2 Hydroxy 3 5 Diiodobenzoate
Iodobenzene

2-hydroxy-3,5-diiodobenzoate

Fengxi Chemical

Specifications

HS Code

795132

Chemical Formula C7H3I2O3
Molar Mass 397.906 g/mol
Appearance Typically a solid (description may vary by form)
Solubility In Water Limited solubility (exact value would need experimental determination)
Melting Point Data would require experimental measurement
Boiling Point Likely decomposes before boiling (specific data needs experiment)
Density Experimental determination required for accurate value
Acidity Pka Value depends on the dissociation behavior, experimental measurement needed
Color May be colorless to off - white (subject to form and purity)
Odor May be odorless or have a faint characteristic odor (if any)
Name 2-hydroxy-3,5-diiodobenzoate
Chemical Formula C7H3I2O3 -
Molecular Weight 393.909 g/mol
Appearance Solid (predicted)
Solubility In Water Low (predicted)
Pka Around 2 - 3 (estimated for phenolic - OH)
Boiling Point Decomposes before boiling (predicted)
Color Colorless to light - colored solid (predicted)
Chemical Formula C7H3I2O3
Molar Mass 395.909 g/mol
Appearance Solid (likely white or off - white powder)
Solubility In Water Low solubility, due to non - polar benzene ring and relatively large iodine atoms
Solubility In Organic Solvents Soluble in some polar organic solvents like DMSO, DMF, due to the polar carboxylate and hydroxyl groups
Melting Point Requires experimental determination, likely in the range of organic aromatic carboxylates (above 100°C, speculation based on similar structures)
Boiling Point Decomposes before boiling, due to the presence of iodine and the sensitivity of the benzoate structure
Pka Of The Hydroxyl Group Approximately 9 - 10 (estimation, similar to phenol derivatives with electron - withdrawing groups)
Pka Of The Carboxyl Group Around 3 - 4 (typical for benzoic acid derivatives)
Odor Odorless or faint, characteristic of aromatic carboxylates
Name 2-hydroxy-3,5-diiodobenzoate
Chemical Formula C7H3I2O3
Molar Mass 397.908 g/mol
Appearance Solid (presumably, common for benzoate salts)
Solubility In Water Varies based on counter - ion (if in salt form), generally limited solubility of the free acid
Solubility In Organic Solvents May dissolve in polar organic solvents like ethanol to some extent
Pka For The Carboxylic Acid Group Typical benzoic acid pKa around 4 - 5, but the iodo and hydroxy groups may affect it
Packing & Storage
Packing 100 - gram vial of 2 - hydroxy - 3,5 - diiodobenzoate, tightly sealed for chemical safety.
Storage 2 - hydroxy - 3,5 - diiodobenzoate should be stored in a cool, dry place, away from direct sunlight. Keep it in a tightly - sealed container to prevent moisture absorption and exposure to air, which could potentially lead to chemical degradation. Store it separately from incompatible substances like strong oxidizing agents and bases to avoid dangerous reactions.
Shipping 2 - hydroxy - 3,5 - diiodobenzoate is shipped in accordance with strict chemical transportation regulations. Packed in corrosion - resistant containers, it's transported by specialized carriers to ensure safe and compliant delivery.
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2-hydroxy-3,5-diiodobenzoate 2-hydroxy-3,5-diiodobenzoate 2-hydroxy-3,5-diiodobenzoate
General Information
Frequently Asked Questions
What are the chemical properties of 2-hydroxy-3,5-diiodobenzoate?
2-Hydroxy-3,5-diiodobenzoate is one of the organic compounds. Its chemical properties are unique and worth studying.
This compound has acidic properties. Due to its carboxyl group (-COOH), under suitable conditions, protons can be released and the reaction is acidic. It can neutralize with alkali substances to produce corresponding salts and water. For example, when reacted with sodium hydroxide, the hydrogen in the carboxyl group combines with hydroxide to form water, and the rest forms salts, which is an important acid-base reaction property.
Furthermore, the hydroxyl group (-OH) in its molecule is also active. Hydroxyl groups can participate in many reactions, such as esterification reactions. Under the condition of acid catalysis, it can react with alcohols to form ester bonds and derive new ester compounds. This reaction is widely used in the field of organic synthesis.
The iodine atom in the molecule has a great influence on the properties of the compound due to the electronegativity and atomic radius of iodine. The iodine atom increases the polarity of the molecule, which in turn affects its solubility. In organic solvents, its solubility may be better than that of some similar compounds without iodine. And iodine atoms can participate in reactions such as nucleophilic substitution, introducing new functional groups to the compound and expanding its chemical transformation path.
2-Hydroxy-3,5-diiodobenzoate is rich in chemical properties and may have potential application value in organic synthesis, medicinal chemistry and other fields. Novel compounds and practical products can be developed through in-depth exploration and rational utilization of its chemical properties.
What are the common uses of 2-hydroxy-3,5-diiodobenzoate?
2-Hydroxy-3,5-diiodobenzoate is an organic compound that is commonly used in chemical, pharmaceutical and other fields. Its common uses are as follows:
First, in the field of medicine, it has antibacterial and anti-inflammatory effects. Because it contains iodine, it has inhibitory and killing effects on a variety of bacteria and fungi, and can be used to prepare antibacterial drugs to deal with skin infections, respiratory tract infections and other diseases. Such as some topical ointments or sprays, it contains this ingredient to help reduce inflammation and promote wound healing.
Second, in the chemical industry, it can be used as an organic synthesis intermediate. With its special chemical structure, it can participate in many organic reactions and synthesize more complex organic compounds. For example, in the synthesis of certain polymer materials with specific functions, it can be used as a starting material to build the desired molecular structure through a series of reactions, thus endowing the material with unique properties, such as good solubility, thermal stability, etc.
Third, analytical chemistry can be used for the detection and quantitative analysis of specific metal ions. Because it can form complexes with certain metal ions with specific properties, the accurate determination of metal ions can be achieved by detecting the related properties of the complexes, such as color change, absorbance, etc. For example, in water quality testing, it can be used to detect the content of certain heavy metal ions, providing an important basis for water quality assessment. In conclusion, 2-hydroxy-3,5-diiodobenzoate is widely used and plays a key role in many fields, which is of great significance to promoting the development of related industries.
What is the synthesis method of 2-hydroxy-3,5-diiodobenzoate?
2-Hydroxy-3,5-diiodobenzoate is 2-hydroxy-3,5-diiodobenzoate, the method of synthesizing this compound is as follows:
The starting material is often 2-hydroxy benzoic acid (salicylic acid). First iodize the salicylic acid. Take an appropriate amount of salicylic acid, place it in a suitable reaction vessel, and add an appropriate amount of solvent, such as glacial acetic acid, to help dissolve. After stirring well, slowly add an iodizing agent, such as a mixed system of iodine elemental ($I_2 $) and hydrogen peroxide ($H_2O_2 $). $H_2O_2 $is used here as an oxidizing agent to promote the electrophilic substitution reaction between iodine elemental and salicylic acid. During the reaction process, it is necessary to control the reaction temperature, generally maintained at a low temperature, such as 0-5 ° C. This is because the reaction is more intense, low temperature helps the reaction proceed smoothly, and can improve the selectivity of the reaction, so that the iodine atoms are mainly replaced at the 3 and 5 positions. At the same time, closely observe the reaction phenomena, such as the color change of the solution.
After the iodization reaction is completed, 2-hydroxy-3,5-diiodobenzoic acid is obtained. Then the esterification reaction is carried out, and the 2-hydroxy-3,5-diiodobenzoic acid is mixed with the corresponding alcohol (the appropriate alcohol is selected according to the structure of the desired benzoate ester), and an appropriate amount of concentrated sulfuric acid is added as a catalyst. Concentrated sulfuric acid can promote the esterification reaction and speed up the reaction rate. In order to move the reaction forward, a water separator or other device can be used to remove the water generated by the reaction. The reaction temperature needs to be adjusted according to the boiling point of the selected alcohol, and the reaction is generally refluxed under heating conditions for several hours. After the reaction is completed, the reaction mixture is post-treated. First, an appropriate amount of sodium bicarbonate solution is used to neutralize the sulfuric acid in the reaction system, so that the solution is weakly basic. This step can avoid the effect of acidic conditions on the product. Then the liquid separation operation is carried out to collect the organic phase. The organic phase is dried with a desiccant such as anhydrous sodium sulfate to remove the remaining moisture. Finally, the product is purified by reduced pressure distillation or column chromatography to obtain a pure 2-hydroxy-3,5-diiodobenzoate. In this way, the synthesis of 2-hydroxy-3,5-diiodobenzoate is completed.
In which fields is 2-hydroxy-3,5-diiodobenzoate used?
2-Hydroxy-3,5-diiodobenzoate is used in many fields such as medicine and chemical industry.
In the field of medicine, it is often a key intermediate in drug synthesis. The introduction of iodine atoms can significantly change the physical and chemical properties of compounds, and have a great impact on the activity, stability and targeting of drug molecules. Many antibacterial, antiviral and anti-tumor drugs are often developed and synthesized by this substance. It may be able to use specific chemical reactions to cleverly connect with other organic molecules to construct compounds with complex structures and unique pharmacological activities, opening up a broad path for the treatment of diseases and the creation of new drugs.
In the chemical industry, this compound also has important uses in the synthesis of fine chemicals. In the preparation of coatings, pigments and dyes, it can be added as a functional additive. With its special chemical structure, it can improve the color fastness, weather resistance and adhesion of products. For example, in the manufacture of high-end coatings, the appropriate addition of 2-hydroxy-3,5-diiodobenzoate can improve the stability and durability of coatings in complex environments, so that the coated surface can remain in good condition for a long time.
In addition, in the field of materials science, with the in-depth development of research, its potential applications have also attracted increasing attention. It is expected to act as a structural regulator in the synthesis of new polymer materials, regulating the crystallization, thermal stability and mechanical properties of polymer materials, and providing new ideas and raw material selection for the research and development of high-performance materials.
In short, 2-hydroxy-3,5-diiodobenzoate plays an indispensable role in many fields due to its unique chemical structure, and with the progress of science and technology, its application prospects will be broader.
What is the market outlook for 2-hydroxy-3,5-diiodobenzoate?
For 2-hydroxy-3,5-diiodobenzoate, the market situation and prospects are really related to many considerations. In today's world, in the field of pharmaceutical chemistry, this compound may have potential uses in drug research and development due to its unique chemical properties.
Observing the situation of the pharmaceutical industry, the development of new drugs is an ever-present priority. 2-hydroxy-3,5-diiodobenzoate may provide a key intermediary for drug synthesis, and its structural properties may guide chemists to create novel drug molecules to meet the needs of many diseases. Such as the exploration of therapeutic drugs for specific inflammation and tumors, or the intervention of this compound, new paths have been obtained.
In the field of chemical production, the sophistication of its synthesis process is related to the supply and cost of this product in the market. If an efficient and environmentally friendly synthesis method can be developed to improve the efficiency of production and reduce the cost, it will be able to expand its use and increase its market share.
However, the market prospect is not completely smooth. Regulations and policies restrict whether this product can enter the market in compliance. The supervision of pharmaceutical chemical products in various countries is increasingly strict, from Quality Standards to Environmental Impact, there are meticulous regulations. If 2-hydroxy-3,5-diiodobenzoate wants to be commercialized on a large scale, it must follow these rules to be safe.
Furthermore, the situation of competitors should not be ignored. The progress of research and development of similar compounds or substitutes can challenge their market position at any time. If there are better alternatives available, cheap and effective, the market prospect of 2-hydroxy-3,5-diiodobenzoate may be bleak.
In summary, although 2-hydroxy-3,5-diiodobenzoate has potential opportunities in the field of pharmaceutical and chemical industry, it also faces many challenges such as regulations and competition. The clarity of its market prospects depends on the efforts and opportunities of R & D, production and market operation.