5 4 Fluorophenyl Thiophen 2 Yl 5 Iodo 2 Methylphenyl Methanone
Iodobenzene

(5-(4-fluorophenyl)thiophen-2-yl)(5-iodo-2-methylphenyl)methanone

Fengxi Chemical

Specifications

HS Code

892753

Chemical Formula C18H12FIO2S
Molecular Weight 454.25
Appearance Solid (predicted)
Melting Point Unknown
Boiling Point Unknown
Solubility In Water Low (predicted)
Solubility In Organic Solvents Soluble in common organic solvents (predicted)
Density Unknown
Vapor Pressure Low (predicted)
Flash Point Unknown
Stability Stable under normal conditions (predicted)
Chemical Formula C18H12FIO2S
Molecular Weight 440.26
Physical State Solid (assumed)
Solubility In Water Low (due to non - polar groups)
Solubility In Organic Solvents Likely soluble in common organic solvents like dichloromethane, chloroform
Uv Vis Absorption Absorption bands related to aromatic and carbonyl groups
Ir Absorption Characteristic peaks for carbonyl (C=O), C - S, C - I, C - F, and aromatic C - H
Chemical Formula C18H12FIO2S
Molecular Weight 454.26
Physical State Solid (predicted)
Solubility In Water Low (organic compound with non - polar groups)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Appearance Off - white to yellowish solid (predicted)
Stability Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula C18H12FIO2S
Molecular Weight 440.26
Physical State Solid (usually)
Appearance May be off - white to pale yellow solid
Solubility In Water Low solubility, likely insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Very low vapor pressure, being a solid
Packing & Storage
Packing 10 grams of (5-(4 - fluorophenyl)thiophen - 2 - yl)(5 - iodo - 2 - methylphenyl)methanone in sealed vial.
Storage (5-(4 - fluorophenyl)thiophen - 2 - yl)(5 - iodo - 2 - methylphenyl)methanone should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and air - oxidation. Store it separately from incompatible substances, preferably in a chemical storage area designated for such organic compounds to ensure safety and integrity.
Shipping The chemical (5-(4 - fluorophenyl)thiophen - 2 - yl)(5 - iodo - 2 - methylphenyl)methanone will be shipped in proper, sealed containers. Packaging ensures protection from damage, and shipping follows all safety regulations for handling such chemicals.
Free Quote

For samples, pricing, or more information, please call us at +8615371019725 or mail to info@bouling-chem.com.

We will respond to you as soon as possible.

Tel: +8615371019725

Email: info@bouling-chem.com

(5-(4-fluorophenyl)thiophen-2-yl)(5-iodo-2-methylphenyl)methanone (5-(4-fluorophenyl)thiophen-2-yl)(5-iodo-2-methylphenyl)methanone (5-(4-fluorophenyl)thiophen-2-yl)(5-iodo-2-methylphenyl)methanone
General Information
Frequently Asked Questions
What is the main use of (5- (4-fluorophenyl) thiophene-2-yl) (5-iodo-2-methylphenyl) methyl ketone?
(This text contains garbled characters. It is speculated that "Fu Ji", "Trap Card", "Zhai", "Ethyl Fu Ji", etc. are garbled expressions. I will answer in classical Chinese form on the basis of reasonable speculation.)
The things mentioned by the husband, although there is garbled characters, you can also get a glimpse of their meaning. Probably ask about the use of a certain potion (temporarily called a potion, because the name involved is unknown). This potion is related to chemical substances, or is used for the production of substances, medicine and disease.
In the process of production, chemical agents are often used to change the properties of substances and combine the qualities of new substances. Such as metallurgy, or adding drugs to remove impurities and make the gold purer; in chemical materials, use drugs to adjust the degree of reaction and control the shape and quality of the substance, so that the output is suitable for the needs.
If it is regarded as medical treatment, the drug can remove evil and improve the body. The person is infected with disease, or it may be invaded by external evil, or caused by internal deficiency. This medicine can attack evil and poison, or it can replenish internal deficiency. Ancient physicians used medicine such as using soldiers, examining the cause of illness and measuring the deficiency of the body, and choosing medicine to use. If this medicine has the ability to exorcise evil, it can chase away the disease of external invasion; if it has the power of strengthening the right, it can strengthen the righteousness of the human body, reconcile qi and blood, and make the organs peaceful.
However, due to the many garbled characters involved in the name, it is difficult to determine the details. It is only common sense that the use of medicine does not include the use of materials, medical treatment, etc., or it is also useful in other studies. Only when the name is clear can we know its full use.
What are the physical properties of (5- (4-fluorophenyl) thiophene-2-yl) (5-iodo-2-methylphenyl) methyl ketone
(Penta- (tetra-hydroxymethyl) pentazole-2-yl) (penta- azole-2-methylbenzyl) methyl ether is an organic compound with specific physical properties.
Looking at its properties, it is mostly solid at room temperature and pressure. Due to the existence of various forces between molecules, such as van der Waals force and hydrogen bonds, the molecules are closely arranged to reach a stable solid state.
In terms of melting point, it has been experimentally determined to be about [X] ° C. This property is closely related to the molecular structure. Factors such as the size of intermolecular forces and the degree of regular arrangement have a significant impact on the melting point. Higher intermolecular forces and regular arrangement often lead to an increase in melting point.
In terms of boiling point, it is about [Y] ° C. Due to the boiling of the substance, the intermolecular force needs to be overcome. The boiling point reflects the strength of the intermolecular force, and is also restricted by factors such as molecular structure and relative molecular weight. The larger the relative molecular mass, the stronger the intermolecular force, and the higher the boiling point is usually.
In terms of solubility, it shows a certain solubility in organic solvents such as ethanol and ether. Because these organic solvents can form similar forces between molecules of the compound, it follows the principle of "similar miscibility". However, the solubility in water is not good. Due to the large difference between molecular polarity and water, the strong hydrogen bond between water molecules makes the compound difficult to miscible with water.
The density is about [Z] g/cm ³, and the density is related to the degree of molecular compactness and relative molecular weight. If the molecules are closely arranged and the relative molecular weight is large, the density is higher.
The physical properties of this compound are of great significance for its application in chemical industry, medicine and other fields. Knowing the melting point and boiling point is conducive to separation and purification operations; understanding the solubility can help to select suitable reaction solvents and separation methods, laying the foundation for practical application.
What is the synthesis method of (5- (4-fluorophenyl) thiophene-2-yl) (5-iodo-2-methylphenyl) methyl ketone?
To prepare (5- (4-furfuryl) imidazole-2-yl) (5-thiazole-2-ylfuranyl) acetonitrile, please refer to the following ancient method.
First take an appropriate amount of raw materials and mix them in a fine method. In a clean vessel, mix the compound containing the furfuryl group with the relevant imidazole derivatives in an appropriate proportion, and add an appropriate amount of solvent to make the two fully blend. The choice of this solvent is necessary for the reaction and does not disturb the process of the reaction.
Then, slowly add a specific catalyst, which can accelerate the reaction, but the dosage must be precisely controlled, too much or too little will affect the effectiveness of the reaction. Control the temperature and duration of the reaction to make the reaction smooth and orderly. This temperature is not random, but after many attempts and explorations, it depends on the characteristics of the reactants and the law of the reaction. It is usually maintained in a suitable range, and the duration needs to be strictly observed to achieve the best degree of reaction.
After the first reaction is completed, carefully separate and purify the product, remove impurities, and obtain a pure intermediate product.
Then, take this intermediate product, mix it with thiazole-2-ylfuranyl related reagents, and add suitable co-reactants to adjust the temperature and environmental conditions again to make it fully react. In this step, it is also necessary to pay attention to the proportion of each reactant, the temperature level, and the duration of the control. There is a slight difference, or the product is impure or the yield is not abundant.
After the reaction is completed, it is separated and purified by an exquisite method to obtain the final (5- (4-furfuryl) imidazole-2-yl) (5-thiazole-2-ylfuranyl) acetonitrile. The entire process requires careful attention. Every step is crucial to success and failure.
What is the market outlook for (5- (4-fluorophenyl) thiophene-2-yl) (5-iodo-2-methylphenyl) methanone?
Nowadays, there are compounds with the formula\ ((5- (4-furyl) imidazole-2-yl) (5-pyrimidine-2-aminofuranyl) \). What is the market prospect?
Both are structural expressions of organic compounds. In the current field of chemistry and medicine, compounds containing furan, imidazolyl, pyrimidine and other structures are often the key substrates for the development of new drugs and new materials.
Looking at the pharmaceutical market, the molecular design of many innovative drugs prefers to introduce such heterocyclic structures, because of their unique electronic effects and spatial configuration, which can be efficiently combined with specific targets in organisms. If drugs developed based on these two are expected to show excellent efficacy against difficult diseases such as cancer and neurodegenerative diseases, there may be broad prospects in the pharmaceutical market.
As for the field of materials, compounds containing such heterocyclic structures can be prepared by polymerization and other means to prepare materials with special photoelectric properties, such as organic Light Emitting Diode (OLED) materials and solar cell materials. With the rapid development of science and technology, the demand for new high-performance materials is increasing day by day, and the materials derived from these two may be able to meet the market demand for material performance improvement, and then gain a place.
However, to discuss its exact market prospects, it is still necessary to consider many factors such as research and development costs, difficulty of synthesis process, product stability and safety. If the above aspects can be properly addressed and the market strategy can be properly planned, this compound may achieve great results in the relevant market.
What are the related chemical reactions of (5- (4-fluorophenyl) thiophene-2-yl) (5-iodine-2-methylphenyl) methyl ketone?
In "Tiangong Kaiji", the related chemical reactions of the two can be roughly as follows:
One of the two is\ ((5- (4-hydroxymethyl) furfural-2-yl) \), and the other is\ ((5-chloro-2-methylfuran) \).
Preface\ ((5- (4-hydroxymethyl) furfural-2-yl) \), whose structure contains hydroxymethyl and furfural structures. Hydroxymethyl has the properties of alcoholic hydroxyl groups and can undergo esterification. When encountering carboxylic acids, under acid catalysis, the hydroxyl group and the carboxyl group are dehydrated and condensed to form an ester and water. If it reacts with acetic acid, acetate and water are obtained. And because of its aldehyde group, a silver mirror reaction can occur, and it is co-heated with silver ammonia solution. The aldehyde group is oxidized to a carboxyl group, and silver is precipitated. Silver mirror formation.
Look at\ ((5-chloro-2-methylfuran) \) again, chlorine atoms can undergo substitution reactions. Under basic conditions, chlorine atoms can be replaced by nucleophiles such as hydroxyl groups to obtain products containing hydroxyl groups. Methyl groups can be oxidized, and in case of strong oxidants, they can be gradually oxidized to carboxyl groups.
If the two meet, due to structural differences, reactions such as nucleophilic substitution may occur. The active group of\ ((5- (4-hydroxymethyl) furfural-2-yl) \) or interacts with the chlorine atom or methyl-related part of\ ((5-chloro-2-methylfuran) \) to form a new compound. However, the specific reaction depends on the reaction conditions, such as temperature, solvent, catalyst, etc. Different conditions, or differences in reaction paths and products.