2 Fluoro 4 Iodonicotinic Acid
Iodobenzene

2-fluoro-4-iodonicotinic Acid

Fengxi Chemical

Specifications

HS Code

549986

Chemical Formula C6H3FINO2
Molar Mass 267.00 g/mol
Appearance Solid (usually white to off - white powder)
Melting Point Data - specific value may vary, needs experimental determination
Boiling Point Data - specific value may vary, needs experimental determination
Solubility In Water Limited solubility, due to its polar - non - polar nature balance
Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO, DMF
Density Data - specific value may vary, needs experimental determination
Pka Value Data - specific value may vary, needs experimental determination
Stability Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula C6H3FINO2
Molar Mass 253.00 g/mol
Appearance Solid (usually white to off - white)
Melting Point Data specific to pure sample needed (expected to be in a certain range for organic acids)
Solubility In Water Low solubility due to non - polar aromatic and halogenated groups
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Pka Value related to its acidic nature, specific experimental determination required for accurate value
Density Data specific to pure sample needed
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
Name 2-fluoro-4-iodonicotinic Acid
Chemical Formula C6H3FINO2
Molar Mass 271.00 g/mol
Appearance Solid (likely white or off - white)
Solubility In Water Low solubility, as it's an organic acid with non - polar groups
Pka Around 3 - 4 (estimated for the carboxylic acid group)
Boiling Point Decomposes before boiling (due to presence of iodine and fluorine)
Hazard Class Irritant (may cause irritation to skin, eyes, and respiratory tract)
Chemical Formula C6H3FINO2
Molar Mass 271.00 g/mol
Appearance Solid (likely a white or off - white powder)
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO
Melting Point Data may vary, but generally in the range of 150 - 200°C (approximate)
Boiling Point Decomposes before boiling in normal conditions
Pka Around 3 - 4 (approximate for the carboxylic acid group)
Stability Stable under normal conditions, but sensitive to light and moisture
Packing & Storage
Packing 100g of 2 - fluoro - 4 - iodonicotinic Acid packaged in a sealed, chemical - resistant bottle.
Storage 2 - fluoro - 4 - iodonicotinic acid should be stored in a cool, dry place away from heat and direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and contact with air, which could potentially lead to degradation. Store it separately from incompatible substances, such as strong oxidizing agents or bases, to avoid chemical reactions.
Shipping 2 - fluoro - 4 - iodonicotinic acid is shipped in well - sealed, corrosion - resistant containers. It adheres to strict chemical shipping regulations. Shipment ensures protection from physical damage and environmental factors during transit.
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2-fluoro-4-iodonicotinic Acid 2-fluoro-4-iodonicotinic Acid 2-fluoro-4-iodonicotinic Acid
General Information
Frequently Asked Questions
What are the main uses of 2-fluoro-4-iodonicotinic acid?
2-% hydroxyl-4-mercaptobenzoic acid is a very important organic compound with a wide range of uses and key applications in many fields.
In the field of medicinal chemistry, this compound is often used as an intermediate in drug synthesis. Due to its special chemical structure, it has certain biological activity and reactivity, and can participate in the construction process of many drug molecules. For example, it can be integrated into the structure of drug molecules through specific chemical reactions, thereby improving the solubility, stability and bioavailability of drugs, and making great contributions to the development of new and efficient drugs.
In the field of materials science, 2-% hydroxyl-4-mercaptobenzoic acid also shows a unique role. Its thiol groups can coordinate with a variety of metal ions to form stable complexes. This property makes it a modifier or stabilizer when preparing metal nanomaterials. By regulating its interaction with metal ions, the size, morphology and dispersion of nanomaterials can be effectively controlled, so that nanomaterials with specific properties can be prepared, such as functional materials used in catalysis, sensing and other fields.
In the field of chemical analysis, this compound can be used as an analytical reagent. Because it can react specifically with certain metal ions or compounds to generate products with specific color or optical properties, it can be used for qualitative or quantitative analysis of these substances. For example, the light absorption properties of complexes formed with specific metal ions can be used to determine the content of the metal ions in the sample by spectrophotometry.
In addition, in the field of organic synthetic chemistry, the carboxyl and hydroxyl groups of 2-% hydroxyl-4-mercaptobenzoic acid can participate in a variety of classical organic reactions, such as esterification reactions, condensation reactions, etc., providing a basic structural unit for the construction of more complex organic compound molecules, enabling organic synthesis chemists to design and synthesize a variety of novel organic compounds.
What are the synthesis methods of 2-fluoro-4-iodonicotinic acid?
To prepare 2-alkynyl-4-ketovaleric acid, the following methods can be used.
First, ethyl propionate and ethyl acetoacetate are used as starting materials. First, the alkynyl group of ethyl propionate interacts with a strong base, such as using sodium hydride and alkynyl to deproton to form a carboanion, which is quite active. Then, it is nucleophilic added to the carbonyl group of ethyl acetoacetate to form a key intermediate product. This intermediate product is hydrolyzed, and under acidic conditions, the ester group is hydrolyzed to a carboxyl group. At the same time, the acetyl group undergoes ketogenic decomposition. After appropriate adjustment of the reaction conditions, 2-alkynyl-4-ketovaleric acid can be obtained.
Second, acetylene and diethyl 3-oxoglutarate are used as raw materials. Acetylene first reacts with sodium metal to form sodium acetylene, which is a strong nucleophilic reagent. Diethyl 3-oxoglutarate has a carbonyl group, and sodium acetylene attacks its carbonyl group nucleophilically and introduces an alkynyl group. The diethyl ester group is converted into a carboxyl group through a subsequent hydrolysis step, and attention should be paid to controlling the reaction conditions to prevent overreaction, and then the target product can be obtained.
Third, 2-bromo-4-ketovaleric acid can be considered as a substrate to utilize alkynylation. Nucleophilic substitution reaction occurs with 2-bromo-4-ketovaleric acid with alkynyl lithium reagents, such as lithium acetylene. The alkynyl group of lithium alkynyl replaces the bromine atom to form 2-alkynyl-4-ketovaleric acid. In this process, the reaction solvent, temperature and other conditions need to be controlled in detail to improve the reaction yield and selectivity.
All methods have advantages and disadvantages. In actual operation, the choice is weighed according to many factors such as the availability of raw materials, the difficulty of controlling the reaction conditions, the purity and yield of the product, in order to find the best synthesis path.
What are the physical properties of 2-fluoro-4-iodonicotinic acid?
The physical properties of 2-% hydroxy- 4-chlorobenzoic acid are as follows:
This substance is mostly in the state of white crystalline powder at room temperature, and the texture is fine. When smelled, there is little special odor emitted, which makes it not disturbing due to odor when used in many scenarios.
When it comes to solubility, 2-hydroxy- 4-chlorobenzoic acid is slightly soluble in water. Water is the source of life, and everything is related to it. However, this substance has limited solubility in water, can only dissolve a little, and is difficult to disperse in a large proportion in aqueous solution. However, it shows good solubility in organic solvents such as ethanol and ether. Ethanol and ether are the common choice of organic solvents. 2-hydroxy- 4-chlorobenzoic acid can be better dispersed in it, just like fish get water. This characteristic can be used in chemical preparation, drug extraction and other fields. It can be used to extract and separate this substance with organic solvents.
Its melting point is quite considerable, about 150-152 ° C. For the melting point, the critical temperature at which the substance changes from solid to liquid. The melting point value of 2-hydroxy- 4-chlorobenzoic acid indicates that its solid structure is relatively stable. To melt it, it needs to reach such a temperature. This characteristic is of great significance in material processing and other aspects. If this substance needs to be processed in liquid form, it must reach this temperature range.
Furthermore, the density of 2-hydroxy- 4-chlorobenzoic acid is about 1.49 g/cm ³. The density is the mass per unit volume of the substance. This value shows that it has certain weight characteristics compared with common substances. When storing and transporting, it is necessary to arrange the container and load reasonably according to its density to ensure the stability of the process.
In summary, the physical properties of 2-hydroxy- 4-chlorobenzoic acid have a great impact on the application of chemical industry, medicine and many other fields. Only when its properties are known can it be used.
What is the market price of 2-fluoro-4-iodonicotinic acid?
At present, the price of 2-hydroxy- 4-chlorobenzoic acid sold in the market varies due to various reasons. First, the purity of this drug is essential. If its purity is extremely high and there are few impurities, the price will be high; on the contrary, if it contains a lot of heterogeneity, the purity is extremely low, and the price will also drop. If the cover is high in purity, the preparation method must be complex, and it requires a lot of material resources and manpower, so the price is expensive.
Second, the scale of production also affects its price. If the workshop makes this product on a large scale and the benefits of the scale, the unit production cost will decrease, and the price may be slightly lower; if it is a small work, the quantity is small and the cost is high, and it is sold in the market, the price is not cheap.
Third, the supply and demand of the city is also the key. If the current pharmaceutical, chemical and other industries are eager for this material, but the supply is limited, the price will increase; if the supply exceeds the demand, the goods are accumulated in the warehouse, and the merchants want to sell it quickly, the price will be reduced.
Fourth, the price of raw materials also has an impact. For raw materials made of 2-hydroxy- 4-chlorobenzoic acid, if the price goes up, the price of the finished product will also go up; if the price of raw materials goes down, the price of the finished product may go down.
And transportation fees and taxation regulations are all related to the market price. Shipping from a long way, plus travel costs and insured prices, the price will increase; those with heavy taxes will also raise the price in order to protect their profits. In short, the market price of 2-hydroxy- 4-chlorobenzoic acid is the result of the interaction of various factors. If you want to know its actual price, you must study it in detail in the market.
In which fields is 2-fluoro-4-iodonicotinic acid used?
In the field of medicine, it can be used as a raw material for drug synthesis. Due to its unique structure, it can participate in the construction of many drug molecules, helping to develop good drugs for treating specific diseases. For example, some drugs targeting nervous system diseases, 2% tibia-4-guanidine butyric acid may play a key role in it, or help to regulate the transmission of neurotransmitters, which is beneficial for alleviating the symptoms of nervous system disorders.
In the field of biochemical research, it is an important bioactive substance. Scientists can improve their understanding of life processes by studying its metabolic pathways and mechanisms of action in organisms. For example, in the investigation of cell signaling pathways, 2-% tibia-4-guanidine butyric acid may participate in it, affecting the information exchange between cells, thereby regulating important physiological activities such as cell growth and differentiation.
In the field of agriculture, it also has its place. It can be used as a component of plant growth regulators to affect the growth and development of plants. It can regulate the balance of plant hormones, promote the growth of plant roots, and enhance the tolerance of plants to environmental stress, such as improving plant stress resistance, so that it can still grow well in adverse environments such as drought and salinity, thereby improving the yield and quality of crops.
In the field of food additives, because it has certain biological activities, it can be used as a functional food additive. Added to specific foods, it can supplement the human body with special nutrients, exert health benefits, and provide a different choice for people who pursue a healthy diet.