2 Methyl 5 Iodobenzoic Acid
Iodobenzene

2 Methyl 5 Iodobenzoic Acid

Fengxi Chemical

Specifications

HS Code

765375

Chemical Formula C8H7IO2
Molar Mass 264.04 g/mol
Appearance Solid
Physical State At Room Temperature Solid
Solubility In Water Low solubility
Melting Point 145 - 149 °C
Boiling Point Decomposes before boiling
Odor Odorless (usually)
Acidity Pka Typical benzoic acid - like pKa around 4 - 5 (approximate)
Packing & Storage
Packing 100g of 2 - methyl - 5 - iodobenzoic acid packaged in a sealed, labeled plastic bottle.
Storage 2 - Methyl - 5 - iodobenzoic acid should be stored in a cool, dry place away from direct sunlight. Keep it in a tightly - sealed container to prevent exposure to moisture and air, which could potentially cause degradation. Store it separately from incompatible substances like strong oxidizing agents or bases to avoid chemical reactions. Ensure the storage area is well - ventilated.
Shipping 2 - methyl - 5 - iodobenzoic acid is shipped in well - sealed, corrosion - resistant containers. It's transported under conditions avoiding heat, ignition sources, and contact with incompatible substances to ensure safe transit.
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2-methyl-5-iodobenzoic Acid 2-methyl-5-iodobenzoic Acid 2-methyl-5-iodobenzoic Acid
General Information
Frequently Asked Questions
What are the physical properties of 2-methyl-5-iodobenzoic Acid?
2-Methyl-5-iodobenzoic acid is a kind of organic compound. It has specific physical properties, which are described as follows:
Looking at its appearance, it is usually a white to off-white crystalline powder. This appearance characteristic is easy to identify and is the primary observation point in many chemical experiments and industrial production processes.
When talking about the melting point, it is about 168-172 ° C. The melting point is one of the important physical constants of a substance, which is of great significance for determining the purity of the compound and identifying the substance. By accurately measuring the melting point, it can be determined whether it meets the corresponding Quality Standards.
In terms of solubility, it is slightly soluble in water. Water is a common solvent, and this property indicates that the interaction between the compound and water molecules is weak. However, it is soluble in organic solvents such as ethanol and ether. This difference in solubility provides a key basis for the separation, purification and choice of reaction medium of the compound. In organic synthesis, a suitable solvent can be selected according to its solubility to promote the smooth progress of the reaction.
In addition, the physical properties such as the density and stability of the compound are also worthy of attention. Density is related to the relationship between the mass and volume of a substance. Although the exact value may vary depending on the measurement conditions, it is very important in specific fields, such as the measurement of materials in chemical production. In terms of stability, the compound has certain stability under normal storage and use conditions. However, under special conditions such as high temperature and strong oxidants, or chemical reactions occur, the stability will be affected.
The physical properties of 2-methyl-5-iodobenzoic acid are of critical significance in the fields of chemical research, drug synthesis and materials science. With an understanding of its physical properties, researchers can carry out related work more effectively.
What are the chemical properties of 2-methyl-5-iodobenzoic Acid?
2-Methyl-5-iodobenzoic acid, an organic compound composed of a benzene ring, a carboxyl group, a methyl group, and an iodine atom. Its chemical properties are unique, with the following numbers:
First, the acidity is significant. The presence of carboxyl groups allows it to dissociate hydrogen ions in water and exhibit acidity. It can neutralize with bases to form corresponding salts and water. For example, when reacted with sodium hydroxide, 2-methyl-5-iodobenzoate and water are formed. This property is often used in organic synthesis for acid-base neutralization to adjust the pH of the reaction system, and can also be used to separate and purify compounds.
Second, the properties of halogenated aromatics are prominent. The iodine atoms on the benzene ring are highly active and can participate in a variety of nucleophilic substitution reactions. For example, under appropriate reaction conditions, iodine atoms can be replaced by nucleophilic reagents such as hydroxyl and amino groups, and then a series of derivatives can be synthesized. This reaction provides an important way to construct diverse organic compound structures.
Third, the influence of methyl group cannot be ignored. Methyl group is the power supply radical, which can affect the electron cloud density of the benzene ring through induction effect and superconjugation effect, thereby changing the reactivity of each position on the benzene ring. Due to the joint action of methyl group and iodine atom localization effect, the specific position on the benzene ring is more prone to electrophilic substitution reaction, which is of great significance for the design of organic synthesis routes.
Fourth, it is easy to decompose when heated At a certain temperature, 2-methyl-5-iodobenzoic acid may decompose to form products such as carbon dioxide and iodine-containing small molecules. Therefore, during storage and use, attention should be paid to temperature control to ensure its stability.
Fifth, it can participate in the esterification reaction. Under the action of catalysts such as concentrated sulfuric acid, carboxyl groups can be esterified with alcohols to form 2-methyl-5-iodobenzoic acid esters. This reaction is widely used in the fields of fragrance, drug synthesis, etc., and can endow the products with unique aroma and pharmacological activity.
What are the main uses of 2-methyl-5-iodobenzoic Acid?
2-Methyl-5-iodobenzoic acid (2-methyl-5-iodobenzoic acid) is widely used in the field of organic synthesis.
First, it can be used as a key intermediate in pharmaceutical synthesis. When creating new drugs, this compound can be connected to the molecular structure of the drug through a specific chemical reaction, giving the drug a specific pharmacological activity. For example, some drugs with antibacterial and anti-inflammatory effects often use 2-methyl-5-iodobenzoic acid as the starting material in the synthesis path, and through multi-step reactions, the active ingredient of the drug is precisely constructed.
Second, it also has important uses in materials science. It can be chemically modified to introduce it into polymer materials, thereby changing the properties of the materials. For example, by copolymerizing it with specific polymer monomers, the resulting polymer materials can have unique optical, electrical or thermal properties, which are suitable for the preparation of materials with special functions, such as photoelectric conversion materials, sensor sensitive materials, etc.
Furthermore, in the field of dye synthesis, 2-methyl-5-iodobenzoic acid can be used as a raw material for the synthesis of new dyes. Through ingenious design of reaction steps, using its structural characteristics, dyes with unique colors and properties can be synthesized to meet the special needs of different industries for dyes, such as textile printing and dyeing, ink manufacturing, etc.
In addition, in organic chemistry research, it is also a commonly used model compound. By conducting in-depth research on the various chemical reactions they participate in, researchers can gain insight into the mechanism of organic reactions, explore the optimization of reaction conditions, and provide important reference for the theoretical and practical development of organic synthetic chemistry.
What are the synthetic methods of 2-methyl-5-iodobenzoic Acid?
The methods for preparing 2-methyl-5-iodobenzoic acid are various and each has its own length. One method can take 2-methylbenzoic acid as the initial material. Dissolve 2-methylbenzoic acid in an appropriate solvent, such as glacial acetic acid, which can provide a stable environment for the reaction. Then, add an appropriate amount of iodine, which is the key reagent for introducing iodine atoms into the reaction. At the same time, adding an appropriate catalyst, such as concentrated sulfuric acid, etc., concentrated sulfuric acid can speed up the reaction rate and make the reaction easier to proceed. At a certain temperature, it is often heated to reflux, so that it can fully react. In this process, iodine atoms replace hydrogen atoms at specific positions on the benzene ring to gradually generate 2-methyl-5-iodobenzoic acid. After the reaction is completed, through various steps such as cooling, crystallization, and filtration, the crude product can be obtained, and then purified by recrystallization to improve the purity of the product.
There is another method, which can first activate 2-methylbenzoic acid to make the benzene ring more reactive. If it is treated with a specific reagent, the electron cloud density on the benzene ring is changed. Then, an iodine source is introduced, such as a mixed system of potassium iodide and hydrogen peroxide. In this system, hydrogen peroxide can oxidize potassium iodide to form active iodine, and then substitution reaction occurs with the activated benzene ring. The reaction conditions also need to be carefully controlled, and the temperature and the proportion of reactants have a significant impact on the reaction results. After the reaction is completed, the same separation and purification steps are carried out to obtain pure 2-methyl-5-iodobenzoic acid.
During the preparation process, all methods need to pay attention to the proportion of reactants and the control of reaction conditions, so as to obtain high yield and purity products. When operating, it is also necessary to follow safety regulations and properly handle reagents and products to ensure the smooth and safe experiment.
2-methyl-5-iodobenzoic Acid in storage and transportation
For 2-methyl-5-iodobenzoic acid, pay attention to many matters during storage and transportation. This is an organic compound with specific chemical properties, so it needs to be properly disposed of.
First words storage. Because it may be sensitive to environmental factors, it should be placed in a cool, dry and well-ventilated place. Avoid direct sunlight, cover light or cause photochemical reactions to occur, which will damage its quality. Temperature is also critical. Excessive temperature or cause it to decompose and deteriorate should usually be controlled in an appropriate low temperature range. And it needs to be kept away from fire and heat sources. Because of its organic characteristics, or flammability, it is easy to cause danger when exposed to open flames and hot topics.
Furthermore, the storage place should be stored separately from oxidants and reducing agents. The chemical activity of this compound makes it possible to react violently when it comes into contact with other chemicals, causing safety accidents. At the same time, the storage container must be well sealed to prevent it from being damp and oxidized, and to prevent the loss of volatile components or pollution of the environment.
As for transportation, it should not be taken lightly. When handling, it must be handled lightly to prevent damage to the packaging container. Because it may be corrosive, if the packaging is damaged and leaked, it may injure personnel and pollute the environment. Transportation vehicles must also meet safety standards and be equipped with corresponding fire and emergency treatment equipment to prepare for emergencies. During transportation, pay close attention to environmental conditions such as temperature and humidity to ensure the safety of goods. All those involved in transportation should be familiar with the characteristics of the chemical and emergency treatment methods to deal with various situations.