Ethane 1 1 Difluoro 2 Iodo
Iodobenzene

Ethane 1 1 Difluoro 2 Iodo

Fengxi Chemical

Specifications

HS Code

531389

Chemical Formula C2H3F2I
Molar Mass 207.947 g/mol
Physical State likely a volatile liquid at room conditions
Melting Point low, consistent with its volatile nature
Density data - specific experimental value needed, but likely less dense than water
Solubility In Water poor solubility, as it is an organic halide
Solubility In Organic Solvents soluble in common organic solvents like hexane, chloroform
Vapor Pressure relatively high due to volatility
Reactivity can undergo substitution reactions due to the presence of iodine atom
Chemical Formula C2H3F2I
Molar Mass 209.945 g/mol
Appearance Unknown
Boiling Point Unknown
Melting Point Unknown
Density Unknown
Solubility In Water Unknown
Vapor Pressure Unknown
Flash Point Unknown
Hazard Class Unknown
Chemical Formula C2H3F2I
Molar Mass 207.946 g/mol
Appearance likely a colorless liquid (estimated from similar haloalkanes)
Solubility In Water low solubility (typical for haloalkanes)
Chemical Formula C2H3F2I
Molar Mass 209.947 g/mol
Physical State Probably a liquid at standard conditions (but needs experimental verification)
Boiling Point Estimated to be relatively low due to its molecular structure and weak intermolecular forces, but exact value unknown without data
Melting Point Unknown without experimental data, likely low
Density Unknown without experimental determination
Solubility In Water Expected to be low as it is an organic halide with non - polar hydrocarbon part
Vapor Pressure Expected to be relatively high due to low molar mass and weak intermolecular forces, but exact value unknown
Reactivity Can undergo substitution reactions due to the presence of iodine as a good leaving group
Packing & Storage
Packing 100 - gram vial packaging for 1,1 - difluoro - 2 - iodo - ethane chemical compound.
Storage 1,1 - Difluoro - 2 - iodo - ethane should be stored in a cool, well - ventilated area away from heat, sparks, and open flames as it may be flammable. Keep it in a tightly closed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents and incompatible substances to prevent chemical reactions. Label the storage container clearly with its name and safety warnings.
Shipping 1,1 - Difluoro - 2 - iodo - ethane is a chemical that may require special shipping precautions due to its potentially hazardous nature. It should be shipped in well - sealed, appropriate containers, following regulations for chemicals, ensuring safety during transit.
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Ethane, 1,1-difluoro-2-iodo- Ethane, 1,1-difluoro-2-iodo- Ethane, 1,1-difluoro-2-iodo-
General Information
Frequently Asked Questions
What are the chemical properties of 1,1-difluoro-2-iodoethane?
1-2,1-diethyl-2-cyanoethyl ketone, which is an important raw material in organic synthesis. Its chemical properties are unique, and due to the specific groups in the structure, it shows a series of special reactivity.
Looking at its structure, the molecule contains key functional groups such as cyano (-CN) and carbonyl (-CO). Cyanyl groups are active and can participate in many reactions such as nucleophilic substitution and addition. For example, under appropriate conditions, cyanyl groups can hydrolyze to form carboxyl groups (-COOH), which is one of the common strategies for constructing carboxylic acid compounds in organic synthesis. Carbonyl is also a reactive activity check point, and can be added to a variety of nucleophiles, such as alcohols, which can form acetal or semi-acetal structures, which is commonly used in protecting carbonyl groups or building complex cyclic structures.
In addition, the α-hydrogen atom in the 1-diethyl-2-cyanoethyl ketone molecule connected to the carbonyl group has a certain acidity due to the double electron-withdrawing effect of the carbonyl group and the cyanyl group. It can be left under the action of a base, which in turn triggers reactions such as hydroxyaldehyde condensation. Through such reactions, carbon chains can be effectively increased to build more complex organic molecular structures. It is widely used in the field of organic synthetic chemistry and has important application value in many disciplines such as pharmaceutical chemistry and materials science.
What are the physical properties of 1,1-difluoro-2-iodoethane?
1%2C1-%E4%BA%8C%E6%B0%9F-2-%E7%A2%98%E4%B9%99%E7%83%B7%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E6%9C%89%E5%93%AA%E4%BA%9B%EF%BC%9F refers to the physical properties of the substance 1,1-dichloroethylene-2-chloroacetonitrile. The following is answered in the classical Chinese format of Tiangong Kaiwu:
1,1-dichloroethylene-2-chloroacetonitrile is mostly in a liquid state at room temperature. Its color may be close to colorless, and it is clear in appearance, but it may also be slightly different due to the preparation method and the existence of impurities. Its smell has a special smell, pungent and disturbing, and uncomfortable when it enters the nose. The cover is also caused by its chemical structure.
In terms of its density, it is larger than water. If it is poured into water, it will sink to the bottom of the water, and the water-liquid will be stratified and determined. As for the boiling point, it is in a specific temperature range. When the external air is pressurized at the standard, it is heated to a certain temperature, and it begins to boil and dissolve gas. This temperature is an important physical characteristic of it, and it is related to its separation and purification.
Furthermore, its solubility is also considerable. In organic solvents, such as ethanol, ether, etc., it is quite compatible, and the miscibility of the two is uniform and indistinguishable from each other. However, in water, its solubility is very small, and when the two meet, they often separate themselves and are difficult to blend.
In addition, 1,1-dichloroethylene-2-chloroacetonitrile is volatile. It gradually gasifies and escapes in the air, and its amount gradually decreases when placed in an open vessel for a long time. This volatilization also makes it easy to spread in the environment, which cannot be ignored.
What is the preparation method of 1,1-difluoro-2-iodoethane?
The formulation method of 1,1-diethyl-2-naphthyl ketone requires multiple fine processes.
Prepare an appropriate amount of naphthalene, acetic anhydride and anhydrous aluminum trichloride first. In a dry and clean reactor with a stirring device and a thermometer, place the naphthalene in an appropriate proportion. Then, under strict temperature control and stirring conditions, slowly add acetic anhydride. This process requires close attention to temperature changes, because the reaction has certain exothermic characteristics.
After the addition of acetic anhydride is completed, maintain stirring for several minutes to make the two initially mix evenly. Next, carefully add anhydrous aluminum trichloride, which is a key catalyst, and its dosage and addition speed have a great impact on the reaction process. When added, the reaction system will change rapidly, and the temperature will also fluctuate. It is necessary to precisely control the reaction temperature within a suitable range with the help of a cooling device to prevent side reactions from occurring.
Continue to stir the reaction at a given temperature for a period of time to allow the reaction to proceed fully. During this period, the reaction system needs to be tested regularly, and the reaction progress and product formation status should be monitored by means such as thin-layer chromatography. When the reaction reaches the expected level, stop stirring, and slowly pour the reaction solution into the pre-prepared ice water containing an appropriate amount of acid for hydrolysis. This step aims to decompose the excess anhydrous aluminum trichloride and unreacted acetic anhydride, and at the same time precipitate the product.
After that, the resulting mixture is separated to collect the organic phase. The organic phase is washed with water and alkali several times to remove impurities, and then dried with desiccants such as anhydrous sodium sulfate. Finally, the dried organic phase is separated and purified by means of distillation to remove low-boiling point and high-boiling point impurities, so as to obtain pure 1,1-diethyl-2-naphthenone.
The whole preparation process requires strict operation at each step, and precise control of temperature, material ratio, reaction time and other factors can produce high-quality products.
In what fields is 1,1-difluoro-2-iodoethane used?
1,1-diethylene-2-cyanopyridinium is useful in various fields. In the field of material chemistry, this compound can be used to prepare materials with specific optoelectronic properties. Due to its unique molecular structure, it can endow materials with excellent fluorescence properties. In the manufacture of organic Light Emitting Diodes (OLEDs), it can be used as a luminescent material to improve the luminous efficiency of the device, improve the color purity, and help its display effect to achieve high quality.
In the field of organic synthesis, 1,1-diethylene-2-cyanopyridinium is often used as a key intermediate. Through a variety of chemical reactions, such as nucleophilic substitution, cyclization reactions, etc., it can be converted into organic compounds with complex structures and unique functions, providing an important cornerstone for the creation of new drugs, pesticides and fine chemicals.
In the field of biomedicine, due to its special chemical properties, it can be modified and used as a biological probe. With its fluorescent properties, it can accurately label and trace specific molecules or cellular structures in organisms, enabling researchers to deeply explore physiological and pathological processes in organisms, and has potential application value in early diagnosis and treatment monitoring of diseases. In addition, in the field of catalysis, after appropriate modification, this compound can be used as a catalyst or ligand to participate in various catalytic reactions, leveraging its unique electronic effect and spatial structure to affect the reaction rate and selectivity, and promote efficient and green catalytic reactions.
What are the storage conditions for 1,1-difluoro-2-iodoethane?
1-2-2-The hidden parts of the shape should be properly placed to avoid the place where the tide is, and to prevent the invasion of the soil, so as to hide them in the place where the earth is dry.
This is an ancient place, and the raw materials are made of gold. It is easy to grow in the case of tide, and its appearance will lose its value. If the soil is tired, it will also be unfavorable for the eyes, and the words and flowers on the wall may be obscured, so as to distinguish.
Furthermore, the place where the earth is dry can be guaranteed not to be contaminated by moisture, and it can also avoid the growth of bacteria, so as to improve its quality. The collection of utensils should be made of wooden cases and boxes, so that they are soft and can be used without colliding with each other and causing grinding.
When taking and placing utensils, also use your hands, or wear gloves, to prevent sweat and oil stains from contaminating the utensils, so that they can be properly hidden, so that the 1-2-2-shaped utensils can keep their ancient appearance for a long time.