1 2 Difluoro 3 Iodobenzene
Iodobenzene

1 2 Difluoro 3 Iodobenzene

Fengxi Chemical

Specifications

HS Code

128668

Chemical Formula C6H3F2I
Molar Mass 254.0
Appearance Liquid (expected, as it's an organic halide with relatively low molecular weight)
Boiling Point Estimated around 170 - 190 °C (based on similar halo - benzene compounds)
Density Estimated around 1.9 - 2.1 g/cm³ (comparable to other halo - benzenes)
Solubility In Water Insoluble (organic halides are generally hydrophobic)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether, and chloroform
Odor Typical aromatic odor (characteristic of benzene derivatives)
Chemical Formula C6H3F2I
Molecular Weight 254.0
Appearance Liquid (usually)
Boiling Point Approx. 193 - 195 °C
Density Data may vary, but around 2.0 - 2.2 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Vapor Pressure Low at room temperature
Chemical Formula C6H3F2I
Molecular Weight 254.0
Appearance Liquid (usually)
Boiling Point Data varies, around 180 - 190 °C
Melting Point Data varies, often low
Density Data varies, higher than water density
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents
Vapor Pressure Low vapor pressure at room temperature
Flash Point Data varies, potentially flammable
Name 1,2 - difluoro - 3 - iodobenzene
Molecular Formula C6H3F2I
Molecular Weight 254.00
Appearance Liquid (usually)
Boiling Point Around 184 - 186 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Cas Number 652-30-2
Chemical Class Haloarene
Chemical Formula C6H3F2I
Molecular Weight 253.99
Appearance Liquid (usually)
Boiling Point Approximately 187 - 189 °C
Solubility In Water Insoluble (organic compound, non - polar)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether, and dichloromethane
Vapor Pressure Low at room temperature
Packing & Storage
Packing 100g of 1,2 - difluoro - 3 - iodobenzene packaged in a sealed, chemical - resistant bottle.
Storage 1,2 - difluoro - 3 - iodobenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. It should be stored in a tightly - sealed container, preferably made of a material that resists corrosion. Avoid storing it near oxidizing agents. Keep the storage area locked if possible, to prevent unauthorized access due to its potentially hazardous nature.
Shipping 1,2 - difluoro - 3 - iodobenzene is shipped in well - sealed, corrosion - resistant containers. Shipment follows strict chemical transport regulations, ensuring proper handling to prevent spills and maintain safety during transit.
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1,2-difluoro-3-iodobenzene 1,2-difluoro-3-iodobenzene 1,2-difluoro-3-iodobenzene
General Information
Frequently Asked Questions
What are the main uses of 1,2-difluoro-3-iodobenzene?
1,2-Diene-3-alkynylbenzene is a key compound in the field of organic synthesis, and its main uses are quite extensive.
In the field of organic synthesis chemistry, one of its important uses is as a key synthesizer. Due to its unique conjugated unsaturated structure, it can participate in many types of chemical reactions, such as cyclization. With appropriate reaction conditions and reagents, 1,2-diene-3-alkynylbenzene can undergo intramolecular cyclization to construct cyclic compounds with complex structures and special properties. This is of great significance for the total synthesis of natural products. The core skeleton of many natural products can be cleverly built by a series of reactions such as cyclization using 1,2-diene-3-alkynylbenzene as the starting material.
In addition, it has also emerged in the field of materials science. Since its unsaturated bonds can polymerize under specific conditions, it can be used to prepare polymer materials with special electrical and optical properties. For example, after careful design and polymerization regulation, the resulting polymers may have good photoelectric conversion properties, and are expected to be applied to optoelectronic devices such as organic solar cells, contributing to the development of new energy materials.
In addition, in terms of medicinal chemistry, 1,2-diene-3-alkynylbenzene may become an important module for the construction of new drug molecules. Its unique structure may endow the constructed drug molecules with special biological activities, and achieve specific binding with targets in vivo, thus opening up new directions for new drug research and development and providing new opportunities for human health. In short, 1,2-diene-3-alkynylbenzene has shown great application potential in many fields such as organic synthesis, materials science and pharmaceutical chemistry due to its unique structure.
What are the physical properties of 1,2-difluoro-3-iodobenzene?
1,2-Diethyl-3-naphthol, its physical properties are as follows:
1,2-diethyl-3-naphthol is mostly a crystalline solid at room temperature, and the quality is more brittle. Looking at its color, it is often white to light yellow. If it is not stored properly, it may be slightly deepened by factors such as light and air oxidation.
Smell it, the substance has a special smell of organic compounds. Although it is not as strong as some pungent substances, it has a unique smell and can be distinguished by close smell.
When it comes to the melting point, it is about a specific temperature range. This is one of the important physical characteristics and can be used for material identification and purity judgment. When heated to the melting point, 1,2-diethyl-3-naphthol gradually melts from a solid state to a liquid state, and the state transition process is clear.
In terms of solubility, 1,2-diethyl-3-naphthol exhibits good solubility in organic solvents such as ethanol and ether, and can be miscible with these solvents in a certain proportion. However, in water, its solubility is very small, and the interaction with water is weak due to the molecular structure of the substance.
In addition, the density of 1,2-diethyl-3-naphthol is also a specific value, which determines its position and distribution in the system when mixed with other substances. And its solid form has a certain response to external conditions such as light and heat. Moderate light or heat may cause subtle changes in physical properties, such as crystal form changes.
What are the synthesis methods of 1,2-difluoro-3-iodobenzene?
There are many synthetic methods for 1% 2C2-diene-3-alkynes. Under the guidance of the spirit of "Tiangong Kaiwu" and the wisdom of the ancients, the common synthetic methods are as follows:
One is the reaction of alkynes and conjugated diolefins. If a suitable alkyne and conjugated diolefins are used as substrates, and under the action of a suitable catalyst, such compounds can be obtained through an addition reaction. This process is like ancient metallurgy, and it is necessary to accurately grasp the ratio of heat and materials. Selecting a suitable catalyst is extremely critical, just as the ancients chose a magic medicine for alchemy, and a suitable catalyst can improve the reaction rate and yield. When the reaction conditions are mild, the purity of the product is quite high, just like the ancient skilled craftsmen creating exquisite utensils, each step requires fine operation.
The second is the reaction between halogenated olefins and alkyne-based metalloreagents. Halogenated olefins are like jade to be carved, and they meet with alkyne-based metalloreagents. In a specific reaction system, the two interact to form a carbon-carbon bond through a substitution reaction, resulting in the formation of 1% 2C2-diene-3-alkyne. This process is like the splicing of tenon and mortise structures, which requires precise docking. The pH, temperature and other factors of the reaction system are like the rules in the hands of craftsmen, and strict control can make the reaction proceed smoothly and produce qualified products.
Third, starting from the starting material containing multi-functional groups, the target structure is constructed through multi-step reactions. This method is similar to painting a large picture. The starting material is the base color of the picture, and each step is like a carefully sketched brush stroke. First, the functional groups of the starting materials are selectively modified, just like a painter selects pigments, carefully. Then through a series of reactions such as elimination, addition, and rearrangement, the unique structure of 1% 2C2-diene-3-alkyne is gradually shaped. This process requires a clear understanding of the reaction mechanism of each step to be able to strategize, just like the ancients wrote books and said, and every word was carefully considered before it could become a masterpiece.
Although the above methods are commonly used in modern chemical synthesis, they all contain the shadow of the wisdom of the ancients. They seem to be inherited from the craftsmanship of "Tiangong Kaiwu". Chemists need to be like ancient craftsmen and strive for excellence in order to make the synthesis go smoothly and obtain ideal products.
What are the precautions for storing and transporting 1,2-difluoro-3-iodobenzene?
1% 2C2-diethylene-3-naphthalene anthracene requires many precautions during storage and transportation.
First, this material may be active in nature. When storing, it must choose a cool, dry and well-ventilated place. Do not place it in a high temperature or humid place to prevent it from deteriorating due to environmental discomfort. High temperature can easily cause its chemical structure to change, and humidity may cause it to react with water vapor, which will damage its quality.
Second, during transportation, protection measures are crucial. It needs to be properly wrapped with suitable packaging materials to ensure that it is not damaged by vibration and collision. The packaging should be strong enough to withstand the bumps and shocks common during transportation, so as to avoid the leakage of 1% 2C2-diethylene-3-naphthalene due to package damage.
Third, because it may be toxic or irritating, whether it is storage or transportation, relevant personnel should be equipped with appropriate protective equipment. If you wear a gas mask to prevent inhalation of its volatile gas, wear protective clothing and protective gloves to avoid skin contact. After operation, you should also clean your body in time to prevent residual substances from endangering your health.
Fourth, the storage and transportation places should be strictly controlled for personnel to enter and exit. Non-relevant professionals are not allowed to enter and exit at will to prevent accidental touch and misuse, resulting in safety accidents. And the place should be equipped with complete emergency treatment equipment and plans. If any leakage or other accident occurs, measures can be taken quickly to reduce the harm.
What is the market price of 1,2-difluoro-3-iodobenzene?
1% 2C2-diene-3-alkynanthracene, the market price situation is quite complicated, and it cannot be hidden by a word. Looking at this genus of alkynanthracene, the change of its price is related to various things.
First, the supply of raw materials. If the raw materials of this alkynanthracene are produced abundantly and supplied smoothly, the price may be stable and flat. However, if the production of raw materials decreases sharply, or the mining encounters obstacles, the supply is not enough, and the price will rise. Such as the ore sources, their mining and smelting conditions, the fluctuation of the price of deep alkynanthracene.
Second, the evolution of technology. If there is a new method for making alkylene anthracene, it can increase production and reduce consumption, so that the amount increases and the cost decreases, and the price may also decrease. The new technology can revolutionize the disadvantages of the old system and make the production smoother. The impact of this on the price should not be underestimated.
Third, the situation of demand. If the demand of alkylene anthracene is prosperous in various industries, such as medicine and electronics, the price will rise due to it. However, the state of the market is impermanent, the change of demand is also fast, the change of fashion, and the ease of use can cause the increase or decrease of demand, and the price will also change accordingly.
Fourth, the regulation of government. The government's government has restrictions on the production, sales, and trade of ethylene anthracene. The severity of taxes and the width and strictness of regulations can disturb its price. Strict regulations and high taxes, or increase the cost, the price will rise; lenient government and tax cuts, or promote its flow, the price may stabilize.
The price of ethylene anthracene in the city is often changing due to raw materials, technology, demand, and politics. Businesses should judge the situation and observe these situations before they can find vitality in the turbulent clouds of the city, control the changes in prices, and make their business.