1 Difluoromethoxy 4 Iodobenzene
Iodobenzene

1 Difluoromethoxy 4 Iodobenzene

Fengxi Chemical

Specifications

HS Code

120966

Chemical Formula C7H5F2IO
Molecular Weight 284.014
Appearance Typically a colorless to light - colored liquid or solid (description may vary based on purity and conditions)
Boiling Point Data may vary; estimated based on similar compounds around 200 - 250°C under normal pressure (approximate, needs experimental verification)
Melting Point No common value found, prediction based on structure might suggest a relatively low melting point, perhaps around - 20 to 20°C (approximate, needs experimental verification)
Density Estimated around 1.9 - 2.1 g/cm³ (approximate, based on related halogen - containing aromatic compounds)
Solubility In Water Insoluble in water due to non - polar aromatic and fluorinated groups
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate, etc., due to its organic nature
Vapor Pressure Low vapor pressure at room temperature as it is an aromatic halogen - containing compound
Stability Stable under normal conditions; may be reactive under extreme conditions or in the presence of strong oxidizing or reducing agents
Chemical Formula C7H5F2IO
Molecular Weight 270.01
Appearance Solid (Typical)
Solubility In Water Low (due to non - polar nature of benzene ring)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Low at room temperature (Estimated based on similar structures)
Stability Stable under normal conditions but can react with strong oxidizing agents
Chemical Formula C7H5F2IO
Molecular Weight 284.015
Appearance Typically a colorless to light - yellow liquid
Boiling Point Data may vary, around 200 - 220 °C under normal pressure (estimated)
Density Estimated to be around 1.9 - 2.1 g/cm³ (organic iodide and fluorine - containing compound density range)
Solubility Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate
Vapor Pressure Low vapor pressure at room temperature, volatile under heating
Flash Point Caution in handling due to flammability, flash point likely above 60 °C (estimated)
Stability Stable under normal conditions, but sensitive to strong oxidizing agents
Chemical Formula C7H5F2IO
Molecular Weight 272.01
Appearance Solid (Typical)
Solubility In Water Low (Organic compound, non - polar nature)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, toluene
Vapor Pressure Low (Based on its solid - like nature at room temperature)
Stability Stable under normal conditions, avoid strong oxidizing agents
Packing & Storage
Packing 100g of 1-(difluoromethoxy)-4-iodobenzene packaged in a sealed, labeled bottle.
Storage 1-(Difluoromethoxy)-4-iodobenzene should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. Keep it in a tightly sealed container to prevent evaporation and exposure to air and moisture, which could potentially lead to degradation. Store it separately from incompatible substances, like oxidizing agents, to avoid chemical reactions.
Shipping 1-(Difluoromethoxy)-4-iodobenzene is shipped in accordance with strict chemical transport regulations. It's carefully packaged in suitable containers to prevent leakage, with documentation noting its properties for safe and compliant shipping.
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1-(difluoromethoxy)-4-iodobenzene 1-(difluoromethoxy)-4-iodobenzene 1-(difluoromethoxy)-4-iodobenzene
General Information
Frequently Asked Questions
What is the main use of 1- (difluoromethoxy) -4-iodobenzene?
Diethylaminoethyl-4-chlorobenzoate, its main uses are as follows:
This substance is used in the field of medicine and is often used as a local anesthetic. It plays an important role in minor surgical operations, dermatological treatment and other scenes. For example, when superficial skin surgery is performed, it is applied to the surgical site in an appropriate amount, which can block the conduction of nerve impulses and produce an anesthetic effect in the area, so that the patient does not feel pain during the operation, greatly relieving the pain of the patient, and creating favorable conditions for the doctor to carry out the operation smoothly.
In some special experimental scenarios, due to its anesthetic properties, it will also be used to perform local anesthesia on specific parts of experimental animals, so that researchers can perform various experimental operations and observations while the animals remain relatively quiet and painless, to ensure the accuracy of experimental data and the smooth progress of the experimental process.
At the same time, in some clinical diagnostic operations, such as gastroscopy, colonoscopy and other invasive operations, appropriate use of it can effectively reduce patient discomfort, improve patient tolerance, and help the diagnostic process proceed smoothly.
In addition, in the process of some drug development, as an ingredient with local anesthetic activity, it may also be used to construct new pharmaceutical dosage forms or compound formulations to meet the treatment needs of different diseases and the requirements of administration methods.
What are the physical properties of 1- (difluoromethoxy) -4-iodobenzene?
The physical properties of dichloroacetyl-4-azofur are as follows:
This substance is often in a specific form, or in a solid state, its texture may be solid and dense, and it has a certain stability at room temperature and pressure. Looking at its color, it is either pure and white, or slightly yellowish, like light dyeing in the early morning sun, with uniform and pure color, just like a naturally carved jade.
Its smell, if you smell it carefully, may have a hint of elegant but unique smell, not pungent and unpleasant, nor fragrant, just like invisibly revealing its uniqueness.
When it comes to solubility, in some common organic solvents, such as alcohols and ethers, they may exhibit good solubility characteristics, just like ice and snow merging into spring streams, quietly melting, regardless of each other. However, in water, its solubility may be relatively limited, such as Ping on water, which is difficult to completely melt.
Its melting point is also one of the important physical properties. At a specific temperature, it is like melting ice and snow, gradually transforming from solid to liquid. This temperature is like a key node in its physical transformation, which is precise and unique.
Furthermore, its density may be similar to that of common similar substances. When weighing, one can feel the specific relationship between its mass and volume. Although it is not as heavy or as light as a feather, it shows its unique ratio of mass to volume within a specific range.
Dichloroacetyl-4-zolfur has different applications and characteristics in many fields due to its unique physical properties, waiting for the world to further explore and discover.
Is the chemical property of 1- (difluoromethoxy) -4-iodobenzene stable?
The chemical properties of 1-% (diethylamino) -4-azoquinoline are quite stable. Both contain special chemical structures, which endow them with unique properties.
Let's talk about 1- (diethylamino) first, the amino group connected to the ethyl group, which has a certain electron supply effect. Amino nitrogen atoms have lone pair electrons, which can participate in the adjustment of electron cloud distribution and can affect the electron cloud density of surrounding atoms. Due to the amino power supply, the electron cloud density of the connected part increases. In chemical reactions, this part is more likely to attract electrophilic reagents to attack, thus exhibiting active nucleophilicity. However, the existence of diethyl groups enhances the density of the amino electron cloud due to the push electron effect of alkyl groups, and at the same time increases the steric resistance. The steric hindrance effect will prevent some reagents from getting close to the amino group, so that the reactivity changes under specific circumstances, and the stability of the system is maintained to some extent.
Besides 4-azido quinoline, the azido group is a highly active group, but it can maintain a certain stability in the quinoline system. Quinoline is a nitrogen-containing heterocyclic aromatic hydrocarbon, and its conjugate system is huge. The azido group is connected to the fourth position of the quinoline ring and will interact with the quinoline ring conjugate system. Electrons are delocalized in the entire conjugate system, so that the energy of the azido group is dispersed, and it is not easy to decompose violently like the free azido group. The spatial structure of the quinoline ring also protects the azide group, and the distribution of surrounding atoms and groups limits the contact between external reagents and azide groups, further enhancing the stability. However, it should be noted that although its stability is relatively high, in case of high temperature, strong impact or specific catalytic conditions, azide groups may still release nitrogen to decompose and initiate chemical reactions.
What are the synthesis methods of 1- (difluoromethoxy) -4-iodobenzene?
The synthesis of 1 - (diethylamino) - 4 - bromonaphthalene is an important topic in the field of chemical synthesis. To obtain this compound, there are many common methods.
First, the naphthalene can be started from the naphthalene. First, the naphthalene is brominated, and a suitable brominating reagent, such as liquid bromine and a suitable catalyst, is introduced into a specific position in the naphthalene ring at a suitable temperature and reaction conditions to obtain 4 - bromonaphthalene. Subsequently, 4 - bromonaphthalene is nucleophilically substituted with diethylamine. With the assistance of basic conditions, such as potassium carbonate and other bases, the reaction occurs smoothly, and finally 1 - (diethylamino) - 4 - bromonaphthalene is obtained. The advantage of this route is that the raw material naphthalene has a wide range of sources, the price is relatively low, and the reaction conditions of each step are relatively easy to control. However, the nucleophilic substitution step or the existence of side reactions requires fine regulation of the reaction conditions to improve the yield.
Second, the compound containing diethylamino is reacted with the precursor containing the brominated naphthalene structure. For example, a reagent containing diethylamino group and a suitable active group can be prepared first, and a compound with bromine atom introduced at a specific position in the naphthalene ring can be synthesized through a specific organic reaction, such as the Ullman reaction, in the presence of metal catalysts and ligands, to achieve the formation of carbon-nitrogen bonds, thereby synthesizing the target product. The advantage of this method is that it can accurately construct the structure of the target molecule, and there are relatively few side reactions. However, the cost of metal catalysts and ligands is higher, the reaction conditions are more demanding, and the reaction equipment and operation requirements are higher.
Another method can be synthesized by multi-step series reaction or one-pot method from the perspective of molecular design. First, the reactants are rationally designed, so that multiple reactions can occur in sequence in the same reaction system, reducing the separation steps of intermediates, and improving atomic economy and reaction efficiency. However, such methods require extremely high requirements for understanding the reaction mechanism and controlling the reaction conditions, and require in-depth research and exploration before they can be successfully realized.
What is the price range of 1- (difluoromethoxy) -4-iodobenzene in the market?
Today there is dihydroxyethylaminopropylamine-4-imidazole, what is the market price? This question is quite difficult, because the market situation is changeable, and the price is also changeable. However, you can try it with common sense.
Dihydroxyethylaminopropylamine-4-imidazole is also a chemical product. The price of its price is related to the number. First, the price of raw materials. If the raw materials are easily available and cheap, the price of the finished product may not be high; on the contrary, if the raw materials are rare and expensive, the price will increase. Second, the simplicity of the process. The more complex the craft, the more manpower and material resources are required, and the price will rise; if the craft is simple, the price may drop slightly. Third, the supply and demand of the market. If there are many applicants and few suppliers, the price will rise; if the supply exceeds the demand, the price will fall.
Looking at the current market conditions, if the quality is average, the supply is sufficient, and the cost of raw materials is not very high, the price per gram may be between tens and one or two hundred. However, if the quality is high, or it is used for special purposes, the requirements for purity are strict, and the raw materials are rare and the craftsmanship is complex, the price per gram may reach hundreds or even higher.
To be clear, this is only a guess, and the actual price shall be subject to the current market. The price sold by merchants may vary due to profit. To know the exact price, you must enter the market in person and ask the store owner before you can get it.