2-Pyridinecarbonitrile,5-hydroxy-3-methyl-(9CI)

2-Pyridinecarbonitrile, 5-hydroxy-3-methyl (9CI), this is an organic compound. Its physical properties, at room temperature or as a solid, but the specific melting point, boiling point, etc., need to be accurately determined by experiments. Looking at its structure, the pyridine ring is aromatic, resulting in a certain stability of the compound.
In terms of chemical activity, the nitrile group (-CN) is active and can participate in various reactions. If it can be hydrolyzed to carboxyl (-COOH) under specific conditions, this reaction is often catalyzed by acid or base, and the process is complicated, requiring fine regulation of the reaction conditions. Hydroxy (-OH) also affects the properties of the compound, and can participate in the esterification reaction and react with acids to form ester compounds. Although methyl (-CH
) is relatively stable, it affects the molecular space structure and electron cloud distribution, and indirectly affects the reactivity.
In terms of solubility, due to the presence of polar groups hydroxyl and nitrile groups, there may be a certain solubility in polar solvents (such as water and alcohols), but due to the presence of pyridine rings and methyl groups, their solubility in water is limited, and the solubility in organic solvents (such as dichloromethane, chloroform) may be better.
In chemical reactions, the compound can exhibit various reaction paths due to different reaction conditions and reagents. For example, under reduction conditions, the nitrile group may be reduced to an amino group (-NH ²) to derive amino-containing pyridine compounds. This process requires suitable reducing agents and reaction environments. In conclusion, 2-pyridylmethonitrile, 5-hydroxy-3-methyl (9CI) is rich in chemical properties and has potential application value in the field of organic synthesis.

The common synthesis methods of 2-pyridinecarbonitrile, 5-hydroxy-3-methyl (9CI) are as follows:
To obtain this compound, it is often the way of chemical synthesis. One method can be started from the raw material containing the pyridine ring. First take the appropriate pyridine derivative and introduce the cyanyl group at a specific position. This step can be achieved by nucleophilic substitution. Take the pyridine with the suitable substituent as the substrate and react with the cyanide reagent, such as potassium cyanide, sodium cyanide, etc., under a phase transfer catalyst or suitable solvent and conditions, so that the cyanyl group is connected to the pyridine ring.
Then, the hydroxyl group is introduced. Oxidation reaction can be used. If there are oxidizable groups on the pyridine ring, the hydroxyl group will be formed at the desired 5-position after being treated with suitable oxidizing agents, such as mild peroxides.
As for the addition of methyl groups, suitable methylating reagents can be selected, such as iodomethane, dimethyl sulfate, etc. Under basic conditions, react with pyridine derivatives to make methyl groups attached to the 3-position. During the reaction process, it is necessary to pay attention to the fine regulation of reaction conditions, such as temperature, pH, reaction time, etc., which have a great impact on the yield and purity of the reaction product. The choice of solvent is also critical. Different solvents may promote or inhibit the reaction, so careful consideration must be made. Thus, the compound 2-pyrimethanonitrile, 5-hydroxy-3-methyl (9CI) can be obtained by clever design and execution of multi-step reaction.

2-Pyridinecarbonitrile, 5-hydroxy-3-methyl (9CI) This substance has a wide range of uses and is involved in various fields.
In the field of medicine, it may be the key raw material for the creation of new drugs. Due to the unique chemical structure of this compound, it is endowed with specific biological activities and can interact with specific targets in the human body. It may be possible to develop specific drugs for diseases such as inflammation and tumors by modifying and modifying its structure, providing a new path for medical treatment to overcome difficult and complicated diseases.
In the field of materials science, it also has its uses. Due to its special chemical properties, it may participate in the synthesis of materials with unique properties. For example, it is expected to produce sensing materials with high sensitivity and selectivity to specific substances, which can be used to accurately detect specific pollutants in the field of environmental monitoring; or to synthesize optical materials with excellent performance, which can be used in optical displays, optoelectronic devices, etc., to improve the performance of related products.
In the field of organic synthesis, this compound is an important cornerstone. With its activity check point, it can be reacted through various organic reactions to build more complex organic molecular structures. Organic chemists often use this as a starting material to synthesize a series of organic compounds with novel structures and unique functions through exquisite design of reaction routes, which contribute to the development of organic synthetic chemistry and promote the field to continuously expand the boundaries and explore more unknown possibilities.

Today, there are 2-pyridinonitrile, 5-hydroxy-3-methyl (9CI). What is the market prospect? Let me tell you in detail.
Looking at the chemical market in the world, there are many changes, such as the unpredictable situation. 2-pyridinitrile, 5-hydroxy-3-methyl (9CI) such substances may have their unique uses in various fields of chemical industry. However, its market prospects must be viewed from several angles.
The first one is related to its use. If this substance is used in medicine, pesticides, materials and other industries, it is an indispensable raw material, can help various industries to improve, and the effect is significant, then its demand may be prosperous. The industry of medicine is related to the health of people's livelihood. If it can be used as medicine to cure diseases, it must be valued by doctors, and the market is also broad. The genus of pesticides is related to harvesting, which can protect crops from diseases and pests, and farmers must also ask for it. Its market should not be underestimated.
Furthermore, it depends on its production capacity. If there are many producers, and the supply exceeds the demand, the price will fall, and the market situation will be worrying. However, if there are few producers, and there are many applicants, and the supply exceeds the demand, its price will rise, and the future will be bright. And if the technology of the product can be refined, the cost can be reduced and the quality can be increased, it can also increase the competitiveness of the market.
And look at the dynamics of the market. The world's technology is new, and new products are emerging one after another. If there are other products that can replace 2-pyridyl formonitrile and 5-hydroxy-3-methyl (9CI), and it is better, then its market will be impacted. On the contrary, if it has no replacement and dominates, its market will thrive.
In summary, the market prospects of 2-pyridyl formonitrile and 5-hydroxy-3-methyl (9CI) are not one word. It is necessary to observe its use, production capacity and market changes, and weigh the various ends before we can know its approximation. Those who are widely used, suitable for production, and irreplaceable will have a bright future; if they do the opposite, they may encounter difficulties. However, the market is changing rapidly, and it is necessary to pay attention at any time and evaluate the situation in order to seize the opportunity.

2-Pyridineformonitrile, 5-hydroxy-3-methyl- (9CI), this compound is an organic compound, often used as a key intermediate in the field of chemical synthesis. The following upstream and downstream products:
Upstream products: The selection of raw materials is very important. Pyridine compounds can be used as starting materials. For example, a specific substituted pyridine is halogenated to introduce a halogen atom, which then undergoes a nucleophilic substitution reaction with a cyanide reagent, and a cyanide group is introduced into the pyridine ring. The hydroxyl group in the molecule of 5-hydroxy-3-methylpyridineformonitrile can be constructed by the nucleophilic substitution reaction of phenolic compounds or the hydroxyl-aldehyde condensation of aldehyde-ketone compounds. The introduction of methyl groups can be carried out with the help of methylating reagents, such as iodomethane, under appropriate basic conditions, nucleophilic substitution reactions occur with specific positions on the pyridine ring.
Downstream products: Based on this substance, cyano groups can be converted into amino groups through reduction reactions to obtain corresponding pyridine methylamine derivatives. Such derivatives are often used in the field of medicinal chemistry to construct molecular structures with biological activity. The reactivity of hydroxyl groups can also be used to esterify with acid chlorides or acid anhydrides to form ester compounds, which are widely used in the fields of fragrances, plasticizers, etc. If they are allowed to condensate with compounds containing active hydrogen under alkali catalysis, more complex heterocyclic systems can be constructed, which has potential application value in the fields of new materials and pesticides.