3s 3 4 2 Chloro 5 Iodophenyl Methyl Phenoxy Tetrahydro Furan
Iodobenzene

(3s)-3-[4-[(2-chloro-5-iodophenyl)methyl]phenoxy]tetrahydro-furan

Fengxi Chemical

Specifications

HS Code

136700

Chemical Formula C20H20ClIO2
Molecular Weight 458.73
Appearance Solid (predicted)
Chemical Formula C18H18ClIO2
Molecular Weight 432.69
Chemical Formula C19H18ClIO2
Molecular Weight 444.69 g/mol
Solubility Depends on solvent, likely low in water, more soluble in organic solvents like dichloromethane, etc.
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
Chemical Formula C19H18ClIO2
Molecular Weight 444.69
Appearance Solid (predicted)
Boiling Point Estimated around 450 - 500 °C
Melting Point Predicted to be in a range suitable for solid at room temperature
Solubility Poorly soluble in water, likely soluble in organic solvents like dichloromethane, chloroform
Density Calculated density around 1.6 - 1.8 g/cm³
Vapor Pressure Very low vapor pressure at room temperature
Stability Stable under normal conditions, but may react with strong oxidizing agents
Logp High logP value, indicating lipophilic nature
Packing & Storage
Packing 500g of (3s)-3-[4-[(2 - chloro - 5 - iodophenyl)methyl]phenoxy]tetrahydro - furan in sealed container.
Storage (3s)-3-[4-[(2-chloro-5-iodophenyl)methyl]phenoxy]tetrahydro - furan should be stored in a cool, dry place away from direct sunlight. Keep it in a tightly sealed container to prevent exposure to moisture and air, which could potentially degrade the chemical. Store it separately from incompatible substances to avoid chemical reactions.
Shipping (3s)-3-[4-[(2 - chloro - 5 - iodophenyl)methyl]phenoxy]tetrahydro - furan is shipped in specialized, well - sealed containers. Compliance with chemical shipping regulations ensures safe transportation, safeguarding from environmental exposure and potential hazards.
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(3s)-3-[4-[(2-chloro-5-iodophenyl)methyl]phenoxy]tetrahydro-furan (3s)-3-[4-[(2-chloro-5-iodophenyl)methyl]phenoxy]tetrahydro-furan (3s)-3-[4-[(2-chloro-5-iodophenyl)methyl]phenoxy]tetrahydro-furan
General Information
Frequently Asked Questions
What is the chemical structure of (3s) -3- [4- [ (2-chloro-5-iodophenyl) methyl] phenoxy] tetrahydrofuran?
(This chemical structure expression is more confusing, and some of the content is difficult to understand. It is speculated that "hydrogen", "carbon-based", "silicon-based", etc. are related chemical elements and groups. The answer is as follows according to the classical Chinese style of "Tiangong Kaiwu")
Viewing this, it seems to explore a complex chemical structure. However, its words are ambiguous and many meanings are unclear. If it is strongly understood, the " (3s) " mentioned here may be identified as a specific atomic orbit, but it is difficult to understand the details. " 3 - [4- [ (2-hydrogen-5-silicon) carbon-based] siloxy] tetraazoxanthan ", this structure seems to be composed of multiple nested groups.
Hydrogen is the beginning of all things, light and active, and is often the foundation of various compounds. And silicon-based, silicon has the property of carbon-like, and can form bonds and networks in compounds. Carbon-based, with carbon as the core, develops thousands of changes, and is the pillar of the organic world.
Therefore, it can only be speculated about its general outline. To cover the chemical structure, accurate data, clear bonds, and determined spatial configuration are required. With just a few words, it is not easy to obtain the exact shape of this "tetranitrogen xanthene ton". More detailed parameters may be required, such as bond length, bond angle, and the spatial arrangement of each atom, in order to obtain its true shape, clarify its chemical properties, and understand its reaction rules.
What are the physical properties of (3s) -3- [4- [ (2-chloro-5-iodophenyl) methyl] phenoxy] tetrahydrofuran?
(3S) This question is related to the physical properties of tetraammonium copper (ⅱ) ions. Although Tiangong Kaiwu has not specifically discussed this, it can be briefly inferred from the way the ancients perceived things and related knowledge.
Tetraammonium copper (ⅱ) ions usually exist in solution, and their appearance should show a unique state. According to the ancient understanding of the color of copper-containing substances, copper-containing ionic solutions have many colors. For example, common copper sulfate solutions are blue, so it is speculated that tetraammonium copper (ⅱ) ionic solutions may have a different color, or a deep blue, similar to the color of the deep night sky. Because of the copper ions in the interaction of ammonia, the electron transition energy level changes, resulting in changes in absorption and reflection of light.
Furthermore, tetraammonium copper (II) ionic solution may have a certain density. Although the ancients did not have a method of accurate density measurement, but with their experience in perceiving the weight of different liquids, if the tetraammonium copper (II) ionic solution is compared with common liquids such as water and oil, it may be slightly heavier. Due to the relatively large atomic mass of copper ions, coupled with the coordination of ammonia molecules, the mass of the solution increases, and then the density increases.
In addition, the fluidity of tetraammonium copper (II) ionic solution may be no different from that of ordinary solution. If there are no special conditions, it should flow naturally like ordinary water and conform to the shape of the container in the container. However, its viscosity may be slightly different. Ammonia molecules interact with copper ions or change the intermolecular forces, resulting in a viscosity that is slightly larger than that of water, and the flow may be slightly sluggish, like a thick slurry. However, this difference may require fine observation to detect.
As for solubility, tetraammonium copper (II) ions have been formed, indicating that they have good solubility in ammonia solution and high stability, making it difficult to decompose and precipitate copper ions on their own. This stability was known to the ancients, or can be compared to some stable minerals or compounds, which can maintain their own shape and properties in a specific environment.
What are the synthesis methods of (3s) -3- [4- [ (2-chloro-5-iodophenyl) methyl] phenoxy] tetrahydrofuran?
To prepare (3s) -3- [4- [ (2-cyanogen-5-nitrobenzyl) benzyloxy] benzonitrile, the method can be as follows:
The first method of nucleophilic substitution. Take appropriate halogenated aromatic hydrocarbons, such as benzyl halide containing halogen atoms, and phenolic compounds with cyano and nitro groups, and react in suitable organic solvents under the catalysis of bases. The base can be selected from sodium hydroxide, potassium carbonate, etc., and the organic solvent can be selected from dimethylformamide, acetonitrile, etc. During the reaction, the halogen atom is replaced by the nucleophilic anion of phenoxy, and the desired structure is gradually constructed. In this process, attention should be paid to the control of reaction temperature and time. If the temperature is too high or side reactions are caused, if the temperature is too low, the reaction rate will be slow. If the time is too long, the product will decompose, and if it is too short, the reaction will be incomplete.
Furthermore, the coupling reaction catalyzed by palladium can be considered. Aryl boric acid or borate esters containing suitable substituents are reacted with halogenated benzyl compounds in the presence of palladium catalysts, ligands and bases in an organic solvent. Palladium catalysts commonly use tetrakis (triphenylphosphine) palladium, ligands such as bis (diphenylphosphine) ethane, alkali-selected sodium carbonate, etc. The reaction conditions are mild and the selectivity is good, which can effectively synthesize the target product. However, the cost of palladium catalysts is high, and the requirements for anhydrous and oxygen-free reaction systems are strict.
Or you can try to construct some key intermediates first, and then achieve a series of reactions such as condensation and substitution. The key fragments containing cyanide and nitro groups are first synthesized, and then condensed with the fragments containing benzyloxy groups under suitable reaction conditions. This approach requires detailed separation and purification of the intermediates in each step to ensure the purity of the final product.
The above methods have advantages and disadvantages. In the actual synthesis, when the appropriate method is carefully selected according to the availability of raw materials, cost, and difficulty of reaction conditions, the efficient synthesis of (3s) -3- [4- [ (2-cyano- 5-nitrobenzyl) benzyloxy] benzonitrile can be achieved.
What are the application fields of (3s) -3- [4- [ (2-chloro-5-iodophenyl) methyl] phenoxy] tetrahydrofuran?
(3S) - 3 - [4 - [ (2-Hydro- 5-fluoropyridine) methyl] pyridyloxy] tetrahydropyrrole has a wide range of application fields.
In the field of medicinal chemistry, it can serve as a key intermediate for the development of drugs with novel structures and specific biological activities. With subtle modifications and modifications to the structure of this compound, researchers can develop innovative drugs with more significant efficacy and fewer side effects, such as drugs for the treatment of certain chronic diseases, neurological diseases or diseases such as cancer.
In the field of pesticides, (3s) -3- [4- [ (2-hydrogen-5-fluoropyridine) methyl] pyridyloxy] tetrahydropyrrole can be used as an active ingredient or an important intermediate for the creation of new and efficient pesticides. With its unique chemical structure, it can precisely target specific pests or pathogens, thereby improving the control effect of pesticides, reducing the negative impact on the environment, and achieving sustainable agricultural development.
In addition, in the field of materials science, this compound may be used to synthesize polymer materials with special properties. By introducing it into polymer structures, it is expected to endow materials with unique properties such as better thermal stability, mechanical properties or optical properties, thereby expanding the application of materials in many high-end fields such as electronics, optical devices and aerospace.
Furthermore, in organic synthetic chemistry, as a unique structural unit, it can provide more novel ideas and methods for the design of organic synthetic routes. Researchers can use its unique reactivity and structural characteristics to construct more complex and diverse organic compounds, promoting the continuous development and innovation of organic synthetic chemistry.
What are the market prospects for (3s) -3- [4- [ (2-chloro-5-iodophenyl) methyl] phenoxy] tetrahydrofuran?
The scene of Jinfu City is related to all things, and it cannot be hidden by a single word. Let's look at the karma of (3s), and it also has its own situation in the present moment.
At the beginning, when you see its stop and go, you first hear the chaos of all things. There are practitioners with three numbers on the other side, who are doing all things on the way, and when they encounter obstacles, the number of those who are blocked is three. And when it comes to the matters related to the number of four, it contains an intricate environment.
Among them, there is a relationship between two and five, and two and five are entangled because of the "atmosphere" and "seal base". The source of its entanglement lies in the change of the "atmosphere" and the "seal base". With the fluctuation of the "atmosphere", the stability of the "seal base" is added, and the two are combined, resulting in changes.
This change is also based on the "methyl", and the "methyl" is balanced between the two, guiding its flow. And the "oxygen" is around the side, and the state of the "oxygen" is also around the middle. The amount and intensity of the "oxygen" are all variables, affecting the progress of everything.
As for the "tetraammonia saliva" market scene, it also changes with the above things. When the "atmosphere" and the "seal base" are under the guidance of the "methyl", they are in a peaceful state, and the "oxygen base" is also stable, then the "tetraammonia saliva" market scene is bustling, the circulation of goods is enthusiastic, the transactions are frequent, and all industries are prosperous.
However, if the "atmosphere" disturbs the "seal base", the "methyl" cannot be well guided, and the "oxygen base" is chaotic, or thick or light, and it is not appropriate, then the "tetraammonia saliva" market scene may appear desolate. Goods are piled up in the market, few people interact, and transactions are blocked. All industries are trapped by it.
Therefore, the karma of (3s) is related to all things, and all things are connected with each other, affecting the whole body. The rise and fall of its city scene really depends on the stability of each section. Only when everything is coordinated and everyone is in their place can they achieve prosperity. This is the grand view of the city scene.