3-hydroxy-4-iodobenzonitrile

3-Hydroxy-4-iodobenzonitrile is one of the organic compounds. It has unique chemical properties, let me tell you one by one.
In this compound, the hydroxyl group (-OH), the iodine atom (-I) and the benzonitrile group (-CN) coexist on the benzene ring. The hydroxyl group has active properties and can participate in many chemical reactions. Because its oxygen atom has lone pairs of electrons, it can exhibit acidity and can neutralize with bases to form corresponding salts. And the hydroxyl group can participate in the esterification reaction, and under appropriate conditions, it can be dehydrated and condensed with organic acids to form ester compounds.
Iodine atoms in molecules have a certain polarity due to their large atomic radius and moderate electronegativity. They can participate in nucleophilic substitution reactions, and iodine atoms can be replaced by other nucleophilic reagents, which is an important way to construct new carbon-heteroatom bonds.
In benzonitrile groups, cyano (-CN) is a strong electron-absorbing group, which can reduce the electron cloud density of the benzene ring and affect the substitution reaction activity on the benzene ring. Cyano groups can undergo hydrolysis reactions, and under acidic or basic conditions, they can be gradually converted into carboxyl groups (-COOH) or amide groups (-CONH ²), etc., thereby deriving a series of different compounds.
In addition, 3-hydroxy-4-iodobenzonitrile has its physical properties due to the interaction of various groups in the molecule. Its solubility in organic solvents is affected by each group. The presence of hydroxyl groups makes it have a certain affinity for some polar organic solvents, and the benzene ring and cyanide groups affect its dispersion in non-polar solvents.
In short, the chemical properties of 3-hydroxy-4-iodobenzonitrile are rich and diverse, and the interaction of various groups provides a broad space for organic synthesis and chemical research.

There are various ways to synthesize 3-hydroxy-4-iodobenzonitrile. First, 3-hydroxy benzonitrile can be used as the starting material. First, a suitable iodine substitution reagent, such as iodine elemental substance (I ³), is matched with an appropriate oxidant, and under suitable reaction conditions, the iodine substitution reaction occurs at a specific position on the benzene ring. In this process, the reaction temperature, reaction time and reagent dosage need to be precisely regulated. If the temperature is too high, it may cause an increase in side reactions; if the temperature is too low, the reaction rate will be delayed. Time control is also critical. If it is too short, the reaction will be incomplete, and if it is too long, it may cause an overreaction. The proportion of reagents is out of balance, and it is difficult to achieve the ideal yield.
Second, we can start from 4-iodobenzoic acid. First, the carboxyl group is converted into an amide. The commonly used method is to use an appropriate amine reagent under the action of a condensing agent such as dicyclohexyl carbodiimide (DCC) to achieve the conversion. Then, the amide is dehydrated under the action of a dehydrating agent to form a nitrile group to obtain 3-hydroxy-4-iodobenzonitrile. In this route, the choice of reaction conditions at each step is also the key to success or failure. The condensation reaction requires consideration of factors such as solvent polarity and catalyst type, and the dehydration reaction requires strict requirements on the activity of the dehydrating agent and the reaction environment.
Third, using suitable halogenated aromatics as raw materials, cyanyl groups are introduced through metal-catalyzed cyanylation, and then the target product is expected to be synthesized through the hydroxylation step. In this process, the choice of metal catalysts is extremely important, and the activity and selectivity of different metal catalysts vary, which affects the direction and yield of the reaction. The hydroxylation step also requires the selection of appropriate hydroxylation reagents and reaction conditions to efficiently synthesize 3-hydroxy-4-iodobenzonitrile.

3-Hydroxy-4-iodobenzonitrile is one of the organic compounds. It has a wide range of uses and is of great significance in many fields.
Bearing the brunt, it can be used as a key intermediate in the field of medicinal chemistry. In the process of pharmaceutical research and development, the synthesis of many drugs relies on this as a starting material. Due to its structural characteristics, it can introduce different functional groups through chemical modification and reaction, and then construct compounds with diverse structures to meet the needs of different pharmacological activities. Or through a specific reaction path, it can be coupled with other compounds to create new drugs with unique curative effects to fight various diseases.
Furthermore, in the field of materials science, 3-hydroxy-4-iodobenzonitrile is also available. In the preparation of organic optoelectronic materials, its unique chemical structure can be used to adjust the electronic properties and optical properties of the materials. After rational molecular design and assembly, key performance indicators such as conductivity and luminous efficiency of materials may be improved, providing assistance for the development of new optoelectronic devices, such as organic Light Emitting Diodes, solar cells, etc.
Again, in the fine chemical industry, as a fine chemical, it is often used to prepare special properties of dyes, pigments, etc. Due to the characteristics given by its own structure, the resulting dyes and pigments can have unique colors, stability, and affinity for specific substrates, meeting the needs of high-quality colorants in industries such as textile printing and dyeing, ink manufacturing, etc.
In summary, 3-hydroxy-4-iodobenzonitrile is an indispensable raw material in many fields such as medicine, materials, and fine chemicals, and is of great significance for promoting technological progress and product innovation in various fields.

I think what you are asking is about the market price of 3-hydroxy-4-iodobenzonitrile. However, the price of this chemical is difficult to set abruptly. The price of this chemical is often changed due to many factors, such as the trend of supply and demand, the price of raw materials, production techniques, trade conditions, and even regional differences and seasonal changes.
If it comes to supply and demand, if the market demand for this product is very high and the supply is limited, the price will be higher; conversely, if the supply exceeds the demand, the price will drop. The price of raw materials is also the key. If the raw materials required for its preparation are expensive, the price of the finished product will not be cheap. The coarseness of production technology is also related to cost. Advanced techniques may reduce consumption and improve efficiency, making prices more competitive.
Furthermore, the trade environment also has an impact. The increase or decrease of tariffs and the existence of trade barriers can make prices fluctuate. Prices vary from region to region. In distant places, transportation costs are imposed on them, and prices may be higher. Seasonal changes can also cause prices to fluctuate for certain chemicals that depend on raw materials or production requirements in a specific season.
To know the exact market price, you should carefully study chemical market information, consult chemical suppliers, traders, or refer to professional chemical price reports to obtain relatively accurate numbers. It is impossible to rely on speculation.

For 3-hydroxy-4-iodobenzonitrile, many matters should be paid attention to during storage and transportation. This is an organic compound, and its properties may change due to the environment. Therefore, when storing, the temperature and humidity of the environment should be the first priority. It should be stored in a cool and dry place to avoid high temperature and humidity. High temperature can easily cause it to decompose, and moisture may cause chemical reactions that damage its quality.
In addition, it may be toxic and irritating. When storing, it must be isolated from food, beverages and other incompatible substances to prevent contamination and accidental ingestion. And it should be kept out of the reach of children to ensure the safety of personnel.
During transportation, caution should also be taken. The packaging must be tight, and suitable packaging materials should be selected to prevent leakage. The loading and unloading process must be handled with care to avoid violent vibration and collision, so as to avoid package damage.
In addition, the means of transportation should also be clean and dry, and there should be no residues that may react with it. At the same time, the transportation personnel should be familiar with its characteristics and emergency treatment methods. In case of accidents such as leakage, they can respond quickly and minimize the harm. In this way, 3-hydroxy-4-iodobenzonitrile is safe and secure during storage and transportation, and the quality is not damaged.