Chemical Formula | C7H6F3NO2S |
Molecular Weight | 225.19 |
Appearance | Solid (usually white or off - white powder) |
Odor | May have a faint, characteristic odor |
Melting Point | Typically in a certain range (needs more precise data) |
Boiling Point | Requires specific experimental data |
Solubility In Water | Low solubility in water |
Solubility In Organic Solvents | Soluble in some organic solvents like dichloromethane |
Density | Needs experimental determination |
Flash Point | Data required from specific tests |
Pka | Relevant acid - base dissociation constant data needed |
Vapor Pressure | Value depends on temperature, data required |
Chemical Formula | C7H6F3NO2S |
Appearance | Typically a solid (description may vary) |
Solubility In Water | Low solubility, as it is an organic sulfonamide with fluorine substitution |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
Vapor Pressure | Low vapor pressure, being a relatively high - molecular - weight organic compound |
Stability | Stable under normal conditions, but may react with strong oxidizing or reducing agents |
Chemical Formula | C7H6F3NO2S |
Molar Mass | 225.19 g/mol |
Appearance | Solid (usually white or off - white) |
Melting Point | Typically in a certain range, data needed for exact value |
Boiling Point | Data required for accurate value |
Solubility In Water | Low solubility, hydrophobic |
Solubility In Organic Solvents | Soluble in some common organic solvents like dichloromethane |
Density | Data required for accurate value |
Flash Point | Data needed for exact value |
Pka | Data required for accurate value |
Stability | Stable under normal conditions, but may react with strong oxidizing agents |
What are the main uses of 1,1,1-trifluoro-N-phenylmethanesulfonamide?
1% 2C1% 2C1-triene-N-benzylacetamide, which is used in the field of pharmacology, has many special uses. It is often a key intermediate in pharmaceutical synthesis, and plays a significant role in the creation of antibacterial and anti-inflammatory drugs. Because of its structural characteristics, it can help drug molecules precisely fit the target and improve the efficacy.
In the past, pharmacists developed antibacterial agents, but there was no suitable material. Later, 1% 2C1% 2C1-triene-N-benzylacetamide was obtained, and a new molecular structure was constructed based on it. After repeated trials, a new type of antibacterial drug was formed, which has good effect on all kinds of bacteria and has minimal side effects. < Br >
And in the creation of anti-inflammatory drugs, also rely on this substance. It can regulate the pathway of the body's inflammatory response, block the release of inflammatory mediators, and slow down inflammatory symptoms. Doctors use it as medicine to treat rheumatism, arthritis and other inflammatory diseases, and the patient is relieved and gradually recovered.
Furthermore, in the art of organic synthesis, 1% 2C1% 2C1-triene-N-benzylacetamide is also a commonly used raw material. It can evolve various compounds with complex structures through various reactions, which is a new way for the research of organic chemistry and promotes the rise of new drugs and materials.
What are the synthesis methods of 1,1,1-trifluoro-N-phenylmethanesulfonamide?
To prepare 1% 2C1% 2C1-trifluoro-N-benzylacetamide, there are the following methods:
First, acetamide is used as the beginning, and then benzylated to obtain N-benzylacetamide, and then trifluoromethylated. However, in this way, when benzylated, there may be side reactions, resulting in impure products, and trifluoromethylation steps, harsh conditions, special reagents and equipment are required, and the operation is cumbersome.
Second, trifluoroacetyl derivatives are first prepared, and then reacted with benzylamine. In this way, the preparation of trifluoroacetyl derivatives requires specific raw materials and conditions, and when reacting with benzyl amines, there may be equilibrium problems, which affect the yield.
Third, the reaction of benzyl halide and trifluoroacetamide in the presence of a base. This process requires the selection of a base and a solvent to promote the reaction to generate the target product. However, the activity of benzyl halide or side reactions, such as elimination reaction.
Fourth, the coupling reaction catalyzed by transition metals can be used. The reaction of a halide containing trifluoromethyl or a pseudo-halide with a benzyl amine compound is catalyzed by a transition metal catalyst such as palladium and nickel. This approach has the advantages of high selectivity, but the catalyst cost is high, and the post-reaction treatment may be complicated.
All methods have their own advantages and disadvantages. In actual preparation, according to the availability of raw materials, cost, equipment conditions, and the requirements for product purity and yield, the appropriate method should be carried out.
What are the physical properties of 1,1,1-trifluoro-N-phenylmethanesulfonamide
1% 2C1% 2C1-triene-N-benzylacetamide, this physical property is quite specific. Its color state is often crystalline, and the texture is delicate and has a certain luster. Its shape, or needle-like or flake-like appearance, varies according to the method and conditions of synthesis.
Its melting point is a key indicator for measuring physical properties, and it is about a specific temperature range. At this temperature, the state of matter changes from solid to liquid, and this change is a characterization of the intermolecular force affected by temperature. The boiling point is also fixed. When it reaches a certain high temperature, the substance converts from liquid to gas. This process is related to the ability of the molecule to break free from the liquid phase. < Br >
In terms of solubility, it has a considerable solubility in organic solvents, such as ethanol and acetone. Due to the affinity of some groups in the molecular structure with organic solvents, they can be fused and mutually soluble by the interaction between molecules. However, the solubility of water is completely different. Due to the obvious hydrophobic tendency of the structure as a whole, it is difficult to dissolve in water.
The density is larger than that of water, and if placed in water, it will naturally settle. This is because the molecules are tightly packed and have a large mass per unit volume. And its stability is still good. It is not easy to change the structure under conventional environmental conditions, such as room temperature and pressure, and ordinary light. In the case of strong acids, strong bases, or high temperatures and strong oxidation, its structure may change, causing chemical changes. < Br >
Its refractive index also has characteristics. When light passes through, the degree of deflection of the light path is different from that of other substances due to the action of molecules inside the substance. This characteristic can be an important reference for the identification and analysis of substances.
What are the precautions for storing and transporting 1,1,1-trifluoro-N-phenylmethanesulfonamide?
1% 2C1% 2C1-trifluoro-N-benzylacetamide This material has many things to pay attention to during storage and transportation, as detailed below:
First, the storage environment must be carefully selected. Due to its nature, it may be sensitive to temperature and humidity, so it should be placed in a cool, dry and well-ventilated place. Do not store in a humid place to prevent deliquescence and other conditions caused by high environmental humidity, which will affect the quality. Temperature also needs to be strictly controlled. Excessive temperature may cause chemical reactions such as decomposition, which will damage its chemical structure and performance.
Second, the packaging must be solid and reliable during transportation. Appropriate packaging materials should be selected to ensure that the packaging will not be damaged due to collision and vibration during handling and loading and unloading. Packaging should be well sealed to prevent leakage, so as not to cause harm to the surrounding environment and personnel. At the same time, relevant warning labels should be clearly marked on the outside of the package, such as chemical categories, hazardous characteristics and other information, so that transporters and regulators can quickly identify and take appropriate protective measures.
Third, we must strictly follow relevant regulations and standards. Whether it is storage or transportation, it should comply with the chemical management norms formulated by the state and industry. Storage sites should be equipped with corresponding safety facilities, such as fire protection equipment, leakage emergency treatment equipment, etc.; transportation vehicles must also meet specific conditions, and drivers and escorts should have professional knowledge and qualifications, familiar with the characteristics of the chemical and emergency disposal methods.
Fourth, avoid contact with incompatible substances. During storage and transportation, be sure to avoid storing or transporting 1% 2C1% 2C1-trifluoro-N-benzylacetamide with substances that may react. For example, some strong oxidizing agents, strong acids, strong bases, etc., once they come into contact with each other, they are very likely to cause violent chemical reactions, resulting in dangerous accidents.
What are the effects of 1,1,1-trifluoro-N-phenylmethanesulfonamide on the environment and human health?
1% 2C1% 2C1-trifluoro-N-benzylacetamide has many effects on the environment and human health.
Looking at the environment, if this chemical substance is released into nature, it may play a complex role in the ecosystem. It may have certain residues and migration in soil and water. In soil, it may interfere with the balance of soil microbial communities, affect the transformation and circulation of substances in soil, such as nitrogen, phosphorus and other nutrient cycling processes, and then affect the growth and development of plants. In water bodies, or toxic to aquatic organisms, interfering with the physiological functions of aquatic organisms, such as affecting the respiration, reproduction and other behaviors of fish. In severe cases, the population of some aquatic organisms may decline, and the structure and function of aquatic ecosystems may be damaged.
As for human health, its potential harm cannot be ignored. If ingested in the human body through respiration, skin contact or diet, or accumulated in the body. Studies suggest that such fluorinated organic compounds may interfere with the human endocrine system, affect the synthesis, secretion and function of hormones, and thus have adverse effects on human metabolism, growth and development, and reproductive function. Long-term exposure or increased risk of certain diseases, such as affecting thyroid function, resulting in abnormal thyroid hormone secretion, leading to thyroid-related diseases; may also cause damage to the reproductive system, affect the quality and quantity of germ cells, and endanger fertility.
In short, 1% 2C1% 2C1-trifluoro-N-benzylacetamide poses a latent risk to the environment and human health, and needs to be treated strictly, and monitoring and control should be strengthened to reduce its adverse effects.