4(5)-imidazolecarboxaldehyde

4- (2- (5- (4- (2- (5-imidazole formaldehyde)) is an organic compound. This substance has a wide range of uses and is useful in various fields.
In the field of medicinal chemistry, it is often a key intermediate. A complex molecular structure with biological activity can be constructed through a series of chemical reactions. Due to the unique electronic properties and structure of the imidazole ring, the synthesized drug can precisely act on specific biological targets, or has various pharmacological activities such as antibacterial, antiviral, and antitumor. For example, some of the anti-cancer drugs developed on its basis can block the growth and proliferation signaling pathways of cancer cells by binding to specific proteins in cancer cells, and then achieve the effect of treating tumors.
In the field of materials science, it also has important uses. It can be used to prepare materials with special properties, such as optical materials and electrical materials. Because of its structure, it can participate in specific polymerization reactions to form polymer materials or composites. These materials may have excellent fluorescence properties and can be used in optical sensors to achieve highly sensitive detection of specific substances; or have good electrical properties, and have emerged in the field of electronic device manufacturing.
In the field of coordination chemistry, 4- (2- (5-imidazole formaldehyde can be used as a ligand to coordinate with metal ions to form a variety of coordination compounds. These coordination compounds exhibit unique physical and chemical properties due to the synergistic effect between metal ions and ligands, such as magnetism and catalytic activity. In the field of catalysis, some coordination compounds can be used as efficient catalysts to accelerate specific chemical reactions, and have high selectivity and stability, with great potential for industrial applications such as organic synthesis.

4 - (2 - (5 - ） - imidazole formaldehyde, the physical properties of this substance are particularly important, related to its use and characteristics.
Its color state is often white to light yellow crystalline powder, which is fine in appearance and uniform in texture. This color state is easy to identify and distinguish in various scenarios. In terms of solubility, it is slightly soluble in water, but soluble in organic solvents such as ethanol and dichloromethane. This property determines its dispersion and reaction behavior in different solvent systems, and is of great significance in chemical synthesis and preparation.
Its melting point is also a key property, and it is about a specific temperature range. This value can be used as a criterion for material purity and stability. The stable melting point indicates that the material structure is regular, the purity is high, and the stability is good; if the melting point fluctuates, the impurity or structural variation needs to be checked in detail.
Furthermore, its density also has characterization value. Although the value is specific, it has a great impact on material preparation and process design. Appropriate density can ensure the uniformity and fluidity of materials under specific process conditions, and plays an important role in product quality and production efficiency.
The physical properties of 4 - (2 - (5 - ） - imidazole formaldehyde are interrelated, and together form the cornerstone of its material characteristics, providing a basis for its application in chemical, pharmaceutical and other fields. Practitioners must consider it carefully to make good use of it.

4 - (2 - (5 - ） - imidazole formaldehyde, the chemical properties of this substance are as follows:
It has the typical properties of an aldehyde group. The aldehyde group is active and easy to oxidize. In case of weak oxidants such as Torun reagent, it can be oxidized to carboxylic acid, and at the same time, a silver mirror is formed. This is the famous silver mirror reaction, whereby the presence of aldehyde groups in the compound can be detected. When reacted with Feilin reagent, it can also be oxidized to produce a brick-red cuprous oxide precipitation.
In the reduction reaction, the aldehyde group can be reduced to a hydroxyl group by means of a suitable reducing agent, such as sodium borohydride, etc., to obtain the corresponding alcohol compound.
In addition, aldehyde groups can be added to compounds containing active hydrogen. For example, under acid catalysis with alcohols, hemiacetals and acetals can be formed. The aldehyde groups in 4 - (2 - (5 - ） - imidazole formaldehyde also have this reaction activity, which can be condensed with alcohols to form acetal products with specific structures. This reaction is often used in organic synthesis to protect aldehyde groups or construct complex organic structures.
And because its molecule contains imidazole rings, imidazole rings have certain basicity and coordination ability. The lone pair electrons on the nitrogen atom of the imidazole ring can coordinate with metal ions to form metal complexes, which show unique physical and chemical properties and may have potential applications in catalysis, materials science and other fields. At the same time, the hydrogen atoms on the ring can participate in electrophilic substitution reactions. Under appropriate conditions, various substituents can be introduced, and then a variety of compounds can be derived, enriching their chemical properties and application fields.

The synthesis method of 4 - (2 - (5 - ） - imidazole formaldehyde, although this substance is not directly described in ancient books, can be deduced according to chemical reasons.
Take imidazole as the base first, based on its nitrogen atom activity, or can react with suitable aldehyde-based reagents. For example, using halogenated aldehyde as the raw material, in a suitable solvent, such as dichloromethane, N, N-dimethylformamide, etc., add an appropriate amount of base, such as potassium carbonate, triethylamine, etc., to adjust the pH of the reaction environment, and the halogenated aldehyde and imidazole undergo nucleophilic substitution. When the halogen atom leaves, the aldehyde group is connected to a specific position of imidazole, or the target product can be obtained.
Or it can be converted from imidazole derivatives through functional groups. For example, groups that can be converted into aldehyde groups are introduced first, such as cyano, alcoholic hydroxyl, etc. If cyano is introduced, the cyano group can be converted into aldehyde group by hydrolysis under the catalysis of acid or base; if it is an alcoholic hydroxyl group, it can be oxidized into aldehyde group by mild oxidation reaction, such as Dess-Martin reagent, Swern oxidation system, etc., to achieve the synthesis of 4- (2- (5 - ） - imidazole formaldehyde. The process of synthesis requires careful selection of raw materials and conditions, weighing the advantages and disadvantages of each method, in order to achieve efficient and pure synthesis.

I don't know what the price of 4- (2- (5-imidazolyl)) -imidazole formaldehyde is in the market. However, if you want to know its price, you can explore it from multiple sources.
First, you can consult the suppliers of chemical raw materials. The world's merchants are involved in the trading of various chemical products. If you visit a merchant specializing in these fine chemicals, you may get their price. Or go to the chemical raw material market in person and consult various stores; or on the Internet, find its business name, email, phone, etc., and ask for details of its price, as well as more discounts.
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Third, refer to academic literature and industry reports. In the literature and reports in the chemical field, there may be mention of the market conditions of this chemical. Although the price is not real-time, it may be used as a reference to know the approximate range and trend of its price.
But because I have not personally involved the market conditions, it is difficult to determine its current exact price. If you want to get a precise price, you can follow the above paths and explore it in detail.