1H-imidazo[4,5-b]pyridine-2-carboxylic acid, 5-chloro-

5-Chloro-1H-imidazolo [4,5-b] pyridine-2-carboxylic acid, this is an organic compound. It has unique chemical properties.
In terms of physical properties, this compound is mostly solid, but the specific color state varies according to its purity and crystallization, or it is white to off-white powder, or crystalline. The melting point is also a key physical property. The specific melting point value is helpful for identification and purity determination, but the exact melting point needs to be accurately determined by experiments.
Chemical properties, because its structure contains carboxyl groups, it is acidic and can neutralize with bases to form corresponding carboxylate. And carboxyl groups can participate in many reactions, such as esterification reactions, and react with alcohols under suitable conditions to form ester compounds.
Furthermore, the imidazolopyridine part in its structure is rich in nitrogen atoms, which endows the compound with certain basicity and coordination ability. Nitrogen atoms can provide lone pairs of electrons, form coordination bonds with metal ions, etc., to construct coordination compounds. This property has potential application value in the fields of materials science and biomedicine.
Because of its chlorine atoms, under suitable conditions, chlorine atoms can participate in substitution reactions, providing the possibility of introducing other functional groups, and then expanding the derivatization path of the compound, which can be used to construct more complex molecular structures in organic synthesis. The chemical properties of 5-chloro-1H-imidazolo [4,5-b] pyridine-2-carboxylic acids have attracted much attention in the fields of organic synthesis and medicinal chemistry, laying the foundation for many studies and applications.

5-Chloro-1H-imidazolo [4,5-b] pyridine-2-carboxylic acid, this substance has a wide range of uses. In the field of pharmaceutical development, it is often used as a key intermediate. It can be converted into compounds with specific pharmacological activities by specific chemical means through a series of reactions, and can be used to create drugs for the treatment of various diseases, such as inflammation, tumors and other related diseases.
In the field of materials science, it also has its unique applications. Its structural properties make it possible to participate in the construction of new functional materials, such as materials with special optical and electrical properties, opening up new paths for material research and development. In the field of chemical synthesis,

is often used as a reaction substrate. It is cleverly designed with various reagents to generate compounds with novel structures and research value and application potential, which helps to expand and deepen organic synthetic chemistry.
Because of its unique chemical structure and activity, it has become the focus of many researchers in scientific research and exploration, in order to deeply explore its reaction mechanism, performance characteristics, etc., and provide theoretical and practical support for innovative development in many fields.

There are currently methods for the synthesis of 5-chloro-1H-imidazolo [4,5-b] pyridine-2-carboxylic acids, which are described in detail as follows.
First take a suitable pyridine derivative and use it as the starting material. In the reaction vessel, add an appropriate amount of chlorination reagent. This chlorination reagent should be carefully selected according to the characteristics and requirements of the reaction, and control the reaction temperature, time and proportion of materials. After the chlorination reaction, the chlorine atom is introduced into the pyridine ring at a specific position to form a chlorine-containing pyridine intermediate.
Then, for this intermediate, the imidazole ring structure is introduced. Select a suitable imidazolylation reagent and make it react with the intermediate under suitable reaction conditions. This reaction condition covers the choice of reaction solvent, the regulation of pH and the precise control of temperature. Through a series of reaction steps, the basic structure of imidazopyridine is constructed.
Finally, the resulting imidazopyridine product is carboxylated. Select the appropriate carboxylation reagent and successfully introduce the carboxyl group at the target position in a suitable reaction environment to obtain 5-chloro-1H-imidazolo [4,5-b] pyridine-2-carboxylic acid. After each step of the reaction, appropriate separation and purification methods are required to ensure the purity of the product and improve the efficiency and quality of the synthesis.

I do not know the exact range of the market price of 5-chloro-1H-imidazolo [4,5-b] pyridine-2-carboxylic acid. Market prices often vary depending on the source, quality, purchase quantity and where and how they are sold. If you want to know the price, you should consult various chemical raw material suppliers, chemical trading markets, or explore online chemical product trading platforms. It may be quoted at the right price according to the quantity and quality you need. Or look at industry information, market survey reports, or get some information to know the approximate trend of the price of this product in the near future. However, I have not personally involved in market transactions, so it is difficult to determine its exact value. I only hope that this advice may be beneficial to your bid.

5-Chloro-1H-imidazolo [4,5-b] pyridine-2-carboxylic acid is a safety concern and requires attention to many aspects.
This compound has potential chemical activity and its toxicity should not be underestimated. When handling, be sure to wear appropriate protective equipment, such as protective clothing, gloves, and goggles, to prevent it from coming into contact with the skin and eyes, which may cause damage to human tissue.
During use, ventilation is essential. It needs to be operated in a well-ventilated place, and the best choice is in a fume hood, so as to avoid the accumulation of its volatile gaseous substances in a limited space, thereby reducing the risk of inhalation, in order to prevent irritation to the respiratory tract, severe cases or damage to lung function.
Furthermore, proper disposal of this substance is also extremely critical. Its waste must not be discarded at will, and must follow relevant regulations and standards, and be treated in a special way to prevent pollution of the environment, especially soil, water sources, etc., because of its chemical properties or long-term and complex effects on the ecosystem.
In addition, storage is also important. It should be stored in a dry, cool place away from sources of ignition and oxidants. Due to its chemical structure, it may be flammable or may react violently with oxidants. Standardized storage can avoid major safety accidents such as fire and explosion.
When operating and using 5-chloro-1H-imidazolo [4,5-b] pyridine-2-carboxylic acid, safety precautions at every step should not be ignored, so as to ensure that personnel safety and the environment are not endangered.