2 Bromo 7 Iodo 9h Fluoren
Iodobenzene

2 Bromo 7 Iodo 9h Fluoren

Fengxi Chemical

Specifications

HS Code

947875

Name 2-bromo-7-iodo-9H-fluorene
Molecular Formula C13H8BrI
Molecular Weight 385.91
Appearance Solid (predicted)
Chemical Formula C13H8BrI
Molecular Weight 371.91
Appearance Solid (predicted)
Solubility In Water Insoluble (predicted)
Solubility In Organic Solvents Soluble in common organic solvents (predicted)
Stability Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula C13H8BrI
Molecular Weight 371.91
Appearance Solid (predicted)
Solubility In Water Insoluble (predicted)
Chemical Formula C13H7BrI
Molecular Weight 379.905
Appearance Solid (predicted)
Boiling Point 423.7°C at 760 mmHg (predicted)
Melting Point 198 - 200°C
Density 2.035 g/cm³ (predicted)
Flash Point 210.1°C (predicted)
Solubility Insoluble in water (predicted)
Logp 5.62 (predicted)
H Bond Acceptors 0
H Bond Donors 0
Packing & Storage
Packing 100g of 2 - bromo - 7 - iodo - 9H - fluorene in a sealed, labeled chemical - grade bottle.
Storage **Storage for 2 - bromo - 7 - iodo - 9H - fluorene**: Store this chemical in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly sealed container to prevent moisture and air exposure, which could potentially lead to decomposition. It should be separated from oxidizing agents and incompatible substances.
Shipping 2 - bromo - 7 - iodo - 9H - fluorene should be shipped in well - sealed, corrosion - resistant containers. Ensure compliance with chemical transport regulations, with proper labeling indicating its nature and handling precautions during transit.
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2-bromo-7-iodo-9h-fluoren 2-bromo-7-iodo-9h-fluoren 2-bromo-7-iodo-9h-fluoren
General Information
Frequently Asked Questions
What is the chemistry of 2-bromo-7-iodo-9h-fluoren?
2-Bromo-7-iodine-9H-fluorene, this is an organic compound with unique chemical properties. Its chemical activity is high, or it shows special reactivity due to the presence of bromine and iodine atoms.
Let's talk about bromine and iodine atoms first. They have strong electronegativity and cause uneven distribution of molecular electron clouds, making this compound an ideal target for electrophilic reagents. It can undergo nucleophilic substitution reactions, and halogen atoms are replaced by nucleophiles. In case of hydroxyl or amino nucleophiles, bromine or iodine atoms may be replaced to give birth to new organic compounds, which are of great significance in the field of organic synthesis and can be used to construct diverse organic molecular structures.
In addition to the conjugated system, the 9H-fluorene matrix has a conjugated structure, which endows the molecule with certain stability and special photoelectric properties. Electrons in the conjugated system are delocalized, so that the compound may have certain fluorescence properties. In the field of materials science, it may be used to prepare fluorescent materials for devices such as organic Light Emitting Diodes.
In addition, the solubility of the compound may be special because its structure contains hydrophobic fluorene groups and halogen atoms. The solubility in organic solvents may be better than that of water. This property needs to be taken into account in its synthesis, separation and application. The solvent is selected for the synthesis reaction to ensure that the compound is well dissolved and the reaction proceeds smoothly.
Its chemical properties are also affected by surrounding substituents and reaction conditions. Different reaction conditions such as temperature, catalyst, etc., or the reaction path and product differences. When the temperature increases, the reaction rate may be accelerated, and the reaction selectivity may change. Appropriate catalysts can reduce the activation energy of the reaction and change the direction and efficiency of the chemical reaction.
What are the physical properties of 2-bromo-7-iodo-9h-fluoren?
2-Bromo-7-iodine-9H-fluorene is one of the organic compounds. Its physical properties are quite unique, and it is important to explore the properties, melting point, and solubility of this substance.
First of all, under normal temperature, 2-bromo-7-iodine-9H-fluorene is often in a solid state, and its appearance may be white to light yellow crystalline powder with fine texture. This appearance can be seen in many organic synthesis reactions.
As for the melting boiling point, the melting point of 2-bromo-7-iodine-9H-fluorene is quite high, about [X] ° C. Such a high melting point is due to the interaction forces between molecules, such as van der Waals forces, hydrogen bonds, etc. The presence of bromine and iodine atoms in the molecular structure enhances the intermolecular forces. To make it from a solid state to a liquid state, it needs to supply more energy, so the melting point is very high. The boiling point is also related to it, and its boiling point is about [X] ° C. A higher boiling point also indicates that the stability of the compound is relatively strong.
In terms of solubility, 2-bromo-7-iodine-9H-fluorene exhibits a certain solubility in organic solvents, such as dichloromethane, chloroform, toluene, etc. Because the molecular structure of the compound has a certain hydrophobicity, which is in line with the intermolecular force of the organic solvent, it is soluble. However, in water, its solubility is very small, because water is a polar solvent, while 2-bromo-7-iodine-9H-fluorene molecules have weak polarity, and the interaction between the two forces is difficult to defeat the hydrogen bond between water molecules, so it is difficult to dissolve in water.
In addition, the density of 2-bromo-7-iodine-9H-fluorene is also one of its physical properties. Its density is about [X] g/cm ³, which is different from that of common organic solvents. This property is of great significance in separation, purification and other operations.
Looking at its physical properties, it can be seen that 2-bromo-7-iodine-9H-fluorene is used in organic synthesis, materials science and other fields, and has specific uses due to these properties. For example, due to its high melting point, it can be used to prepare materials that require high temperature resistance; its solubility in organic solvents facilitates chemical reactions in solution systems, providing convenience for the synthesis of more complex organic compounds.
What are the common synthetic methods of 2-bromo-7-iodo-9h-fluoren?
The common synthesis method of 2-bromo-7-iodine-9H-fluorene is a key research in the field of organic synthesis. This synthesis often follows a multi-step reaction path to reach the target product.
The first step is to prepare a suitable fluorene derivative substrate. The acquisition of fluorene matrix, or separation from coal tar, or synthesis through a specific organic reaction.
Second, for the bromination step, brominating reagents can be selected, such as liquid bromine (Br 2) and suitable catalysts, such as iron powder (Fe) or iron tribromide (FeBr
). Under this catalysis, liquid bromine reacts with fluorene derivatives in specific solvents, such as dichloromethane (CH 2O Cl ³), and bromine atoms are selectively added to specific positions in the fluorene ring according to positioning rules to form bromine-containing fluorene intermediates.
Furthermore, the iodization process is also key. Commonly used iodizing reagents such as potassium iodide (KI) and appropriate oxidants such as hydrogen peroxide (H 2O ³) or potassium persulfate (K 2O S 2O). Under suitable reaction conditions, the iodizing reagent provides an iodine source, and the oxidant promotes the oxidation of iodine ions into active iodine species, and then reacts with bromine-containing fluorene intermediates to introduce iodine atoms into the target site, resulting in 2-bromo-7-iodine-9H-fluorene products.
During the reaction, many factors need to be finely regulated. The temperature significantly affects the reaction rate and selectivity. Too low temperature, the reaction is slow and the yield is low; too high temperature, or cause frequent side reactions, and the purity of the product is damaged. The choice of solvent is also crucial. Its properties such as polarity and solubility are related to the dispersion, reactivity and product separation of the reactants.
In addition, the reaction time also needs to be precisely controlled. If it is too short, the reaction will not be completed, and if it is too long, the product will decompose or overreact. In order to improve the purity and yield of the product, the post-reaction treatment steps are indispensable, often involving extraction, washing, drying, column chromatography or recrystallization to separate and purify the target product.
2-bromo-7-iodo-9h-fluoren in what areas
2-Bromo-7-iodine-9H-fluorene is useful in various fields. In the field of materials science, it is highly valued in the preparation of organic optoelectronic materials due to its unique chemical structure. The manufacture of organic Light Emitting Diode (OLED), which can be used as a key luminescent material, can effectively adjust the luminescent color and efficiency, making the OLED display more colorful and lower energy consumption.
In the field of medicinal chemistry, 2-bromo-7-iodine-9H-fluorene may have potential biological activity. Researchers use it as a starting material and chemically modify it in a series to obtain new compounds with specific pharmacological effects. Or it can act on specific biological targets, paving the way for the development of new drugs, such as anti-cancer and anti-inflammatory drugs.
Furthermore, it is also useful in the field of material surface modification. It can be grafted on the surface of the material by chemical reaction to change the surface properties of the material, such as wettability and adhesion. In this way, in the coating, fabric treatment and other industries, the product performance can be better, such as better adhesion of coatings and better waterproof and anti-fouling performance of fabrics.
In organic synthesis chemistry, 2-bromo-7-iodine-9H-fluorene is often used as an important intermediate. Because it contains active functional groups such as bromine and iodine, it is convenient to undergo nucleophilic substitution, coupling and other reactions with other organic reagents, which helps researchers construct complex organic molecules and provides assistance for the synthesis of new functional materials and the total synthesis of natural products.
What is the market outlook for 2-bromo-7-iodo-9h-fluoren?
Today, I have a question about the market prospects of 2-bromo-7-iodine-9H-fluorene. This is an organic compound with potential applications in chemical and material fields.
First, the chemical field. In organic synthesis, it can be used as a key intermediate. Due to the special chemical activity of bromine and iodine, it can introduce other functional groups through many chemical reactions to build complex organic molecules. The pharmaceutical industry often relies on such intermediates to create new drugs, such as the development of antibacterial and anticancer drugs. With the advance of medical technology, the demand for novel and efficient drugs is increasing, and 2-bromo-7-iodine-9H-fluorene as a potential intermediate may welcome more opportunities.
Times and materials fields. In the field of optoelectronic materials, fluorene compounds are famous for their unique optical and electrical properties. 2-bromo-7-iodine-9H-fluorene can be modified and polymerized, or materials with special optoelectronic properties can be prepared for use in organic Light Emitting Diodes (OLED), solar cells, etc. The OLED display market has expanded rapidly in recent years, and the demand for related optoelectronic materials has increased sharply. This compound may find room for development in the meantime.
However, its market prospects are also constrained by several factors. The first is the cost of synthesis. If the synthesis process is complicated and the raw materials are expensive, the price of the product will be high and its large-scale application will be restricted. Furthermore, environmental protection requirements are becoming stricter and stricter. If a large number of pollutants are generated in the synthesis process, it will not conform to the concept of green chemistry and will be rejected by the market.
Overall, 2-bromo-7-iodine-9H-fluorene has a considerable market prospect. However, in order to fully explore, researchers need to optimize the synthesis process, reduce costs and increase efficiency, and be green and environmentally friendly. The industry also needs to have a keen insight into market demand, and urge it to move from the laboratory to the market, so as to contribute to the development of chemical