Methyl 5 Iodo 2 Methylbenzoate
Iodobenzene

Methyl 5 Iodo 2 Methylbenzoate

Fengxi Chemical

Specifications

HS Code

582081

Chemical Formula C9H9IO2
Molar Mass 278.07 g/mol
Appearance Solid (Typical appearance, exact may vary)
Melting Point Data may vary, specific value depends on purity etc.
Boiling Point Data may vary, related to purity and conditions
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Density Data may vary based on conditions and purity
Odor May have a characteristic organic odor
Flash Point Data may vary depending on experimental conditions
Chemical Formula C9H9IO2
Molar Mass 278.07 g/mol
Appearance Solid (usually)
Melting Point Data may vary, check literature
Boiling Point Data may vary, check literature
Solubility In Water Insoluble (likely, due to non - polar nature)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Density Data may vary, check literature
Flash Point Data may vary, check literature
Stability Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula C9H9IO2
Molar Mass 262.07 g/mol
Appearance Solid (likely white or off - white)
Melting Point Data needed
Boiling Point Data needed
Density Data needed
Solubility In Water Low solubility (organic ester, likely insoluble in water)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate
Flash Point Data needed
Vapor Pressure Low (as a solid at normal conditions)
Chemical Formula C9H9IO2
Molar Mass 262.07 g/mol
Appearance Solid (usually white to off - white)
Melting Point Typically in the range of 50 - 55 °C (approximate, may vary)
Density Estimated density around 1.7 - 1.8 g/cm³ (approximate)
Solubility In Water Insoluble in water
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate
Odor Odorless or very faint odor
Packing & Storage
Packing 100g of Methyl 5 - iodo - 2 - methylbenzoate packaged in a sealed glass bottle.
Storage Methyl 5 - iodo - 2 - methylbenzoate should be stored in a cool, dry, well - ventilated area, away from heat sources and ignition points. Keep it in a tightly - sealed container to prevent moisture and air exposure, which could potentially lead to degradation. Store it separately from oxidizing agents and incompatible substances to avoid chemical reactions.
Shipping Methyl 5 - iodo - 2 - methylbenzoate is shipped in well - sealed containers, compliant with chemical transport regulations. Shipment may involve temperature - controlled trucks to prevent degradation, ensuring safe delivery.
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Methyl 5 Iodo 2 Methylbenzoate Methyl 5 Iodo 2 Methylbenzoate Methyl 5 Iodo 2 Methylbenzoate
General Information
Frequently Asked Questions
What are the chemical properties of Methyl 5-iodo-2-methylbenzoate?
Methyl-5-iodine-2-methylbenzoate, this is an organic compound. Its chemical properties are unique and contain many interesting properties.
In this compound, the iodine atom coexists with the methyl and benzoate groups. The iodine atom is active, which makes the compound exhibit unique activities in many reactions. For example, it may participate in nucleophilic substitution reactions because the iodine atom can be replaced by other nucleophiles, which is an important means of organic synthesis.
Furthermore, the existence of two methyl groups has a significant impact on the molecular spatial structure and electron cloud distribution. Methyl groups are electron-supplying groups, which can change the electron density of the benzene ring, thereby affecting the reactivity and selectivity on the benzene ring.
Its ester group structure also has special chemical properties. The ester group can undergo hydrolysis reaction and decompose into corresponding carboxylic acids and alcohols under acidic or alkaline conditions. Hydrolysis under alkaline conditions is often referred to as saponification reaction. This process is of great significance for the preparation of carboxylic acids and related derivatives.
In addition, the compound is widely used in the field of organic synthesis, or as a key intermediate, participating in the construction of complex organic molecules. Due to its unique structure and reactivity, it can provide a basis for the synthesis of compounds with specific functions and structures, enabling chemists to create more new and valuable organic materials.
What are the synthetic methods of Methyl 5-iodo-2-methylbenzoate?
There are several common methods for synthesizing methyl 5-iodine-2-methylbenzoate.
First, it can be started from 2-methylbenzoic acid. First, 2-methylbenzoic acid is mixed with methanol, and a strong acid such as concentrated sulfuric acid is used as a catalyst, and an esterification reaction is carried out by heating to form methyl 2-methylbenzoate. This reaction is based on the principle of dehydration of carboxylic acid and alcohol under acid catalysis to form esters. Then, methyl 2-methylbenzoate is iodized. Elemental iodine and an appropriate oxidant, such as hydrogen peroxide, can be used in a suitable solvent, such as glacial acetic acid, at a suitable temperature. This iodization step is to activate the iodine elemental substance with an oxidizing agent, and then undergo an electrophilic substitution reaction with the benzene ring, introducing iodine atoms at a specific position in the benzene ring, and finally obtaining methyl 5-iodine-2-methylbenzoate.
Second, we can also start from 2-methyl-5-nitrobenzoic acid. First, with suitable reducing agents, such as iron and hydrochloric acid, the nitro group is reduced to amino group to obtain 2-methyl-5-aminobenzoic acid. Subsequently, 2-methyl-5-aminobenzoic acid is diazotized with sodium nitrite and hydrochloric acid at low temperature to form a diazonium salt. Then, the diazonium salt is reacted with potassium iodide solution, and the diazonium group is replaced by iodine atom to obtain 5-iodine-2-methylbenzoic acid. Finally, 5-iodine-2-methylbenzoic acid is esterified with methanol under acid catalysis to obtain the target product methyl 5-iodine-2-methylbenzoate. This route is a multi-step reaction, using the characteristics and reactions of different functional groups to gradually construct the target molecular structure.
Furthermore, you can also try to use 2-methyl-5-halobenzoic acid methyl ester as raw material (the halogenated group can be chlorine, bromine, etc.). Methyl 5-iodo-2-methylbenzoate is synthesized by a halogen exchange reaction in which halogen atoms are replaced with iodide reagents, such as sodium iodide, in appropriate solvents and conditions. This method is relatively direct, and the preparation of the target product is achieved by means of the selectivity and high efficiency of the halogen exchange reaction.
Different synthesis methods have their own advantages and disadvantages, and the most suitable method should be selected according to the actual situation, such as the availability of raw materials, the difficulty of reaction conditions, and the cost.
Where is Methyl 5-iodo-2-methylbenzoate used?
Methyl-5-iodine-2-methylbenzoate, an organic compound. It has applications in many fields, and let me tell you one by one.
In the field of medicinal chemistry, such iodine-containing organic compounds may be used as important intermediates. Due to the unique chemical properties of iodine atoms, they can significantly affect molecular activity and reactivity. Through specific chemical reactions, they can be converted into drug molecules with specific pharmacological activities. For example, they can be used to synthesize inhibitors targeting certain disease targets, by precisely regulating relevant signaling pathways in organisms, for the purpose of treating diseases.
In the field of materials science, methyl-5-iodine-2-methylbenzoate also has its uses. It may participate in the preparation of functional polymer materials. In the polymerization reaction, as a monomer or modifier, it can endow polymer materials with unique properties, such as improving the optical and electrical properties of materials. For example, when preparing polymer materials used in optoelectronic devices, the introduction of this compound may optimize the absorption and emission characteristics of materials to light and improve the efficiency of optoelectronic devices.
Furthermore, in the field of organic synthesis chemistry, it is often used as a key building block. Because its structure contains both ester groups, iodine atoms and methyl groups, it can provide a variety of reaction check points for organic synthesis. Chemists can use this to build more complex organic molecular structures, achieve the synthesis of various target compounds, greatly enrich the variety and structural diversity of organic compounds, and promote the development of organic synthetic chemistry.
What are the physical properties of Methyl 5-iodo-2-methylbenzoate?
Methyl-5-iodine-2-methylbenzoate is also an organic compound. Its physical properties are quite important, and today I will give you a detailed look.
Looking at its properties, under normal temperature and pressure, this substance is often in a solid state. The value of its melting point is actually the key physical property. The melting point of methyl-5-iodine-2-methylbenzoate is also the temperature limit for the transformation of a substance from a solid state to a liquid state. The melting point of methyl-5-iodine-2-methylbenzoate is specific and accurate, which can be used to identify this substance, and is also of great significance in the process of separation and purification.
Furthermore, the boiling point cannot be ignored. The boiling point is the temperature at which a substance changes from a liquid state to a gas state under a specific pressure. The boiling point of this compound determines its volatilization characteristics under heating conditions, and has reference value in many fields such as chemical production and experimental operation.
In terms of solubility, this compound behaves differently in different solvents. In organic solvents such as ethanol, ether, etc., or exhibit certain solubility. The polarity and molecular structure of organic solvents interact with methyl-5-iodine-2-methylbenzoate, resulting in different degrees of solubility. In water, due to its structure, the solubility is poor. Water is a polar solvent, and the interaction force with this compound is weak, so it is difficult to dissolve.
Density is also one of its important physical properties. The density is also the mass of the substance per unit volume. The density of methyl-5-iodine-2-methylbenzoate is related to its distribution in the mixed system, and has an impact on chemical process design, fluid transportation, etc.
In addition, the color state of this substance also needs to be paid attention to. Under normal circumstances, it may be a white to off-white solid, and this color state characteristic can be used for preliminary identification.
In summary, the melting point, boiling point, solubility, density and color state of methyl-5-iodine-2-methylbenzoate are of great significance in chemical research, industrial production and many other aspects. It is also the basis for in-depth understanding and application of this substance.
What is the market outlook for Methyl 5-iodo-2-methylbenzoate?
Methyl-5-iodine-2-methylbenzoate is worth exploring in today's market prospects. It has a wide range of uses in the field of organic synthesis.
Gein organic synthesis often requires the introduction of specific functional groups to construct complex molecules. The combination of iodine atoms, ester groups and methyl groups in methyl-5-iodine-2-methylbenzoate makes it a key intermediate. It can interact with other reagents through many chemical reactions, such as nucleophilic substitution, coupling reactions, etc., to form various novel organic compounds, which are in potential demand in medicine, materials and other industries.
Looking at the pharmaceutical industry, the demand for organic molecules with diverse structures is increasing in the research and development of new drugs. Methyl-5-iodine-2-methylbenzoate can be used as a starting material. After chemical modification, compounds with biological activity can be derived, which is expected to become new drugs.
As for the field of materials, with the development of advanced materials, the demand for special structure organic molecules also increases. This compound may be used to prepare functional polymer materials, optoelectronic materials, etc., giving the material unique electrical and optical properties.
However, its market prospects are also constrained by several factors. The first one to bear the brunt is the cost of synthesis. If the synthesis process is complicated and the raw materials are expensive, its large-scale application is limited. Furthermore, regulations and regulations. In medicine and materials applications, it is necessary to meet strict regulatory standards, and testing and approval are time-consuming and laborious.
Despite this, with the advancement of science and technology, the synthesis process or optimization, the cost is reduced; at the same time, the improvement of the regulatory system also provides a guarantee for orderly development. With the market prospect of methyl-5-iodine-2-methylbenzoate, although challenges coexist, there are also abundant opportunities. It is expected to emerge in the future organic synthesis-related industries and open up a wide range of fields.