3 Iodo 7 Azaindole
Iodobenzene

3 Iodo 7 Azaindole

Fengxi Chemical

Specifications

HS Code

453273

Chemical Formula C7H5IN2
Molecular Weight 246.03 g/mol
Appearance Solid (predicted from similar compounds)
Melting Point No data (common for less - studied heterocyclic iodides, would need experimental determination)
Boiling Point No data (estimation difficult without experimental data, likely high due to polar and aromatic nature)
Solubility In Water Low (due to non - polar aromatic and hydrophobic iodo group)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (due to aromatic and non - ionic nature)
Pka No data (for the 7 - azaindole moiety, pKa of related azaindoles can be in the range of 1 - 3 for the conjugate acid, but specific for this iodo - derivative needs determination)
Stability Stable under normal conditions, but may be sensitive to light and strong oxidizing agents (iodine - containing compounds can be photo - sensitive)
Color Colorless to pale yellow (predicted from related iodinated heterocyclic compounds)
Chemical Formula C7H5IN2
Molecular Weight 246.03 g/mol
Appearance Solid
Color Off - white to light yellow
Melting Point 180 - 184 °C
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in common organic solvents like DMSO, DMF
Stability Stable under normal conditions, but may be light - sensitive
Chemical Formula C7H5IN2
Molecular Weight 246.03
Appearance Solid
Color Typically off - white to light yellow
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in common organic solvents like DMSO, DMF
Melting Point 180 - 184 °C
Pka Relevant pKa values related to its acidic or basic groups can be in a certain range depending on the environment
Density Data may vary, but typically in the range of organic solid densities
Stability Stable under normal conditions, but sensitive to light and air over time
Packing & Storage
Packing 100g of 3 - iodo - 7 - azaindole packaged in a sealed, labeled chemical - grade bottle.
Storage 3 - iodo - 7 - azaindole should be stored in a cool, dry place, away from direct sunlight. It is advisable to keep it in a tightly sealed container to prevent exposure to air and moisture, which could potentially lead to degradation. Store it in a location separate from incompatible substances, such as strong oxidizing agents, to ensure safety and maintain its chemical integrity.
Shipping 3 - iodo - 7 - azaindole, a chemical, will be carefully packaged to prevent breakage. Shipped via a reliable carrier, ensuring proper handling and compliance with chemical transport regulations for safe and timely delivery.
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3-iodo-7-azaindole 3-iodo-7-azaindole 3-iodo-7-azaindole
General Information
Frequently Asked Questions
What is the main use of 3-iodo-7-azaindole?
3-Iodo-7-azaindole, Chinese name 3-iodo-7-azaindole, is an important organic compound, which is widely used in the fields of medicinal chemistry and materials science.
In the field of medicinal chemistry, this compound is mainly used in drug development. Due to its unique chemical structure, it can be used as a key intermediate to participate in the synthesis of many biologically active compounds. Taking the development of anti-cancer drugs as an example, scientists have found that drug molecules containing 3-iodo-7-azaindole structure have significant inhibitory effects on specific cancer cells. The iodine atom and azaindole ring in its structure can precisely act on specific biological targets in cancer cells, or affect the signaling pathways related to cancer cell proliferation, or hinder the activities of key enzymes in cancer cell metabolism, thereby inhibiting the growth and spread of cancer cells. In the development of antiviral drugs, studies have also shown that compounds based on this have inhibitory effects on certain viruses, and play an antiviral effect by interfering with the binding process of viruses to host cells, or inhibiting the replication of viruses in host cells.
In the field of materials science, 3-iodo-7-azaindole can be used to prepare functional materials. For example, in organic optoelectronic materials, its special electronic structure makes the material exhibit unique optoelectronic properties. Introducing it into the organic Light Emitting Diode (OLED) material system can optimize the luminous efficiency and stability of the material. Because the 3-iodo-7-azaindole structure can regulate the charge transfer and energy transfer process between the molecules of the material, the OLED device can emit light more efficiently under electric excitation and prolong the service life of the device. In terms of sensor materials, high sensitivity and high selectivity sensors can be constructed based on their specific interactions with specific substances. For example, for some metal ions or biomolecules, 3-iodo-7-azaindole can undergo detectable physical or chemical changes with them, so as to achieve sensitive detection of target substances.
What are the physical properties of 3-iodo-7-azaindole?
3-Iodo-7-azaindole is an organic compound with unique physical properties. Its properties are usually solid, and the intermolecular forces are unique due to the iodine atom and 7-azaindole core structure in the molecular structure. The melting point is closely related to the molecular accumulation and interaction. However, the specific melting point data needs to be accurately determined by experiments, because different preparation methods and purity can affect the melting point.
The solubility of this substance is also an important physical property. In organic solvents, its solubility depends on the force between the solvent and the solute. Generally speaking, because of its certain polarity, it should have good solubility in polar organic solvents such as dimethyl sulfoxide (DMSO) and N, N-dimethylformamide (DMF), because these solvents can form hydrogen bonds or dipole-dipole interactions with 3-iodo-7-azaindole. In non-polar organic solvents such as n-hexane, the solubility is not good, because the non-polar solvent and the polar 3-iodo-7-azaindole have a certain polarity.
In addition, the density of 3-iodo-7-azaindole is also one of its physical properties. Density is closely related to molecular mass and molecular accumulation, but the exact density value also needs to be accurately determined experimentally. The relative atomic mass of iodine atoms in molecules is relatively large, which contributes a lot to the overall molecular mass, which may affect the density.
Its appearance may vary depending on purity and crystallization conditions. High purity 3-iodo-7-azaindole or white to light yellow crystalline powder, if it contains impurities, the appearance color and morphology may change.
In summary, the physical properties of 3-iodo-7-azaindole, such as melting point, solubility, density, appearance, etc., are crucial for its application in organic synthesis, drug development and other fields. However, the exact values of many properties often require accurate experimental determination and are subject to various factors.
What are the synthesis methods of 3-iodo-7-azaindole?
3-Iodo-7-azaindole can be synthesized by various methods. The way of synthesis can be introduced into the iodine atom by halogenation through 7-azaindole as the starting material. In this method, a suitable halogenating reagent, such as iodine elemental substance, is selected with a suitable oxidizing agent, or a specific reagent containing iodine, such as N-iodosuccinimide (NIS), is selected under suitable reaction conditions, so that the iodine atom can be successfully connected to the third position of 7-azaindole.
Furthermore, it can be obtained by multiple steps from other related compounds. For example, the skeleton of 7-azaindole is constructed from a pyridine derivative with appropriate substituents through a series of reactions such as cyclization and halogenation, and iodine atoms are introduced at the third position in a specific step. In this process, the cyclization reaction needs to find suitable conditions and reagents to form a ring structure of 7-azaindole, and then the substitution position of the iodine atom is precisely controlled during halogenation.
Or there is a method of transition metal catalysis. Using a specific metal catalyst, such as a palladium catalyst, with a suitable ligand, in a reaction system common in organic synthesis, the iodine-containing reagent is coupled to the 7-azaindole precursor, thereby introducing the iodine atom into the target position. This method of transition metal catalysis often requires fine regulation of the reaction substrate, catalyst, ligand and reaction conditions to obtain good reaction yield and selectivity.
There are many methods for the synthesis of 3-iodo-7-azaindole, and each method has its own advantages and disadvantages. In practical application, it is necessary to choose the appropriate one according to specific circumstances, such as the availability of raw materials, the difficulty of reaction, and the consideration of cost.
What fields is 3-iodo-7-azaindole used in?
3-Iodo-7-azaindole is an organic compound that has outstanding uses in many fields such as medicinal chemistry and materials science.
In the field of medicinal chemistry, it is widely involved in the development of innovative drugs as a key intermediate. Due to its unique chemical structure, it can closely bind to specific biological targets and demonstrate potential biological activity. For example, it may be used to develop anti-tumor drugs, which can inhibit the proliferation and spread of cancer cells by precisely regulating specific molecular pathways of cancer cells, bringing new hope for solving cancer problems; in the research and development of drugs for neurological diseases, it may also use its structural properties to regulate neurotransmitter transmission or nerve cell activity, providing new ideas for the treatment of neurological diseases such as Alzheimer's disease and Parkinson's disease.
In the field of materials science, 3-iodo-7-azaindole can be used as the cornerstone of functional materials. Because of its iodine atom and azaindole structure, the material is endowed with unique electrical and optical properties. In the field of organic photovoltaic materials, it may be used to prepare high-efficiency organic Light Emitting Diodes (OLEDs), improve luminous efficiency and stability, and promote display technology to a higher level; in the research and development of organic solar cell materials, with its structural advantages, enhance the absorption of light and charge transport capacity, improve the photoelectric conversion efficiency of solar cells, and open up new ways for renewable energy utilization.
To sum up, 3-iodo-7-azaindole has great potential in the fields of medicine and materials science. With in-depth research, it will surely bloom in more fields and contribute an important force to the progress of human society.
What is the market outlook for 3-iodo-7-azaindole?
3-Iodo-7-azaindole is one of the organic compounds. Looking at its market prospects today, it is quite promising.
From the perspective of pharmaceutical research and development, such compounds may play a key role in the process of innovative drug creation. Because of its unique structure, it has potential biological activity, or can show pharmacological effects on specific disease targets. For example, in the development of anti-cancer drugs, researchers are exploring the mechanism of its interaction with cancer cells, hoping to develop new anti-cancer drugs with excellent efficacy and low side effects by modifying and optimizing its structure.
In the field of materials science, 3-iodo-7-azaindole also has application opportunities. It may be the cornerstone of new organic materials, endowing materials with specific properties such as photoelectric properties and thermal stability. For example, in the research and development of organic Light Emitting Diode (OLED) materials, rational design and synthesis may improve the luminous efficiency and service life of OLED devices, thereby promoting the innovation of display technology.
Furthermore, with the progress of science and technology and the deepening of research, related synthesis technologies are also constantly improving. More efficient and green synthesis paths are gradually emerging, which can not only reduce production costs, but also conform to environmental protection concepts, lay a solid foundation for large-scale production, and further expand the breadth and depth of its market applications.
However, its market development is not smooth sailing, but also faces challenges. On the one hand, strict regulations and safety assessments set a threshold for its entry into the market; on the other hand, the highly competitive market environment requires developers to continuously introduce new products and improve product quality and performance in order to occupy a place in the market. Overall, although 3-iodo-7-azaindole faces challenges, the market prospect is still broad due to its unique properties and potential applications, which is worthy of all parties' investment in exploration and development.