4 Iodo 1 Tritylimidazole
Iodobenzene

4 Iodo 1 Tritylimidazole

Fengxi Chemical

Specifications

HS Code

837560

Chemical Formula C22H17IN2
Molecular Weight 434.29
Appearance Solid
Melting Point 147 - 151 °C
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Iodine Content High iodine content due to iodo - group
Trityl Group Characteristic Trityl group provides steric hindrance
Imidazole Ring Property Imidazole ring is reactive in some organic reactions
Stability Relatively stable under normal conditions
Color Typically colorless to light - colored solid
Chemical Formula C22H17IN2
Molecular Weight 434.29
Appearance Solid (Typical)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
Iodine Content Contains iodine atom crucial for certain reactions
Imidazole Ring Presence Has an imidazole ring which can participate in coordination chemistry
Trityl Group Attached Trityl group provides steric hindrance
Crystal Structure General Crystalline solid with ordered molecular packing
Thermal Stability Stable under normal storage conditions but may decompose upon heating
Reactivity Towards Nucleophiles Can react with nucleophiles at the iodine or imidazole sites
Chemical Formula C22H17IN2
Molecular Weight 434.29
Appearance Solid (Typical)
Melting Point 157 - 161 °C
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
Iodine Content High due to the iodo - group
Imidazole Ring Reactivity Reactive at the imidazole ring positions
Trityl Group Property Provides steric hindrance
Color Typically white to off - white
Stability Stable under normal storage conditions away from light and moisture
Chemical Formula C22H17IN2
Molecular Weight 434.29
Appearance Solid
Color Typically white to off - white
Melting Point 165 - 168 °C
Solubility Soluble in some organic solvents like dichloromethane
Purity High - purity grades are often 95%+
Iodine Content Contributes to its reactivity due to iodine atom
Imidazole Based Structure Provides basic and coordinating properties
Trityl Group Influences steric and electronic properties
Packing & Storage
Packing 10 - gram vial of 4 - iodo - 1 - tritylimidazole, well - sealed in a chemical - resistant package.
Storage 4 - iodo - 1 - tritylimidazole should be stored in a cool, dry place away from heat sources and direct sunlight. Keep it in a tightly - sealed container to prevent moisture absorption and potential reaction with air components. Store in a well - ventilated area, separate from incompatible substances like strong oxidizing agents to avoid hazardous reactions.
Shipping 4 - iodo - 1 - tritylimidazole is shipped with careful packaging to prevent breakage. It's handled in accordance with chemical shipping regulations, ensuring proper containment and safety during transit to its destination.
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4-iodo-1-tritylimidazole 4-iodo-1-tritylimidazole 4-iodo-1-tritylimidazole
General Information
Frequently Asked Questions
What is the chemical structure of 4-iodo-1-tritylimidazole?
4-Iodo-1-tritylimidazole is one of the organic compounds. Its chemical structure is unique. In this compound, the imidazole ring is the core structure, and the imidazole ring is a five-membered heterocycle containing two nitrogen atoms. It is aromatic and is very important in many organic reactions and biological activity related studies.
In the first position of the imidazole ring, there is a triphenyl group connected. Triphenyl is formed by connecting three phenyl groups to a central carbon atom. Its large volume has a significant impact on the spatial structure and chemical properties of the molecule, often enhancing the stability of the molecule, and also affecting its solubility and reactivity.
In the fourth position of the imidazole ring, the iodine atom is connected. The iodine atom has a large atomic radius and electronegativity, and its introduction can change the electron cloud distribution of the molecule, affecting the polarity and chemical reactivity of the molecule. Iodine atoms are often important functional groups in organic synthesis and can participate in various reactions, such as coupling reactions, etc., providing the possibility to construct more complex organic molecular structures.
In this way, the chemical structure of 4-iodo-1-tritylimidazole, through the combination of imidazole ring, triphenyl and iodine atoms, endows it with unique physical and chemical properties, and occupies a place in the research and application of organic chemistry.
What are the main uses of 4-iodo-1-tritylimidazole?
4-Iodo-1-tritylimidazole is also a chemical substance. Its use is not limited, and it has many uses in the field of synthesis.
One of them, in the synthesis of chemical substances, is often used as a medium. Because of its unique properties, it can create multiple reactions, which can help the specific shape of chemical molecules. With its iodine atom and triphenylmethylimidazolyl properties, it can build the molecular framework required for chemical activity from even reactions, etc.
Second, in the field of materials science, it also has extraordinary performance. It can make some functional materials. For example, in the synthesis of optical materials, it can influence the sub-cloud composition and molecular arrangement of the material, and control the optical properties of the material, such as performance, light absorption and emission characteristics, etc., to help develop better optical materials.
Third, in the field of chemical research, 4-iodo-1-tritylimidazole can be used as a model compound. Because of its clarity and special inverse properties, studying its inverse process can provide insight into the principle of inverse, clarify the law of generation of cracking, and improve the improvement of chemical processing. In short, this compound has important values in various fields, and promotes the development of each field.
What are 4-iodo-1-tritylimidazole synthesis methods?
The synthesis method of 4-iodine-1-triphenylmethylimidazole has been known for a long time. A common method is to use imidazole as the starting material. Imidazole has active nitrogen atoms and can react with triphenylmethyl chloride under appropriate reaction conditions, such as in organic solvents. Under the catalysis of bases, the two interact and react through nucleophilic substitution to generate 1-triphenylmethylimidazole. This step requires attention to the control of reaction temperature, amount of base and reaction time. Too high or too low temperature and inappropriate amount of base may affect the yield and purity of the reaction.
Then, 1-triphenylmethylimidazole is further reacted with the iodine source. Commonly used iodine sources such as iodine elemental substance, under appropriate oxidation reagents and reaction conditions, iodization reaction occurs at a specific position on the benzene ring, and then 4-iodine-1-triphenylmethylimidazole is obtained. In this iodization step, the choice of oxidation reagent and the nature of the reaction solvent have a great influence on the selectivity and efficiency of the reaction.
There are also other methods, starting with benzene derivatives containing specific substituents, through multi-step reactions, imidazolyl and triphenylmethyl groups are gradually introduced, and finally the synthesis of 4-iodine-1-triphenylmethylimidazole is achieved. However, there are many steps in this approach, and each step needs to be carefully controlled to ensure the purity and yield of the product. Each step of the reaction requires careful operation according to the characteristics of the reactants and the differences in reaction conditions, in order to successfully synthesize the target product 4-iodine-1-triphenylmethylimidazole.
What are the physical properties of 4-iodo-1-tritylimidazole?
The 4-iodo-1-tritylimidazole is also an organic compound. Its physical properties are very important, and it is related to its performance in various chemical processes.
First of all, its appearance is usually a solid state, which is easy to store and operate. Its color may be white to off-white, and this pure color also reflects its high purity.
Melting point is a key item. Its melting point is in a specific temperature range, which gives it a specific phase transition property. When the temperature rises to the melting point, the compound changes from solid to liquid. This property can be used for purification and separation in many synthesis steps, and it can be precisely separated from the mixture by the difference in melting point.
In terms of solubility, 4-iodo-1-tritylimidazole exhibits good solubility in specific organic solvents. Such as common polar organic solvents, such as dichloromethane, N, N-dimethylformamide, etc., can be mutually soluble with it. This solubility property allows chemists to easily carry out various chemical reactions in solutions, providing the possibility for the synthesis of more complex organic molecules.
Furthermore, its density is also an important physical property. Although the specific value of its density varies slightly with conditions, it is roughly within a certain range. This density data provides accurate quantitative basis for solution preparation, reaction material measurement, etc.
In addition, the stability of this compound also belongs to the category of physical properties. Under normal environmental conditions, it has a certain stability, and it may encounter extreme conditions such as specific chemical reagents, light or high temperature, or undergo chemical changes. This stability consideration is particularly critical when storing and using the compound.
The physical properties of 4-iodo-1-tritylimidazole, such as appearance, melting point, solubility, density, and stability, are interrelated to form the basis of its chemical behavior and provide a solid physical basis for the research and application of organic synthetic chemistry.
What do 4-iodo-1-tritylimidazole need to pay attention to when storing and transporting?
4-Iodo-1-tritylimidazole is a special organic compound. When storing and transporting, it is necessary to pay attention to many key points.
Bearing the brunt, temperature control is crucial. This compound is quite sensitive to temperature, and high temperature can easily cause it to decompose and deteriorate, so it is best to store it in a cool place. Generally speaking, a low temperature environment of 0-10 degrees Celsius is preferred. When transporting, cold chain conditions should also be ensured to prevent temperature fluctuations from damaging its structure and properties.
Furthermore, the impact of humidity should not be underestimated. It is prone to moisture, and humid environments can cause adverse reactions such as hydrolysis. Therefore, when storing, it should be placed in a dry place, which can be matched with a desiccant to maintain a dry environment. During transportation, the packaging must have good moisture resistance to prevent the intrusion of external moisture.
Light is also a key factor. This compound is prone to photochemical reactions when exposed to light, which can change its chemical properties. Therefore, storage should be selected in a dark place, and it is better to hold it in a brown bottle. When transporting, the packaging should also be shaded to prevent light from affecting its quality.
In addition, the firmness of the packaging cannot be ignored. Due to its special chemical properties, if the packaging is damaged, it may not only cause the compound to leak, but also react with external substances. When storing, a suitable container should be selected to ensure a good seal. During transportation, the packaging should be properly protected to avoid package damage due to bumps, collisions, etc.
Because of its certain chemical activity, storage and transportation should avoid contact with strong oxidants, strong acids, strong bases and other substances to prevent violent chemical reactions and endanger safety. Only by paying careful attention to the above points during storage and transportation can the quality and stability of 4-iodo-1-tritylimidazole be ensured.