Methyl 2 Iodo 5 Methylbenzoate
Iodobenzene

Methyl 2 Iodo 5 Methylbenzoate

Fengxi Chemical

Specifications

HS Code

809175

Chemical Formula C9H9IO2
Molar Mass 262.07 g/mol
Appearance Solid (usually)
Physical State At Room Temp Solid
Boiling Point Data may vary, around 300°C (estimated based on similar compounds)
Melting Point Data may vary, around 50 - 60°C (estimated)
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Density Data may vary, but likely around 1.7 - 1.8 g/cm³ (estimated)
Flash Point Data may vary, around 130 - 140°C (estimated)
Hazard Class Irritant (may cause skin, eye, and respiratory irritation)
Chemical Formula C9H9IO2
Molar Mass 262.07 g/mol
Appearance Typically a solid (description may vary)
Melting Point Data specific to the compound needed
Boiling Point Data specific to the compound needed
Solubility In Water Low (organic compound, likely sparingly soluble)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Density Data specific to the compound needed
Flash Point Data specific to the compound needed
Purity Usually Varies by source, e.g., 95%+ in high - quality samples
Chemical Formula C9H9IO2
Molar Mass 262.07 g/mol
Appearance Solid (presumably, based on similar compounds)
Physical State At Room Temperature Solid
Solubility In Water Insoluble (expected due to non - polar nature of aromatic ring and ester group)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, etc.
Iodine Containing Functional Group Reactivity Iodo group is reactive in substitution reactions
Chemical Formula C9H9IO2
Molar Mass 262.07 g/mol
Appearance Solid (likely white or off - white)
Melting Point Data needed from literature
Boiling Point Data needed from literature
Solubility In Water Insoluble (hydrophobic due to non - polar aromatic and alkyl groups)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Density Data needed from literature
Flash Point Data needed from literature
Stability Stable under normal conditions, but iodine can be reactive in certain reactions
Packing & Storage
Packing 100g of Methyl 2 - iodo - 5 - methylbenzoate packaged in a sealed glass bottle.
Storage Methyl 2 - iodo - 5 - methylbenzoate should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. It should be kept in a tightly sealed container to prevent exposure to air and moisture, which could potentially lead to decomposition. Store it separately from incompatible substances like strong oxidizing agents and bases.
Shipping Methyl 2 - iodo - 5 - methylbenzoate is shipped in properly sealed, corrosion - resistant containers. Packaging adheres to chemical transport regulations. Shipment is handled with care to prevent breakage and ensure safe transit.
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Methyl 2 Iodo 5 Methylbenzoate Methyl 2 Iodo 5 Methylbenzoate Methyl 2 Iodo 5 Methylbenzoate
General Information
Frequently Asked Questions
What are the chemical properties of Methyl 2-iodo-5-methylbenzoate?
Methyl 2-iodine-5-methylbenzoate, this is an organic compound. Its chemical properties are unique, let me explain in detail.
First of all, the iodine atom is quite active. This compound can also occur in typical reactions of halogenated hydrocarbons. For example, nucleophilic substitution reactions, iodine atoms can be replaced by many nucleophilic reagents. Because iodine atoms are used as leaving groups, the tendency to leave is quite large, making the compound easy to react with nucleophilic reagents containing hydroxyl groups and amino groups under appropriate conditions to form new compounds.
In addition, ester groups also have important chemical properties. Esters can undergo hydrolysis reactions under acidic or basic conditions. Under acidic conditions, the corresponding carboxylic acids and alcohols are hydrolyzed; under alkaline conditions, the hydrolysis is more thorough, resulting in carboxylic salts and alcohols. The ester group of methyl 2-iodine-5-methylbenzoate follows the general law in such hydrolysis reactions.
In addition, although the methyl group on the benzene ring is relatively stable, it can also participate in the reaction under certain conditions. For example, under the action of strong oxidants, methyl groups can be oxidized to carboxyl groups. In addition, the presence of benzene rings allows the compound to undergo typical reactions of aromatic hydrocarbons, such as electrophilic substitution reactions. Due to the high density of electron clouds in the benzene ring, it is vulnerable to attack by electrophilic reagents, and reactions such as nitrification and halogenation In short, the iodine atom of methyl 2-iodine-5-methylbenzoate, the ester group and the methyl group on the benzene ring endow it with diverse chemical properties, which can be used as an important intermediate in the field of organic synthesis and participate in the preparation of many organic compounds.
What is the synthesis method of Methyl 2-iodo-5-methylbenzoate?
To prepare methyl 2-iodine-5-methylbenzoate, the following method can be followed.
First, 5-methylbenzoic acid is used as the starting material. Mix it with methanol, add an appropriate amount of concentrated sulfuric acid as the catalyst, and heat up to carry out the esterification reaction. This process needs to be controlled at a suitable temperature range and stirred from time to time to make the reaction sufficient. The chemical reaction formula is as follows: 5-methylbenzoic acid + methanol $\ xrightarrow [] {concentrated sulfuric acid} $methyl 5-methylbenzoate + water. After the reaction is completed, pure methyl 5-methylbenzoate is obtained through neutralization, separation, distillation and other steps.
Then, methyl 5-methylbenzoate is iodized with iodine. Usually iodine is combined with an appropriate amount of oxidant, such as hydrogen peroxide or potassium persulfate. In a suitable solvent, such as dichloromethane or chloroform, the reaction is stirred at a controlled temperature. The amount of oxidant, reaction temperature and time are all critical. For example, taking hydrogen peroxide as an example, the chemical reaction formula is roughly: methyl 5-methylbenzoate + iodine + hydrogen peroxide $\ xrightarrow [] {solvent} $methyl 2-iodine-5-methylbenzoate + other products (e.g. water may be formed, etc.). After the reaction, the product was purified by extraction, washing, drying and column chromatography to obtain the target product methyl 2-iodine-5-methylbenzoate.
In this synthesis method, the conditions of each step need to be carefully adjusted to improve the purity and yield of the product.
Where is Methyl 2-iodo-5-methylbenzoate used?
Methyl-2-iodine-5-methylbenzoate is widely used in the field of organic synthesis. This compound has a unique structure, in which the iodine atom coexists with the ester group and methyl group, giving it specific chemical activity.
In the field of pharmaceutical chemistry, it is often a key intermediate for the synthesis of biologically active molecules. Because its structure can be modified by various chemical reactions, such as nucleophilic substitution reactions, iodine atoms can be replaced by other functional groups, thereby constructing a complex drug molecular skeleton, providing the possibility for the development of new drugs.
In the field of materials science, it may also have its uses. Due to its chemical properties, it can affect the properties of materials, such as polymerization with other compounds, which can change the solubility and stability of materials, or be used to prepare polymer materials with specific properties.
Furthermore, in the fragrance industry, it can be used as a starting material for synthesizing fragrances. By modifying its structure, compounds with special aromas can be generated, enriching the types of fragrances and meeting different needs. In short, methyl-2-iodine-5-methylbenzoate has potential application value in various fields and can provide assistance for the development of various fields.
What are the physical properties of Methyl 2-iodo-5-methylbenzoate?
Methyl-2-iodine-5-methylbenzoate is one of the organic compounds. Its physical properties are described in detail as follows.
Looking at its properties, at room temperature, it is mostly in a solid state, which is relatively stable due to intermolecular forces. Its melting point is quite characteristic, the melting point is about [X] ° C, and the boiling point is about [X] ° C. The melting point is the temperature at which a substance changes from a solid state to a liquid state. The melting point of this compound reflects the strength of its intermolecular bonding. The boiling point is the temperature at which a liquid turns into a gas, indicating the energy required to overcome the intermolecular forces to gasify the substance.
As for solubility, this compound has good solubility in organic solvents such as ethanol and ether. Due to the principle of "similar miscibility", its organic structure is similar to the molecular structure of organic solvents, and the intermolecular forces can interact, so it can be dissolved. However, in water, the solubility is poor. Water is a highly polar solvent, while methyl-2-iodine-5-methylbenzoate has a weak polarity, and it is difficult to form an effective force between the two molecules, making it difficult to dissolve in water.
Its density is also an important physical property, about [X] g/cm ³, which is slightly higher than that of water. This reflects the density of molecules. The value of density is affected by the molecular mass and the arrangement of molecules.
In addition, its appearance may be white to light yellow, and the formation of this color is related to factors such as electron transition in the molecular structure. When light is irradiated, the electrons in the molecule absorb light of a specific wavelength and transition, and the rest of the wavelengths are reflected, resulting in corresponding colors.
In summary, the physical properties of methyl-2-iodine-5-methylbenzoate, such as its properties, melting point, solubility, density, appearance color, etc., are determined by its molecular structure, and the properties are interrelated, which is of great significance in the research and application of organic chemistry.
What is the market outlook for Methyl 2-iodo-5-methylbenzoate?
Methyl-2-iodine-5-methylbenzoate, this substance is in the market and has a promising future. It is widely used in the field of organic synthesis. It can be used as a key intermediate to prepare many high-value-added fine chemicals.
In the process of pharmaceutical research and development, it may be able to participate in the creation of new drugs. With the vigorous development of the pharmaceutical industry, the demand for characteristic intermediates is increasing. It is expected to add bricks to the research and development of new drugs with its unique structure, thus gaining a considerable market share.
In the field of materials science, it also has potential applications. It may be used to synthesize special polymer materials, giving materials unique properties, such as excellent optical and electrical properties. With the continuous innovation of materials science, the exploration of new functional materials is not limited. As a potential raw material, it may find a place in the emerging materials market.
However, its market also faces challenges. The synthesis process may be complex and costly, which restricts large-scale production and wide application. Furthermore, similar alternatives may already be available in the market, and the competition is quite fierce. To expand the market, it is necessary to improve the synthesis process, reduce costs and increase efficiency, and enhance product competitiveness. Only in this way can methyl-2-iodine-5-methylbenzoate gain a firm foothold in the market and open up broad prospects.