Methyl Chloro 5 Iodobenzoate
Iodobenzene

Methyl -chloro-5-iodobenzoate

Fengxi Chemical

Specifications

HS Code

237035

Name Methyl 2 - chloro - 5 - iodobenzoate
Molecular Formula C8H6ClIO2
Molecular Weight 296.49
Appearance Solid (likely white or off - white)
Melting Point Data needed
Boiling Point Data needed
Density Data needed
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Flash Point Data needed
Purity Typically specified as a percentage (e.g., 95%, 98% etc.)
Name Methyl 5 - chloro - 5 - iodobenzoate
Molecular Formula C8H6ClIO2
Molar Mass 300.49 g/mol
Appearance Solid (usually)
Solubility In Water Low (organic compound, relatively non - polar)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Chemical Stability Stable under normal conditions, but can react with strong oxidizing and reducing agents
Name Methyl 5 - chloro - 5 - iodobenzoate
Chemical Formula C8H6ClIO2
Molar Mass 296.49 g/mol
Appearance Solid (predicted, actual may vary)
Melting Point Data needed
Boiling Point Data needed
Density Data needed
Solubility In Water Low (organic ester, likely sparingly soluble)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Flash Point Data needed
Hazard Class Data needed
Stability Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula C8H6ClIO2
Molecular Weight 282.49
Appearance Solid (predicted)
Boiling Point Estimated around 300 - 350 °C (under normal pressure, estimated)
Melting Point No common data (but should be solid at room temperature based on structure)
Density No standard data, but predicted to be heavier than water considering iodine and chlorine
Solubility In Water Low solubility, due to non - polar benzene ring and ester group
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, etc.
Flash Point Estimated high flash point as it's a relatively high - molecular - weight and non - volatile compound
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
Packing & Storage
Packing 100g of Methyl -chloro -5 -iodobenzoate in a sealed, labeled chemical - grade bottle.
Storage Methyl -chloro -5 -iodobenzoate should be stored in a cool, dry, well -ventilated area, away from heat sources and direct sunlight. Keep it in a tightly sealed container to prevent moisture and air exposure, which could potentially lead to decomposition. Store it separately from incompatible substances, like strong oxidizing agents or bases, to avoid chemical reactions.
Shipping Methyl -chloro -5 -iodobenzoate, a chemical, is shipped in accordance with strict hazardous material regulations. Packed in suitable containers, it's transported via approved carriers, ensuring safety during transit.
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Methyl -chloro-5-iodobenzoate Methyl -chloro-5-iodobenzoate Methyl -chloro-5-iodobenzoate
General Information
Frequently Asked Questions
What are the chemical properties of Methyl -chloro-5-iodobenzoate?
Methyl-chloro-5-iodobenzoate (methyl-chloro-5-iodobenzoate) is an organic compound. Its chemical properties are particularly important and are closely related to many organic reactions.
In this compound, chlorine (Cl) and iodine (I) are halogen atoms, which have unique reactivity. Halogen atoms can undergo nucleophilic substitution reactions. When encountering nucleophiles, halogen atoms can be replaced. For example, under basic conditions, hydroxyl (OH) and other nucleophiles can attack carbon atoms connected to halogen atoms, and the halogen atoms leave to form corresponding substitutions. This reaction is often used in organic synthesis to introduce new functional groups, laying the foundation for the construction of complex organic molecules.
Its ester groups (-COOCH
) also have significant chemical properties. The ester groups can undergo hydrolysis, and ester bonds can be broken in acidic or alkaline environments. In acidic hydrolysis, benzoic acid and methanol are formed, and the reaction is reversible; in alkaline hydrolysis, benzoate and methanol are formed more thoroughly. This process is widely used in the preparation and analysis of organic chemistry, and can be used to prepare specific carboxylic acids or alcohols.
In addition, Methyl-chloro-5-iodobenzoate can participate in aromatic ring-related reactions due to the presence of aromatic ring structures in the molecule. For example, under the action of appropriate catalysts, electrophilic substitution reactions on aromatic rings can occur. Halogen atoms and ester groups will have a positioning effect on the reaction check point, affecting the position of electrophilic reagents attacking aromatic rings, and then synthesizing derivatives with different substitution modes. It is of great significance in the fields of medicinal chemistry and materials science, and helps to create new functional materials or pharmaceutical active ingredients.
In summary, Methyl-chloro-5-iodobenzoate exhibits rich and diverse chemical properties due to the structure of halogen atoms, ester groups and aromatic rings, and plays a key role in organic synthesis and related fields, providing a broad space for organic chemistry research and application.
What are the common synthesis methods of Methyl -chloro-5-iodobenzoate?
The common synthesis method of Methyl-chloro-5-iodobenzoate (methyl-chloro-5-iodobenzoate) is an important matter for chemical preparation. One method can also be started by benzoic acid derivatives. First, benzoic acid is halogenated, and specific halogenated reagents, such as chlorine and iodine-containing reagents, are introduced into chlorine atoms and iodine atoms at designated positions in the benzene ring under suitable reaction conditions, such as specific temperatures and catalysts, to obtain chloro-5-iodobenzoate. Thereafter, the product is esterified with methanol under the catalysis of acid. Sulfuric acid is often used as a catalyst, and heating prompts the reaction to occur, and then methyl-chloro-5-iodobenzoate is obtained.
Another method can be started from halogenated benzene. Using suitable halogenated benzene as raw material, through Fu-Ke acylation reaction, carboxyl related groups are introduced, and then through halogenation step, chlorine and iodine atoms are introduced, and finally esterified with methanol to obtain the target product. In this process, the Fu-Ke acylation reaction needs to select suitable acylating reagents and catalysts, and the halogenation reaction also needs to precisely control the conditions to achieve the desired substitution position and reaction yield.
Another approach can be started from benzaldehyde derivatives containing iodine or chlorine. The aldehyde group is first converted into carboxyl group by suitable oxidation reaction, and then esterified into ester, and then another halogen atom is introduced at a specific position on the benzene ring to synthesize methyl-chloro-5-iodobenzoate. Appropriate oxidizing agents can be selected for the oxidation reaction, and the esterification and halogenation steps must also follow the corresponding reaction laws and conditions.
Where is Methyl -chloro-5-iodobenzoate used?
Methyl-chloro-5-iodobenzoate is used in various fields.
In the field of pharmaceutical research and development, this compound can be a key intermediate. Due to the characteristics of halogen atoms and ester groups in its structure, organic synthesis can be used to react with many reagents to construct complex molecules with biological activity. Chemists can create novel drug molecules with their delicate designs to deal with various diseases, such as the development of anti-cancer drugs, or can use their unique structure to modify and modify them to obtain new anti-cancer drugs with good targeting and excellent efficacy.
In the field of materials science, methyl-chloro-5-iodobenzoate also has potential. Because it contains specific functional groups, it can participate in the synthesis of polymer materials. For example, the preparation of special plastics, by introducing special structural fragments, endows the material with unique properties such as excellent heat resistance and chemical corrosion resistance, and then expands the application of the material in high-end fields such as aerospace and electronic devices.
Furthermore, in the fine chemical industry, this substance can be used as a raw material for special chemicals. After a series of reactions, it is made into special fragrances, dyes or additives. For example, in the manufacture of dyes, using its structural characteristics, new dyes with bright color and high stability can be synthesized to meet the needs of high-quality dyes in textile, printing and other industries.
To sum up, methyl-chloro-5-iodobenzoate, with its unique structure, has shown broad application prospects in the fields of medicine, materials, and fine chemicals, providing an important chemical raw material basis for innovation and development in related fields.
What are the physical properties of Methyl -chloro-5-iodobenzoate?
Methyl-chloro-5-iodobenzoate is a kind of organic compound. Its physical properties are quite specific and have unique properties. Looking at its shape, at room temperature, it is mostly in a solid state, and the texture is relatively solid. Its color may be colorless to slightly yellow, just like the shimmer of the early morning light, elegant and clear.
When it comes to the melting point, it is about a specific temperature range. This temperature value is crucial for determining its purity and characteristics. When heated to the melting point, this material is like ice and snow when it is warm, gradually melting from solid to liquid, and its fluidity increases. Its boiling point is also a key physical property. Under specific pressure conditions, when heated to this temperature, the compound will turn into a gaseous state and rise.
As for solubility, in organic solvents, its performance varies. For example, in some polar organic solvents, fish-like water can be better dissolved to form a uniform solution; however, in water, it is like oil and water are incompatible, with little solubility and only a very small amount of dispersion.
In terms of density, it is larger than water. If it is placed in the same place as water, it will be like a stone sinking to the bottom and slowly settling to the bottom. In addition, this object may have a certain smell. Although it is not strong and pungent, it also has a unique smell, which can be used as one of the identification aids. Its various physical properties are of great significance in many fields such as organic synthesis and chemical analysis, laying an important foundation for related research and applications.
What is the market price of Methyl -chloro-5-iodobenzoate?
I think what you are asking is about the market price of "Methyl-chloro-5-iodobenzoate". However, this is not an easy matter, and the price of this compound often varies due to various factors.
First, the price of the raw material is the key factor. If the starting material required for the preparation of this "Methyl-chloro-5-iodobenzoate" is scarce, or its production is difficult, resulting in a high price of raw materials, the price of "Methyl-chloro-5-iodobenzoate" will also be high. If the starting material requires special excavation or complex synthesis, the cost will increase, which will eventually lead to an increase in the price of the product.
Second, the preparation process is complicated and simple, which also affects the price. If the preparation of this compound requires precise instruments, harsh reaction conditions, such as high temperature, high pressure, special catalysts, etc., and the process steps are cumbersome, multiple purification, separation and other operations are required, and manpower and material resources are expensive, then its price is not low.
Third, the supply and demand of the market determines the price. If the market has strong demand for this "Methyl-chloro-5-iodobenzoate", such as for specific drug research and development, high-end material synthesis and other fields, but the supply is limited, the supply will exceed the demand, and the price will rise; conversely, if the supply exceeds the demand, the price may drop.
Fourth, the scale of production is also relevant. In large-scale production, due to the scale effect, the unit cost may be reduced and the price may be more affordable; if small batch production, the cost sharing is high, and the price is relatively high.
And different suppliers sell "Methyl-chloro-5-iodobenzoate" at different prices due to differences in their own cost control and technical advantages. Therefore, in order to know the exact market price, it is necessary to carefully review the raw material market, production process, supply and demand situation, and the quotations of each supplier, and comprehensively consider to obtain a more accurate price.