2 Chloro 1 4 Fluorophenyl Methyl 1h Benzimidazole
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-chloro-1-[(4-fluorophenyl)methyl]-1H-benzimidazole
Chemical Formula C14H10ClFN2
Molar Mass 260.696 g/mol
Appearance Typically a solid
Solubility In Water Low (organic compound, relatively non - polar)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Logp Positive (hydrophobic due to aromatic and fluorophenyl groups)
Chemical Formula C14H10ClFN2
Molar Mass 260.698 g/mol
Appearance Solid (usually white to off - white)
Melting Point Data may vary, typically in a specific temperature range
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane
Density Specific value depending on experimental conditions
Pka Value related to its acidic or basic character
Logp Measure of lipophilicity, specific value
Chemical Formula C14H10ClFN2
Molecular Weight 260.698 g/mol
Appearance Typically a solid (appearance can vary based on purity and preparation)
Melting Point Data may vary, needs specific experimental determination
Boiling Point Data may vary, needs specific experimental determination
Solubility Solubility characteristics depend on solvents; may have limited solubility in water, better solubility in organic solvents like ethanol, acetone etc.
Density Data may vary, needs specific experimental determination
Flash Point Data may vary, needs specific experimental determination
Vapor Pressure Data may vary, needs specific experimental determination
Stability Can be stable under normal conditions, but may react with strong oxidizing or reducing agents
Chemical Formula C14H10ClFN2
Molecular Weight 260.698 g/mol
Appearance Solid (usually white or off - white powder)
Melting Point Typically in a certain range (data may vary, e.g., around 180 - 190°C)
Solubility Poorly soluble in water, soluble in some organic solvents like DMSO, DMF
Density Data may vary, typical range for organic solids
Logp Indicative of lipophilicity, data may vary
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
FAQ

What are the physical properties of 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole

2-Chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole is a kind of organic compound. The physical properties of this compound are related to its appearance, melting point, boiling point, solubility and other characteristics, which are quite important in chemical research and practical application.

Look at its appearance at room temperature and pressure, or in the form of white to light yellow crystalline powder. This form is conducive to its storage and transportation, and in many chemical reactions, the powdered substance can provide a larger reaction contact area and promote the reaction.

The melting point is the temperature at which the substance changes from a solid state to a liquid state. The melting point of 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole is about a specific temperature range. The determination of the melting point can help to identify the purity of this compound. If the purity is high, the melting point is more acute and the range is narrower; if it contains impurities, the melting point is reduced and the melting range is wider.

Boiling point is also an important physical property. Under specific pressure conditions, when the compound reaches a certain temperature, it changes from liquid to gaseous state, and this temperature is the boiling point. The value of the boiling point can reflect the strength of the intermolecular forces, and it is crucial to know the boiling point for the separation and purification of the compound.

In terms of solubility, this compound behaves differently in different solvents. It may have a certain solubility in organic solvents such as ethanol and dichloromethane, but its solubility in water may be low. This property affects the choice of solvent in the chemical reaction, as well as the separation and purification of the product. If you want to make it participate in the homogeneous reaction, you need to choose its soluble solvent; if you want to separate the product from the reaction system, you can also use a suitable method according to the difference in its solubility.

In summary, the physical properties of 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole play an important role in chemical research, synthesis, application, etc. In-depth understanding of its physical properties can better control the related chemical processes.

What are the chemical properties of 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole

2-Chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole, this is an organic compound. Its chemical properties are unique and have attracted much attention in the field of organic synthesis.

In terms of physical properties, it is mostly solid at room temperature and pressure, but the specific melting point varies depending on the experimental conditions. Generally speaking, the compound has a certain stability, and it may react chemically when exposed to strong oxidants or high temperature environments.

From the perspective of chemical activity, its benzimidazole ring structure gives this compound special reactivity. The nitrogen atom of the benzimidazole ring is rich in lone pairs of electrons and can act as an electron donor to form coordination bonds with metal ions. Therefore, it is widely used in the field of metal-organic chemistry, such as the preparation of metal complexes, which show excellent catalytic performance in catalytic reactions.

Furthermore, the chlorine atom at the 2-position is abnormally active and prone to nucleophilic substitution reactions. Many nucleophiles, such as alcohols and amines, can react with the chlorine atom to form a series of derivatives. This property provides a convenient way to synthesize benzimidazole compounds with diverse structures.

The 1 - [ (4 -fluorophenyl) methyl] fraction, due to the strong electronegativity of fluorine atoms, can have a significant impact on the distribution of molecular electron clouds, thereby changing molecular polarity and chemical reactivity. At the same time, the benzene ring structure also introduces π-π stacking for compounds, which affects their intermolecular interactions in solution or crystal state.

In summary, the chemical properties of 2-chloro-1- [ (4 -fluorophenyl) methyl] -1H-benzimidazole are rich and diverse, and have broad application prospects in many fields such as organic synthesis, materials science and medicinal chemistry.

What is the common synthesis method of 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole?

The common synthesis methods of 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole cover a variety of routes. First, 4-fluorobenzyl chloride and o-phenylenediamine can be used as starting materials. First, dissolve the o-phenylenediamine in an appropriate amount of organic solvent, such as ethanol or dichloromethane, and slowly add 4-fluorobenzyl chloride dropwise at a certain temperature. After the dropwise addition is completed, the temperature is raised and refluxed for several hours to allow the reaction to proceed fully. During the reaction, closely observe the change of the solution, or the formation of precipitation. After the reaction is completed, cool to room temperature, filter, and the resulting solid is washed with an appropriate amount of solvent. After drying, the crude product can be Then purified by means of column chromatography or recrystallization, the target product can be obtained relatively pure.

Second, take o-nitroaniline as the starting material. First, the reduction reaction of o-nitroaniline is carried out to obtain o-phenylenediamine. Commonly used reducing agents include iron powder, sodium sulfide, etc. After the reduction reaction is completed, the separation and purification of o-phenylenediamine are carried out, and then reacted with 4-fluorobenzyl chloride as described above to obtain the target product. In this process, the reduction step requires strict control of the reaction conditions, such as temperature and pH value, to avoid side reactions and affect the purity and yield of the product.

Or other methods can be used, such as the substitution reaction of 2-chloro-1H-benzimidazole with 4-fluorobenzyl halide in the presence of an appropriate catalyst. This reaction requires the selection of suitable catalysts, such as certain metal salts or organic bases, to promote the smooth progress of the reaction. The reaction conditions also need to be finely regulated, such as reaction temperature, time and the proportion of reactants, which all have an important impact on the formation and quality of the product. After synthesis, a purification step is also required to obtain pure 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole.

What are the main application fields of 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole

2-Chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole is useful in various fields.

In the field of medicine, it may be a key intermediate for synthetic drugs. Gain benzimidazole compounds often have a variety of biological activities, such as antibacterial, antiviral, antitumor, etc. 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole After ingenious modification and transformation, new drugs with good curative effect may be created to cure various diseases and eliminate diseases for patients. < Br >
In the field of materials science, it also has its uses. Due to its unique chemical structure, it may participate in the synthesis of polymer materials. Through polymerization and other means, it is integrated into the polymer system to endow the material with different properties, such as enhancing the stability of the material, improving its electrical properties, etc., and then expand the application range of materials, playing an important role in electronic devices, aerospace and other fields.

Furthermore, in the field of agriculture, it also has potential uses. Or it can be used as a starting material for the creation of pesticides to derive compounds with insecticidal, bactericidal or herbicidal effects. Through rational design and research and development, environmentally friendly and efficient agricultural chemicals have been developed to help agricultural harvests, protect crops from pests and diseases, and improve the quality and yield of agricultural products.

In summary, 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole has broad application prospects in many fields such as medicine, materials science, agriculture, etc. It is a very valuable chemical substance. Over time, it will be able to contribute to the development of various industries and benefit the world.

What is the market outlook for 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole?

2-Chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole, this product has considerable market prospects in the current market.

In the field of Guanfu Medicine, many studies are dedicated to exploring the pharmacological properties of this compound. Due to its unique chemical structure, it is expected to emerge in the development of anti-cancer drugs. Cancer cells grow and proliferate in complex mechanisms, and such benzimidazole derivatives may be able to precisely act on key targets to inhibit cancer cells. As far as the market demand for anti-cancer drugs is concerned, the number of cancer patients around the world is increasing day by day, and they are eager for new anti-cancer drugs with high efficiency and low toxicity. If the anti-cancer drugs based on this compound can be successfully developed, the market prospect will be broad, and it will be favored by doctors and patients, and it will win a place in the market.

In the field of pesticides, 2-chloro-1- [ (4-fluorophenyl) methyl] -1H-benzimidazole also has potential application value. It may exhibit outstanding insecticidal and bactericidal activities, escorting agricultural production. Nowadays, people attach great importance to the quality and safety of agricultural products, and the demand for environmentally friendly and efficient pesticides is on the rise. If this compound is in-depth research and development, in line with the concept of green environmental protection, it will be able to conform to the market development trend, win share in the pesticide market, and help the sustainable development of agriculture.

However, the road to market expansion also has challenges. Synthetic process optimization is a top priority, and it is necessary to improve yield and reduce costs in order to enhance market competitiveness. At the same time, strict regulations and long approval processes also add difficulty to the product launch. But overall, 2-chloro-1 - [ (4-fluorophenyl) methyl] -1H-benzimidazole has a bright future in the field of medicine and pesticides. If it can overcome the difficulties, it will be able to shine and reap great results in the market.