Methyl 2 Fluoro 5 Iodobenzoate
Iodobenzene

Methyl 2 Fluoro 5 Iodobenzoate

Fengxi Chemical

Specifications

HS Code

983330

Chemical Formula C8H6FIO2
Molar Mass 282.03 g/mol
Appearance Solid (usually)
Physical State At Room Temp Solid
Solubility In Water Low solubility, likely less than 1 g/L due to hydrophobic aromatic and ester groups
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate
Purity Typical purities in commercial products can range from 95% - 99%
Flash Point Estimated to be relatively high, perhaps around 120 - 150 °C based on similar aromatic esters
Chemical Formula C8H6FIO2
Molar Mass 282.03 g/mol
Appearance Solid (likely, based on similar compounds)
Solubility In Water Low (due to non - polar aromatic and ester groups)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Name Methyl 2-fluoro-5-iodobenzoate
Chemical Formula C8H6FIO2
Molar Mass 280.034 g/mol
Appearance Solid (predicted)
Smiles COC(=O)c1cc(F)c(cc1)I
Name Methyl 2-fluoro-5-iodobenzoate
Chemical Formula C8H6FIO2
Molecular Weight 282.034 g/mol
Appearance Typically a solid (physical state may vary based on conditions)
Packing & Storage
Packing 100g of Methyl 2 - fluoro - 5 - iodobenzoate packaged in a sealed glass bottle.
Storage Methyl 2 - fluoro - 5 - iodobenzoate 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 exposure to air and moisture, which could potentially initiate decomposition or reaction. Store it separately from incompatible substances like oxidizing agents and bases.
Shipping Methyl 2 - fluoro - 5 - iodobenzoate is shipped in well - sealed, corrosion - resistant containers. It's transported with strict adherence to chemical safety regulations, ensuring proper handling to prevent leakage and maintain product integrity during transit.
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Methyl 2 Fluoro 5 Iodobenzoate Methyl 2 Fluoro 5 Iodobenzoate Methyl 2 Fluoro 5 Iodobenzoate
General Information
Frequently Asked Questions
What are the main uses of Methyl 2-fluoro-5-iodobenzoate?
Methyl-2-fluoro-5-iodobenzoate is a common raw material for organic synthesis. In the field of organic chemistry, its use is quite extensive.
First, it is often used in the study of medicinal chemistry. With this as a starting material, it can undergo many chemical reactions to build a complex drug molecular structure. Due to the unique electronic and spatial effects of fluorine and iodine atoms in its structure, it can regulate the lipophilicity, metabolic stability and biological activity of drug molecules. After modification and transformation, it can synthesize compounds with specific pharmacological activities to explore new drugs.
Second, it is also used in materials science. Can be used as a precursor to synthesize functional materials. For example, by polymerization or reaction with other compounds, materials with special optical, electrical or thermal properties can be prepared. Because of its specific functional groups, the material can be endowed with unique properties to meet the needs of different fields for material properties.
Third, in the development of organic synthesis methodologies, this compound can be used as a key substrate. Chemists explore new reaction paths and conditions by studying various reactions they participate in, such as nucleophilic substitution, coupling reactions, etc., to promote the progress of organic synthesis chemistry. In conclusion, methyl-2-fluoro-5-iodobenzoate has important uses in drug research and development, material preparation, and organic synthesis methods due to its unique structure and reactivity, providing rich possibilities for research and application in the field of chemistry.
What are the synthetic methods of Methyl 2-fluoro-5-iodobenzoate?
There are various ways to prepare methyl 2-fluoro-5-iodobenzoate. First, it can be obtained from the esterification reaction of 2-fluoro-5-iodobenzoic acid and methanol. In this reaction, concentrated sulfuric acid is often used as a catalyst and stirred at a suitable temperature. First put 2-fluoro-5-iodobenzoic acid in a reaction vessel, add an appropriate amount of methanol, then slowly add the catalyst dropwise, heat it to a certain temperature, such as 60-80 ° C, and pay close attention to the reaction process during the reaction. After the reaction is completed, the pure product is obtained by conventional separation and purification methods, such as extraction, distillation, etc.
Second, it can be started from 2-fluorobenzoic acid. First, 2-fluorobenzoic acid and iodine substitutes, such as iodine elemental substance, potassium iodide, etc., undergo iodization reaction under specific conditions, and introduce iodine atoms at the 5-position of the benzene ring to obtain 2-fluoro-5-iodobenzoic acid. Then, the esterification reaction with methanol as described above is carried out to achieve the synthesis of the target product. In this path, the conditions of the iodization reaction are quite critical, and factors such as reaction solvent, catalyst, temperature, etc., all affect the yield and selectivity of the reaction.
Or, use methyl benzoate as the starting material. First, the benzene ring of methyl benzoate is fluorinated to introduce fluorine atoms to form methyl 2-fluorobenzoate. After that, the iodization reaction is carried out, and the iodine atom is introduced at the 5-position to obtain methyl 2-fluoro-5-iodobenzoate. This synthesis route and the control of the reaction conditions at each step play a crucial role in the success or failure of the overall synthesis and the yield. After each step of the reaction, proper separation and purification are required to ensure the smooth progress of the next reaction.
What are the physical properties of Methyl 2-fluoro-5-iodobenzoate?
Methyl 2-fluoro-5-iodobenzoate is one of the organic compounds. Its physical properties are well-researched.
Looking at its properties, under normal temperature and pressure, it is mostly a colorless to light yellow liquid, or a crystalline solid. This varies depending on the preparation process and the environment. Its melting point and boiling point are the key physical quantities for identifying this compound. The melting point is covered by a specific temperature range, about [X] ° C. At this temperature, the substance gradually melts from the solid state to the liquid state. The boiling point, under a certain pressure environment, is about [X] ° C. The substance changes from liquid state to gaseous state.
As for the density, it is also an important physical property. Its density is about [X] g/cm ³, which is related to the stratification condition and the amount of space it occupies when mixed with other substances.
In terms of solubility, methyl 2-fluoro-5-iodobenzoate exhibits good solubility in organic solvents such as ethanol, ether, dichloromethane, etc. Due to the principle of "similar miscibility", its molecular structure is similar to that of organic solvents, so it can be miscible with each other. However, in water, its solubility is very small, because its molecular polarity is quite different from that of water, it is difficult to form an effective interaction.
Furthermore, the refractive index of this compound also has its specific value, which is about [X]. The refractive index reflects the degree of refraction of light when it propagates in it, and can be used for purity identification and characterization of material properties.
In summary, the physical properties of methyl 2-fluoro-5-iodobenzoate, such as properties, melting point, boiling point, density, solubility, and refractive index, are of indispensable significance in many fields such as chemical research, chemical production, and quality inspection, laying the foundation for in-depth exploration of its chemical behavior and applications.
What are the chemical properties of Methyl 2-fluoro-5-iodobenzoate?
Methyl-2-fluoro-5-iodobenzoate, this is an organic compound. Its chemical properties are very interesting, let me go into detail.
First of all, in its molecular structure, the benzoate part gives it a certain stability. The ester group (-COOCH) is relatively mild in nature and can remain stable under common conditions. However, in the environment of strong acid or strong base, the ester group is easy to hydrolyze. In the case of strong acid, the hydrolysis produces benzoic acid and methanol. This reaction is reversible. When the concentration and temperature of the acid in the environment change, the reaction equilibrium will also change. In the case of strong base, the hydrolysis is more thorough, and carboxylate and methanol are formed, which is an irreversible reaction.
Furthermore, the introduction of fluorine atoms brings unique properties to the molecule. Fluorine atoms have extremely high electronegativity, resulting in increased molecular polarity. This not only affects its physical properties, such as solubility, but also increases solubility in polar solvents; in chemical reactions, fluorine atoms have a significant impact on the density of ortho and para-electron clouds, which changes the activity of electrophilic substitution reactions on the benzene ring. Usually, the density of ortho and para-electron clouds decreases, and the difficulty of attacking electrophilic reagents increases.
Iodine atoms, on the other hand, have a large atomic radius and strong polarizability. In some reactions, iodine atoms are easy to leave and participate in nucleophilic substitution reactions as leaving groups. For example, when reacting with nucleophiles, iodine atoms can be replaced by nucleophilic reagents to generate new organic compounds. At the same time, the presence of iodine atoms also affects the spatial structure of the molecule, which in turn affects the intermolecular forces and physical properties.
Methyl-2-fluoro-5-iodobenzoate has rich and diverse chemical properties, and its ester group, fluorine atom and iodine atom interact, resulting in its unique reactivity and physical properties. It has a wide range of application prospects in the field of organic synthesis.
What is the price range of Methyl 2-fluoro-5-iodobenzoate in the market?
If you want to know the price range of Guanfu methyl 2-fluoro-5-iodobenzoate, it is difficult to confirm the price range. However, it can be speculated based on past business examples and changes in the prices of related things.
The price of Fu chemical industry often changes due to various factors. The rarity of its raw materials, if the raw materials for making this ester are scarce and rare, the price will be high; if the raw materials are abundant and easy to extract, the price may be slightly flat. And the difficulty of preparation is also important. If the preparation method is complicated, exquisite equipment and precious reagents are required, and the cost will be high, and the price will follow.
Furthermore, the influence of supply and demand is particularly severe. If there is a strong demand for methyl 2-fluoro-5-iodobenzoate in the market, and the output is limited, the price will rise; if there is little demand and excess output, the price may decline.
In the past, the price of this kind of fine chemical products with high quality and excellent purity may be between tens and hundreds of yuan per gram. If it is for industrial use, the purity is slightly inferior, and the quantity is large, the price per kilogram may be in the range of thousands of yuan. However, this is only speculation, and the actual price may vary greatly depending on time, place, and market conditions. To obtain an accurate price, it is also necessary to inquire from firms and merchants specializing in chemical materials, or check recent business records to obtain the exact number.