1h Indazole 6 Iodo
Iodobenzene

1h Indazole 6 Iodo

Fengxi Chemical

Specifications

HS Code

685581

Chemical Formula C7H5IN2
Molecular Weight 260.03 g/mol
Appearance Solid (likely white or off - white powder)
Physical State At Room Temperature Solid
Melting Point Data may vary, needs experimental determination
Boiling Point Data may vary, needs experimental determination
Solubility In Water Low solubility, likely sparingly soluble
Solubility In Organic Solvents May be soluble in common organic solvents like dichloromethane, chloroform
Pka No common reported value, needs experimental determination
Density Data may vary, needs experimental determination
Chemical Formula C7H5IN2
Molecular Weight 260.03 g/mol
Appearance Solid (likely a colored powder or crystal)
Solubility In Water Poor (due to its non - polar aromatic structure)
Solubility In Organic Solvents Likely soluble in common organic solvents like dichloromethane, chloroform, etc.
Uv Vis Absorption Absorption peaks can be found in the ultraviolet - visible spectrum due to its conjugated system
Chemical Formula C7H5IN2
Molecular Weight 260.03 g/mol
Appearance Solid (predicted from structure)
Solubility In Water Low solubility (aromatic and halogen - containing heterocycle)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (due to its organic nature)
Stability Stable under normal conditions, but may be sensitive to light and air (iodine - containing compound)
Chemical Formula C7H5IN2
Molecular Weight 260.03
Appearance Solid (usually white to off - white)
Melting Point Data may vary, typical organic solid melting range
Boiling Point Decomposes before boiling in normal conditions
Solubility In Water Poorly soluble
Solubility In Organic Solvents Soluble in some common organic solvents like DMSO, DMF
Density Data may be available in literature, likely in the range of common organic solids
Pka Relevant acid - base properties data may exist depending on indazole's functionality
Reactivity Reactive towards electrophiles due to presence of nitrogen and iodine
Packing & Storage
Packing 100g of 6 - iodo - 1H - indazole packaged in a sealed, chemical - resistant bottle.
Storage 1H - indazole, 6 - iodo - should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly sealed container to prevent moisture absorption and contact with air, which could potentially lead to decomposition or degradation. Store it separately from incompatible substances, like oxidizing agents and strong acids, to ensure safety.
Shipping 6 - iodo - 1H - indazole is a chemical. Shipping should follow strict regulations for hazardous or chemical substances. It must be properly packaged to prevent leakage, with clear labels indicating its nature for safe and compliant transportation.
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1h-indazole, 6-iodo- 1h-indazole, 6-iodo- 1h-indazole, 6-iodo-
General Information
Frequently Asked Questions
What are the main uses of 1H-indazole, 6-iodine?
1H-pyrrole, the main user of 6-chlorine, is involved in Tiangong Kaiji, and its use is quite wide.
1H-pyrrole, which is a nitrogen-containing five-membered heterocyclic compound, has unique chemical properties and is important in many fields. In the field of organic synthesis, 1H-pyrrole is often a key intermediate. Due to the characteristics of electron cloud distribution on the ring, various chemical reactions, such as electrophilic substitution, introduce different functional groups, and then synthesize many complex and special organic compounds.
6-chlorine, 1H-pyrrole can be modified to change its physical and chemical properties. In pharmaceutical chemistry, 1H-pyrrole derivatives modified with 6-chlorine may have specific biological activities. For example, some of these derivatives may act on specific biological targets in the human body, and have potential therapeutic effects on diseases, such as anti-cancer, antibacterial, etc. Doctors often make new drugs based on this to explore drugs with better efficacy and less side effects.
Furthermore, in the field of materials science, 1H-pyrrole and 6-chlorine related products are also used. Pyrrole can be polymerized to form conductive polymers, and the introduction of 6-chlorine may regulate its electrical conductivity and optical properties. These conductive polymers have important applications in electronic devices, such as organic Light Emitting Diodes (OLEDs), sensors and other fields. Workers make OLED screens, which can make the screens more efficient and colorful; sensors can make them more sensitive to specific substances.
In dye chemistry, 1H-pyrrole and 6-chlorine derivatives can be used as raw materials for dyes. Due to its unique light absorption and luminous properties, the dyes produced may have good dyeing properties and color fastness. Dyeing fabrics with this dye can make fabrics bright and long-lasting.
In conclusion, 1H-pyrrole and 6-chlorine are indispensable elements in many fields such as organic synthesis, medicine, materials, dyes, etc., promoting the development and progress of various industries.
What are the physical properties of 1H-indazole and 6-iodine?
1H-pyrrole, 6-bromine, is an organic compound. Its physical properties are quite unique, let me describe them in detail for you.
Looking at its properties, under room temperature, 1H-pyrrole, 6-bromine is often colorless to light yellow liquid, with a clear appearance and a special appearance. Its odor has a relatively strong and unique smell, which can be impressive. This smell can be an important characteristic in the identification of organic compounds.
On the boiling point, the boiling point of 1H-pyrrole, 6-bromine is in a specific temperature range. The value of its boiling point is roughly within a certain range due to different or slightly different conditions for accurate determination. The boiling point characteristic determines the temperature node of the state transition during the heating process, and is extremely critical in chemical operations such as separation and purification.
In terms of melting points, 1H-pyrrole and 6-bromine also have their inherent values. Under specific pressure and other conditions, when this melting point is reached, the substance will transform from solid to liquid. The characteristics of this melting point are of great significance in the identification of substances and the treatment of solid substances.
Solubility is also one of its important physical properties. 1H-pyrrole and 6-bromine exhibit certain solubility in organic solvents. For example, in common organic solvents such as ethanol and ether, it can be dissolved in them, while the solubility in water is relatively limited. The difference in solubility plays a key role in practical application scenarios such as material extraction and reaction medium selection.
Above the density, 1H-pyrrole and 6-bromine have specific density values. Compared with water and other common liquids, their density may be large or small. This property is an indispensable consideration in chemical processes involving delamination and other operations.
This is the physical property of 1H-pyrrole and 6-bromine. All properties are interrelated and have important value in the research of organic chemistry and the practice of chemical production.
What are the chemical properties of 1H-indazole, 6-iodine-
1H-pyrrole and 6-chlorine are a class of organic compounds with unique chemical properties. Its chemical properties are quite complex and show key effects in many fields.
When it comes to stability, the pyrrole ring in this compound exhibits a certain aromaticity due to the presence of nitrogen atoms, but its aromaticity is slightly weaker than that of typical aromatic hydrocarbons such as benzene. The substitution of 6-chlorine affects the electron cloud distribution to some extent, which changes the stability. Chlorine atoms have an electron-absorbing effect, which will reduce the electron cloud density on the pyrrole ring, thereby affecting its chemical activity and stability.
In the electrophilic substitution reaction, the pyrrole ring is relatively high in electron cloud density due to the conjugation of the lone pair of electrons of the nitrogen atom, so the electrophilic substitution reaction activity is high, and the reaction check point mostly occurs at the alpha-position (that is, the carbon atom adjacent to the nitrogen atom). The introduction of 6-chlorine, although the electron absorption reduces the electron cloud density on the ring and the electrophilic substitution activity slightly decreases, such reactions can still occur. For example, in reactions with halogenating reagents, nitrifying reagents, etc., the localization effect of chlorine atoms will also affect the reaction check point, sometimes making the reaction more inclined to a specific position.
In terms of acidity and alkalinity, pyrrole is slightly acidic, because hydrogen atoms on nitrogen atoms can be slightly ionized. After 6-chlorine substitution, the binding force of nitrogen atoms to hydrogen atoms is slightly changed due to the electron-absorbing action of chlorine, and the acidity may be slightly adjusted. However, in general, its acidity is still weak, and it can react with strong bases.
In addition, 6-chloro-1H-pyrrole also has properties in redox reactions. Under appropriate conditions, pyrrole rings can be oxidized, and the presence of chlorine atoms may affect the oxidation reaction path and product. In the reduction reaction, pyrrole rings also have certain reactivity and can be reduced to different degrees of saturated products, and the reaction conditions and product structure are affected by chlorine atoms.
In summary, 6-chloro-1H-pyrrole has unique chemical properties, such as stability, electrophilic substitution, acidity and alkalinity, and redox, which are all special due to the interaction between pyrrole rings and chlorine atoms. It has important research and application value in the fields of organic synthesis and medicinal chemistry.
What are the synthesis methods of 1H-indazole and 6-iodine?
There are many methods for synthesizing 1H-indazole and 6-chlorine, and several common ones are briefly described below.
One is to use o-nitrotoluene as the starting material. First, the o-nitrotoluene is halogenated, and chlorine atoms are introduced at a specific position to obtain chlorine-containing o-nitrohalotoluene. Then, the nitro group is reduced to an amino group. The commonly used reducing agents include ferric acid system or catalytic hydrogenation. The obtained o-amino chlorotoluene is then cyclized with reagents such as formic acid or formamide. After a series of complex electron rearrangement and cyclization processes, the final formation of 1H-indazole and 6-chlorine is obtained. The raw material of this path is easy to obtain, but the steps are slightly complicated, and the reaction conditions of each step need to be carefully controlled.
Second, phenylhydrazine and chloro-maleic anhydride are used as raw materials. Phenylhydrazine and chloro-maleic anhydride are condensed first to form hydrazone intermediates. Subsequently, under appropriate acid-base conditions, the intermediate undergoes intramolecular cyclization to construct an indazole ring system, and then generates the target product 1H-indazole and 6-chloro. This method is relatively simple and the reaction conditions are relatively mild, but the raw material cost may be higher.
Third, 2-chlorobenzoic acid is used as the starting material. First, 2-chlorobenzoic acid is converted to acid chloride, and chlorination reagents such as dichlorosulfoxide are commonly used. The obtained acid chloride is then reacted with sodium azide and rearranged by Curtius to form an isocyanate intermediate. The isocyanate intermediate undergoes intramolecular cyclization under appropriate conditions to generate 1H-indazole and 6-chlorine. This path involves azide, and the operation needs to be cautious, so that the structure of the target molecule can be efficiently constructed.
Synthesis of 1H-indazole and 6-chlorine has advantages and disadvantages. In practical application, the appropriate synthesis method should be comprehensively weighed according to factors such as raw material availability, cost considerations, reaction conditions and product purity requirements.
1H-indazole, 6-iodine - what is the price range in the market?
Today, there are 1H-pyrrole and 6-chlorine in the market. What is the price? This is a question that the market often asks. However, the range of prices is difficult to say in a word, and the price varies due to various reasons.
Looking at the market conditions of the man, the amount of production, the wide and narrow use of it, are all related to the price. If the product is abundant and not used widely, the price will be low; if the product is thin, and the users are in large numbers, and the demand is too high, the price will be high.
And the difference in the region of the husband is also related to the price. In Dayi, Tongdu, the business is convergent, the logistics is convenient, and the price is flat; in remote places, it is difficult to transfer, and the price may increase.
Furthermore, as time goes by, the price also changes. Invesco is on duty, and the products are abundant, and the price stabilizes or decreases; in case of age apology, or changes in government orders, the price is unpredictable.
According to common sense, the prices of 1H-pyrrole and 6-chlorine range from tens to hundreds of dollars per gram. However, this is only an approximate number. To know the exact price, you can only get it when you visit Jia people in various cities and ask people who sell this product. And the city is unstable, and the price is variable, and the real-time situation must prevail.