3 Iodo 2 Methylbenzoic Acid
Iodobenzene

3 Iodo 2 Methylbenzoic Acid

Fengxi Chemical

Specifications

HS Code

285103

Chemical Formula C8H7IO2
Molar Mass 264.044 g/mol
Appearance Solid (usually off - white to light - colored powder)
Melting Point Specific value would require literature search
Boiling Point Specific value would require literature search
Solubility In Water Low solubility, as it is an organic acid with non - polar aromatic part
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Acidity It is a carboxylic acid, so it has acidic properties with a pKa value (specific value needs literature search)
Density Specific value would require literature search
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
Chemical Formula C8H7IO2
Molar Mass 264.044 g/mol
Appearance Solid
Physical State At Room Temp Solid
Melting Point 160 - 162 °C
Solubility In Water Slightly soluble
Pka Value Around 3 - 4 (estimated for benzoic acid derivatives)
Boiling Point Decomposes before boiling (organic acids with iodine substituent)
Odor Odorless or very faint odor
Stability Stable under normal conditions but may decompose on heating or in contact with strong oxidizing agents
Chemical Formula C8H7IO2
Molar Mass 264.044 g/mol
Appearance Solid (usually white or off - white powder)
Melting Point Typically in a certain range (experimental determination required)
Boiling Point Decomposes before boiling (organic acid with iodine - containing structure)
Solubility In Water Low solubility (organic acid with hydrophobic benzene ring and iodine atom)
Solubility In Organic Solvents Soluble in some polar organic solvents like ethanol, acetone
Acidity Weak acid, dissociates to release H+ in solution
Iodine Content Contains one iodine atom per molecule
Reactivity Can participate in reactions typical of benzoic acids and iodo - aromatic compounds, such as esterification, nucleophilic substitution
Name 3-iodo-2-methylbenzoic acid
Molecular Formula C8H7IO2
Molecular Weight 262.044 g/mol
Appearance Solid
Color Off - white to light yellow
Melting Point 146 - 148 °C
Solubility In Water Slightly soluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, methanol, chloroform
Stability Stable under normal conditions, but may be sensitive to light and heat
Packing & Storage
Packing 100g of 3 - iodo - 2 - methylbenzoic acid packaged in a sealed, labeled container.
Storage 3 - iodo - 2 - methylbenzoic acid should be stored in a cool, dry place away from 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, like strong oxidizing agents or bases. Ensure the storage area is well - ventilated to minimize exposure risks.
Shipping 3 - iodo - 2 - methylbenzoic acid is shipped in well - sealed, corrosion - resistant containers. Packaging follows chemical transportation regulations to prevent leakage, ensuring safe transit at ambient temperatures during shipping.
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3-iodo-2-methylbenzoic Acid 3-iodo-2-methylbenzoic Acid 3-iodo-2-methylbenzoic Acid
General Information
Frequently Asked Questions
What is the chemical structure of 3-iodo-2-methylbenzoic Acid?
3-Iodo-2-methylbenzoic acid is 3-iodo-2-methylbenzoic acid, and its chemical structure can be described as follows.
This compound belongs to a benzoic acid derivative. The structure of benzoic acid is that the benzene ring is connected to the carboxyl group (-COOH). On the basis of benzoic acid, 3-iodo-2-methylbenzoic acid is based on benzoic acid. A methyl (-CH 🥰) is added to the benzene ring at position 2, and an iodine atom (-I) is added at position 3.
The benzene ring is a six-membered ring structure, which is composed of six carbon atoms connected to each other by conjugated double bonds to form a planar structure. It has a unique aromaticity, and the electron cloud is evenly distributed above and below the ring, giving high stability to the benzene ring.
The carboxyl group is formed by connecting a carbonyl group (C = O) with a hydroxyl group (-OH). The carbon atom in the carbonyl group is connected to the oxygen atom by a double bond, and the oxygen atom in the hydroxyl group is connected to the carbon atom by a single bond. The carboxyl group is acidic. Due to the strong electronegativity of the oxygen atom in the hydroxyl group, the electron cloud of the hydrogen-oxygen bond is biased towards oxygen, and the hydrogen is easily dissociated in the form of protons. The methyl group at position
2 is an alkyl group obtained by removing one hydrogen atom from methane. It is a saturated structure, and the carbon is connected to the benzene ring carbon atom and three hydrogen atoms by a single bond. The existence of methyl groups has a certain electron
The iodine atom at position 3 is a halogen atom, which is connected to the carbon atom of the benzene ring by a single bond. The electronegativity of iodine atom is stronger than that of carbon atom, which will reduce the electron cloud density of the benzene ring and affect the chemical properties such as electrophilic substitution reactivity on the benzene ring.
In this way, 3-iodine-2-methylbenzoic acid exhibits unique chemical properties and reactivity due to the interaction of benzene ring, carboxyl group, methyl group and iodine atom
What are the main uses of 3-iodo-2-methylbenzoic Acid?
3-Iodine-2-methylbenzoic acid, this substance has a wide range of uses. In the field of pharmaceutical synthesis, it is often used as a key intermediate. Due to the structural properties of this compound, it can be converted into substances with specific pharmacological activities through many chemical reactions. For example, by combining with other organic molecules through appropriate reaction steps, therapeutic drugs for specific diseases can be created, or new drug molecular architectures can be developed, opening up new avenues for pharmaceutical research and development.
In the field of materials science, it also has its uses. Because it contains specific groups such as iodine and methyl, it gives materials unique properties. For example, it can be used to prepare materials with special optical or electrical properties. By introducing it into the structure of polymer materials, it can improve the electrical conductivity of materials, which makes the materials have potential applications in the field of electronic device manufacturing, such as in the synthesis of some new conductive polymers to improve device performance.
Furthermore, in organic synthesis chemistry, 3-iodine-2-methylbenzoic acid is an extremely important raw material. The synthesis of many complex organic compounds often starts with this. The presence of iodine atoms, carboxyl groups and methyl groups provides a variety of activity check points for organic reactions. Chemists can skillfully use these check points according to specific reaction requirements to carry out nucleophilic substitution, coupling reactions, etc., to construct various complex organic molecular structures, thereby enriching the types of organic compounds and promoting the development of organic synthetic chemistry.
What are the physical properties of 3-iodo-2-methylbenzoic Acid?
3-Iodo-2-methylbenzoic acid is also an organic compound. Its physical properties are quite important and are related to many chemical applications.
This compound is often in a solid state at room temperature. Due to the existence of various forces between molecules, it has a relatively stable solid structure. Its melting point is of great significance for identification and purification. Experiments have determined that the melting point is within a specific range. This value can help chemists control the conditions during operation to achieve accurate separation and purification.
In terms of its solubility, it shows certain characteristics in common organic solvents. In polar organic solvents such as ethanol and acetone, it has a certain solubility. Due to the fact that the molecule of the compound has a certain polarity, it can form intermolecular forces with polar solvents, such as hydrogen bonds, van der Waals forces, etc., so it can be partially dissolved. However, in non-polar solvents such as n-hexane, the solubility is very small, because the force between it and non-polar solvents is weak.
Furthermore, the density of 3-iodine-2-methylbenzoic acid is also a key physical property. Its density is different from that of water. This property has important guiding value when it involves operations such as liquid-liquid separation. Through density differences, suitable methods can be used to separate it from other substances.
In addition, the color state of the compound is also worthy of attention. Usually presented as a white to off-white solid, this appearance feature can provide an intuitive basis for preliminary identification. Chemists can preliminarily judge its purity and reaction process by observing the color and morphology during the experimental process.
In summary, the physical properties such as melting point, solubility, density and color state of 3-iodine-2-methylbenzoic acid play an indispensable role in many fields such as organic chemistry research, drug synthesis, material preparation, etc., providing an important reference for the design, implementation and monitoring of related operations and reactions.
What are the synthetic methods of 3-iodo-2-methylbenzoic Acid?
The synthesis method of 3-iodine-2-methylbenzoic acid has existed in ancient times, and has gradually become more diverse and complete with the changes of time. In the past, the synthesis of this compound often relied on the classical chemical path. Although complicated, it laid the foundation for the development of today.
First, 2-methylbenzoic acid is used as the starting material, and iodine atoms are added to the benzene ring by halogenation reaction. To perform this halogenation, a source of iodine, such as iodine elemental substance, is often used, supplemented by appropriate catalysts, such as iron trichloride, concentrated sulfuric acid, etc., to promote the reaction. During halogenation, the reaction conditions, such as temperature, reaction duration, and the proportion of reactants, must be carefully observed. If the temperature is too high, the side reactions may occur, and the product is impure; if the temperature is too low, the reaction will be delayed and the yield will not be high. In this process, the iodine atom preferentially adheres to the specific position of the benzene ring, which is determined by the localization effect of the original substituent on the benzene ring.
Second, there are also other aromatic derivatives as starting materials, which are converted into the target product through multiple steps. First, the aromatic hydrocarbon is methylated, a methyl group is introduced, and then a halogenation reaction is carried out to access the iodine atom. Finally, the specific functional group is converted into a carboxylic group through a carboxylation reaction, thereby obtaining 3-iodine-2-methylbenzoic acid. Although there are many steps in this path, the reaction selectivity of each step is controllable, and However, every step of the reaction requires fine operation, from the precise weighing of the reactants to the strict control of the reaction environment, all of which are critical to success or failure.
There are also those who use modern organic synthesis technologies, such as transition metal catalysis. Using transition metals such as palladium and copper as catalysts allows the reaction to proceed efficiently under milder conditions with excellent selectivity. Such methods not only reduce the reaction steps, but also improve the atomic economy, which is in line with the concept of green chemistry. However, transition metal catalysts are expensive, and the separation and recovery after use is also a challenge. They need to be properly disposed of to reduce costs and avoid pollution.
In summary, there are many methods for synthesizing 3-iodine-2-methylbenzoic acid, each with its own advantages and disadvantages. In practical applications, the appropriate synthesis path should be carefully selected according to specific requirements, such as product purity, cost, yield, and other factors.
What are the precautions for 3-iodo-2-methylbenzoic Acid in storage and transportation?
3-Iodine-2-methylbenzoic acid, this is an organic compound. When storing and transporting, many matters must be paid attention to.
First, let's talk about storage. First, choose a cool, dry and well-ventilated place. Because it is easily decomposed by heat, humid environment or deterioration, good ventilation can prevent the accumulation of harmful gases. Second, it must be stored separately from oxidants and alkalis. Oxidants are highly oxidizing, and contact with them may cause severe reactions. Alkalis and the acid can neutralize and react, damaging their quality. Third, the storage container must be tightly sealed. In this way, it can not only prevent volatilization, but also avoid reaction with components in the air such as moisture and oxygen. Fourth, clear warning signs should be set up, and the words "corrosive goods" should be written to remind others.
As for transportation, first of all, the packaging must be tight and stable. Use suitable packaging materials, such as corrosion-resistant plastic drums or glass bottles, and wrap cushioning materials to prevent packaging damage caused by transportation turbulence. Secondly, transport vehicles need to be equipped with good ventilation and anti-leakage devices. In the event of a leak, ventilation can reduce the concentration of harmful gases and prevent accidents from expanding; anti-leakage devices can prevent the spread of materials. In addition, transport personnel must be professionally trained and familiar with the characteristics of the chemical and emergency treatment methods. In case of emergencies such as leaks, they can respond quickly and correctly. Finally, the transportation process should strictly follow relevant regulations and standards, follow the designated route, and avoid sensitive areas such as crowded areas and water sources.