5 Fluoro 3 Iodo Benzoic Acid
Iodobenzene

5 Fluoro 3 Iodo Benzoic Acid

Fengxi Chemical

Specifications

HS Code

752544

Name 5-fluoro-3-iodo-benzoic Acid
Chemical Formula C7H4FIO2
Molar Mass 266.01 g/mol
Appearance Solid (likely white or off - white powder)
Solubility In Water Low solubility, as it is an aromatic carboxylic acid with non - polar groups
Melting Point Typically in the range where organic aromatic acids melt (specific value would require experimental determination)
Pka Carboxylic acid group has a pKa characteristic of benzoic acid derivatives (around 4 - 5 range)
Reactivity Reactive at the carboxylic acid group (e.g., can form esters, amides) and at the aromatic ring (electrophilic substitution due to presence of halogen and fluorine)
Chemical Formula C7H4FIO2
Molar Mass 284.01 g/mol
Appearance Solid (likely white or off - white powder)
Physical State At Room Temperature Solid
Solubility In Water Low (organic acid with fluorine and iodine substituents)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Melting Point Data - specific value needed (expected to be in a certain range for aromatic carboxylic acids)
Boiling Point Decomposes before boiling (common for many organic acids with halogen substituents)
Acidity Pka Value related to aromatic carboxylic acid with electron - withdrawing groups
Density Data - specific value needed (estimated based on similar compounds)
Chemical Formula C7H4FIO2
Molar Mass 270.01 g/mol
Appearance Solid
Color White to off - white
Solubility In Water Low
Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane
Melting Point 153 - 157 °C
Boiling Point Decomposes before boiling
Pka Around 3 - 4 (acidic nature)
Stability Stable under normal conditions, but sensitive to light and heat
Chemical Formula C7H4FIO2
Molar Mass 284.01 g/mol
Appearance Solid (usually a white to off - white powder)
Solubility In Water Poorly soluble
Solubility In Organic Solvents Soluble in some organic solvents like dichloromethane, chloroform
Melting Point Typically in a certain range (needs more specific data)
Pka Value Characteristic acidic dissociation constant (specific value needs more research)
Density Needs experimental determination for accurate value
Stability Stable under normal conditions, but light - sensitive
Packing & Storage
Packing 5 - fluoro - 3 - iodo - benzoic Acid: 100g packed in a sealed, chemical - resistant plastic bottle.
Storage 5 - Fluoro - 3 - iodo - benzoic acid should be stored in a cool, dry place away from heat sources and direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and potential reactions with air components. Store it separately from incompatible substances, such as strong oxidizing agents and bases, to avoid chemical degradation.
Shipping 5 - fluoro - 3 - iodo - benzoic acid is shipped in well - sealed, corrosion - resistant containers. Shipment follows strict chemical transport regulations, ensuring proper handling to prevent leakage and maintain the integrity of this potentially hazardous chemical.
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5-fluoro-3-iodo-benzoic Acid 5-fluoro-3-iodo-benzoic Acid 5-fluoro-3-iodo-benzoic Acid
General Information
Frequently Asked Questions
What are the chemical properties of 5-fluoro-3-iodo-benzoic Acid?
5-Fluoro-3-iodobenzoic acid is one of the organic compounds. In its molecular structure, above the benzene ring, the fluorine atom occupies the 5th position, the iodine atom is at the 3rd position, and there are benzoic acid groups connected. This compound has a variety of chemical properties, let me tell you one by one.
First of all, its acidity is significant. Benzoic acid is already acidic, and the substitution of fluorine and iodine is due to the high electronegativity of the two. Through the induction effect, the density of the carboxyl group electron cloud is reduced, and the acidity is even more acidic than that of benzoic acid. In chemical reactions, this acidic property often causes it to neutralize with bases and generate corresponding salts.
Furthermore, its halogen atoms are active. The fluorine and iodine atoms in 5-fluoro-3-iodobenzoic acid can participate in many nucleophilic substitution reactions due to the characteristics of halogen atoms. Although the fluorine atom has a large carbon-fluorine bond energy and is difficult to replace, it can still be replaced by nucleophilic reagents under specific conditions. The carbon-iodine bond attached to the iodine atom is relatively weak, and it is easier to be attacked by nucleophilic reagents. Common nucleophilic reagents such as alkoxides and amines can react with it to form new carbon-heteroatomic bond compounds.
In addition, the conjugate system of the benzene ring endows it with certain stability and electron delocalization. This stability makes the compound relatively stable under general conditions. However, due to the electron cloud distribution of the benzene ring, electrophilic substitution reactions can occur. Although fluorine and iodine on the benzene ring are ortho-and para-localizers, although blunt benzene rings are caused, electrophilic reagents can still selectively attack their ortho-and para-sites, and various benzene ring substitution products can be derived.
In the field of organic synthesis, 5-fluoro-3-iodobenzoic acid has a wide range of uses. It can be used as an intermediate to construct complex organic molecular structures through the above substitution reactions, which can be used in the creation of fine chemicals such as medicine and pesticides.
What are the main uses of 5-fluoro-3-iodo-benzoic Acid?
5-Fluoro-3-iodobenzoic acid, this is an organic compound. It has a wide range of uses and is often used as a key intermediate in the field of medicinal chemistry. The unique properties of fluorine and iodine atoms can significantly affect the biological activity and physicochemical properties of compounds. By introducing it into a specific drug molecular structure by chemical synthesis, it can enhance the affinity and selectivity of drugs to targets and improve drug efficacy. For example, in the development of some anti-cancer drugs, such intermediates can be used to optimize molecular structures and achieve better therapeutic effects.
In the field of materials science, it also has important applications. Because its structure gives special optoelectronic properties, it can be used to prepare organic optoelectronic materials. For example, in the development of organic Light Emitting Diode (OLED) materials, 5-fluoro-3-iodobenzoic acid can participate in the construction of luminescent layer or charge transport layer material, improve the luminous efficiency and stability of the material, and then improve the performance of OLED devices.
In the field of pesticide chemistry, it also plays an important role. As a raw material for synthesizing new pesticides, with its unique chemical structure, compounds with high insecticidal, bactericidal or herbicidal activities can be derived, and the presence of fluorine and iodine atoms can enhance the environmental stability and biological activity persistence of pesticides, providing more effective protection for agricultural production.
What are the synthesis methods of 5-fluoro-3-iodo-benzoic Acid?
The synthesis method of 5-fluoro-3-iodobenzoic acid is a very important topic in the field of organic synthesis. One of the common methods is to use benzoic acid as the starting material. The benzoic acid is first halogenated, and the fluorine atom on the benzene ring can be introduced through a specific halogenation reagent, such as under suitable conditions, the benzoic acid is reacted with a fluorine substitution reagent. Then, a suitable iodine substitution reagent is selected. When the reaction conditions are precisely controlled, such as temperature, solvent and catalyst, the iodine atom is replaced at the designated position of the benzene ring, that is, position 3, to obtain 5-fluoro-3-iodobenzoic acid.
Furthermore, a derivative of benzene can also be used as the starting material. For example, with a certain type of benzene derivative with a specific substituent, fluorine atoms and iodine atoms are gradually introduced through a series of organic reactions to achieve the synthesis of the target product. In this process, the reaction route needs to be rationally designed according to the characteristics of the selected starting material. For example, if the starting material has a functional group that is easy to convert, this functional group can be skillfully used to achieve precise substitution of fluorine and iodine atoms in an orderly manner through a multi-step reaction, and finally 5-fluoro-3-iodobenzoic acid can be generated.
In addition, similar compound synthesis strategies reported in the literature can also be used for reference. According to the structure characteristics of 5-fluoro-3-iodobenzoic acid, the reaction conditions and routes were adjusted and optimized to find a more efficient, convenient and economical synthesis path, so as to effectively obtain this compound.
What are the precautions for 5-fluoro-3-iodo-benzoic Acid in storage and transportation?
5-Fluoro-3-iodobenzoic acid is also an organic compound. During storage and transportation, many matters need to be paid attention to.
Storage first. This substance should be placed in a cool and dry place, away from direct sunlight. Due to light or photochemical reactions caused by it, the purity and stability of the substance are damaged. And the storage place should be away from fire and heat sources to prevent fires. Because it may have certain chemical activity, it may be dangerous to encounter open flames, hot topics.
Furthermore, it needs to be stored separately from oxidants, reducing agents, alkalis, etc., and must not be mixed. Gaiyin 5-fluoro-3-iodobenzoic acid may react with these substances easily, causing danger. In the warehouse, there should be suitable materials for containing leaks for emergencies.
As for transportation, it is necessary to ensure that the packaging is complete and the loading is secure before transportation. The packaging materials must be able to prevent leakage, rain and vibration. During transportation, the speed of the vehicle should not be too fast, and it is not allowed to brake abruptly to avoid material leakage due to package damage. The transportation vehicle should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. The escort personnel must be familiar with the nature of the goods transported and emergency treatment measures. During transportation, if there is an accident such as leakage, emergency measures should be taken immediately to evacuate the crowd, prevent the expansion of pollution, and report to the relevant departments in time.
In this way, 5-fluoro-3-iodobenzoic acid is safe during storage and transportation, and there is no risk of accidents.
What is the market price of 5-fluoro-3-iodo-benzoic Acid?
5-Fluoro-3-iodobenzoic acid, a key organic synthesis intermediate in the field of fine chemicals, is widely used in many industries such as medicine, pesticides, and material science. Its market price often fluctuates due to factors such as quality, purity, supply and demand situation, and transaction scale. It is difficult to generalize.
In the past, when the market supply was abundant and demand was relatively stable, its price was relatively close to the people. If a batch of products has a purity of more than 98% and a considerable number of bulk transactions, the price per gram may be in the tens of yuan. However, if the market supply shortage, such as lack of raw materials, obstacles to production processes, etc., causes the output to drop sharply, and the demand remains strong, the price will rise significantly.
Furthermore, there are differences in the prices sold by different suppliers. Large enterprises with advanced production technology and strict quality control system have high product quality and slightly higher prices; while some small manufacturers, in order to gain market share, may sell at lower prices, but the product quality may be uneven.
If the required purity is extremely high, such as for high-end pharmaceutical research and development, products with 99% or higher purity must be much higher than those with ordinary purity. In addition, the international situation, exchange rate fluctuations, and transportation costs will also affect their prices. In case of international trade friction, increased tariffs, or rising costs in transit will all be transmitted to product prices, causing them to rise. Therefore, in order to know the exact market price, we should consult relevant suppliers in detail and consider various factors in order to obtain more accurate price information.