3 Iodo 4 Methylbenzoate
Iodobenzene

3 Iodo 4 Methylbenzoate

Fengxi Chemical

Specifications

HS Code

271156

Name 3-iodo-4-methylbenzoate
Molecular Formula C9H9IO2
Molar Mass 276.07 g/mol
Appearance Solid (likely)
Solubility In Water Low (expected, as it's an organic ester with an iodo group)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone (expected due to its organic nature)
Stability Stable under normal conditions (but iodine - containing compounds may be sensitive to light and heat in some cases)
Chemical Formula C9H9IO2
Molecular Weight 262.07
Appearance Solid (predicted)
Solubility In Water Insoluble (predicted)
Solubility In Organic Solvents Soluble in common organic solvents (predicted)
Chemical Formula C9H9IO2
Molar Mass 276.07 g/mol
Appearance Solid (predicted from similar compounds)
Solubility In Water Low (due to non - polar aromatic part)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Chemical Formula C9H9IO2
Molecular Weight 262.07
Appearance Solid (Typical appearance of the compound)
Melting Point Specific melting point data if available
Boiling Point Specific boiling point data if available
Solubility In Water Limited solubility (General indication)
Solubility In Organic Solvents Soluble in common organic solvents (General indication)
Density Specific density value if available
Flash Point Specific flash point data if available
Vapor Pressure Specific vapor pressure data if available
Odor Characteristic odor (If known)
Stability Stable under normal conditions (General indication)
Packing & Storage
Packing 100g of 3 - iodo - 4 - methylbenzoate packaged in a sealed, labeled chemical - grade bottle.
Storage 3 - iodo - 4 - methylbenzoate should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and strong oxidizing agents. Store in a tightly sealed container to prevent exposure to air and moisture, which could potentially lead to degradation. It should be isolated from incompatible substances to avoid chemical reactions.
Shipping 3 - iodo - 4 - methylbenzoate is shipped in well - sealed containers, compliant with chemical transport regulations. Packaging ensures protection from damage and leakage during transit, with proper labeling for hazard identification.
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3-iodo-4-methylbenzoate 3-iodo-4-methylbenzoate 3-iodo-4-methylbenzoate
General Information
Frequently Asked Questions
What is the chemical structure of 3-iodo-4-methylbenzoate?
3-Iodo-4-methylbenzoate is one of the organic compounds. Its chemical structure can be analyzed as follows:
"benzoate" means benzoate. The structure of benzoic acid is that a benzene ring is connected to a carboxyl group (-COOH). When the hydrogen atom of the carboxyl group is replaced by other groups, it becomes a benzoate ester compound.
"3-iodo" indicates that in the benzoate structure, the No. 3 position of the benzene ring is replaced by an iodine atom (I). The so-called number of the benzene ring is the number 1 position of the carbon atom connected to the carboxyl group, which is numbered in sequence according to the benzene ring.
"4-methyl" means that the benzene ring is connected with methyl at position 4. In the case of methyl, a group composed of one carbon atom and three hydrogen atoms.
In summary, the chemical structure of 3-iodo-4-methylbenzoate is that the benzene ring of the benzoate ester has iodine atom at position 3 and methyl at position 4. This structure endows the compound with specific physical and chemical properties, which may be of important significance in organic synthesis, medicinal chemistry and other fields. Its structural characteristics affect its reactivity, solubility and other properties, and are also the basis for related research and applications.
What are the main uses of 3-iodo-4-methylbenzoate?
3-Iodo-4-methylbenzoate is 3-iodo-4-methylbenzoate, which has a wide range of uses. In the field of pharmaceutical chemistry, it is often a key intermediate. The creation of many drugs requires this as the starting material, through a series of delicate chemical reactions, to construct complex structures with specific pharmacological activities. Because of the unique electronic effect and steric resistance of iodine atoms and methyl groups in the structure, it can endow drugs with unique properties, help drugs better fit the target and improve the efficacy.
In the field of materials science, it also plays an important role. It can participate in the preparation of functional polymer materials, such as as polymeric monomers, and react with other monomers to form polymers with special optical and electrical properties. The synthesized polymers may emerge in the fields of optoelectronic materials, sensors, etc., expanding new paths for the functionalization of materials.
Furthermore, in organic synthetic chemistry, it is an extremely useful synthetic block. Chemists rely on its structural characteristics to take advantage of the activity of iodine atoms to carry out coupling reactions, etc., so as to realize the construction of carbon-carbon bonds and carbon-heteroatomic bonds, and achieve efficient synthesis of various complex organic compounds, greatly enriching the types and structures of organic compounds.
What are the physical properties of 3-iodo-4-methylbenzoate?
3-Iodo-4-methylbenzoate is one of the organic compounds. Its physical properties are quite impressive. First, when it comes to appearance, it is often white to light yellow crystalline powder or solid. This form is more common in many organic compounds, just like many similar substances. It is shown in this form for easy observation and processing.
Furthermore, the melting point is one of its important physical properties. However, the specific melting point value varies due to different experimental conditions and differences in purity, and is roughly within a specific temperature range. The determination of the melting point is like a key to explore the properties of a substance, which can help chemists determine its purity and conduct subsequent analysis.
Its solubility cannot be ignored. In organic solvents such as ethanol and acetone, there is a certain solubility, just like a fish entering water, it can blend with these organic solvents to form a uniform system. However, in water, the solubility is poor, just like the incompatibility of oil and water. This property is closely related to its molecular structure. The polarity of the molecule and other factors determine its solubility in different solvents.
In addition, the boiling point is also an aspect of its physical properties. Although the exact boiling point data is also affected by many factors, its boiling point reflects the energy conditions required for the material to change from liquid to gas, providing an important reference for the separation and purification of substances in chemical production and experimental operations.
In terms of density, although there is no precise and uniform value, it affects its distribution and related physical behavior in the mixture to a certain extent, just as the weight of the object affects its position in space.
In summary, the physical properties of 3-iodo-4-methylbenzoate, such as appearance, melting point, solubility, boiling point, density, etc., are the key elements for understanding and studying this compound. Chemists can use this to gain a deeper understanding of its properties, and then make good use of it in many fields such as organic synthesis and drug development.
What are 3-iodo-4-methylbenzoate synthesis methods?
The synthesis methods of 3-iodine-4-methylbenzoate are quite diverse. The methods of the past rely on classical organic synthesis techniques.
First, 4-methylbenzoic acid can be started. Shilling 4-methylbenzoic acid reacts with appropriate halogenating reagents, such as iodine and specific catalysts, under suitable reaction conditions to introduce iodine atoms to obtain 3-iodine-4-methylbenzoic acid. Subsequently, this product and alcohols, with the help of acid catalysis or coupling reagents, undergo esterification reaction to obtain 3-iodine-4-methylbenzoate.
There are also 4-methylbenzaldehyde as raw materials. It is first oxidized to 4-methylbenzoic acid, and then carried out according to the above steps of introducing iodine atoms and esterification. The oxidation method can be used with common oxidants, such as potassium permanganate.
In addition, from aromatic hydrocarbons containing iodine and methyl, the equivalent of carboxyl group can be introduced through Fu-gram acylation reaction, and then converted into ester group. When reacting, it is necessary to pay attention to the activity of reagents, reaction temperature, time, and solvent selection, which are all related to the success or failure of the reaction and the yield. Different synthesis paths have their own advantages and disadvantages, and need to be selected according to factors such as the availability of actual required raw materials, cost, and purity of the target product.
3-iodo-4-methylbenzoate are there any precautions during storage and transportation?
3-Iodo-4-methylbenzoate is an organic compound. When storing and transporting it, many key matters need to be paid attention to.
When storing, the first choice of environment. It should be placed in a cool and dry place, away from heat sources and open flames. This is because organic compounds are flammable. When heated or exposed to open flames, it is very easy to cause fire or even risk explosion. And humid environments may also cause chemical reactions such as hydrolysis, which can damage quality.
Furthermore, attention should be paid to isolation from other substances. Avoid co-storage with oxidants, strong acids, strong bases, etc. Due to the chemical structure of 3-iodo-4-methylbenzoate, it comes into contact with oxidants or undergoes a violent oxidation reaction; it encounters with strong acids and alkalis, or causes hydrolysis of ester groups, causing it to deteriorate.
Packaging should not be ignored. A well-sealed packaging material should be used to prevent leakage. If it is solid, it can be lined with plastic bags, paper bags, etc., plus iron drums or plastic drums; if it is liquid, a special chemical-resistant container should be used to ensure a tight seal.
When transporting, the first thing to ensure is that the means of transportation are clean and dry. Do not leave residues that may react with it. And during transportation, be sure to prevent violent vibration and collision. Because it is a fragile item, vibration and collision or packaging damage can cause leakage.
At the same time, transportation personnel should also have professional knowledge and know the characteristics of the compound and emergency treatment methods. In the event of leakage and other accidents, timely and correct responses can be made to reduce hazards. In short, when storing and transporting 3-iodo-4-methylbenzoate, care should be taken in terms of environment, packaging, isolation and personnel knowledge to ensure safety.