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What is the chemical structure of 1H-Imidazole, 4- (2-ethyl-2, 3-dihydro-1H-inden-2-yl) -, monohydrochloride?
This is a chemical substance of 1H-imidazole, 4- (2-ethyl-2,3-dihydro-1H-indene-2-yl), monohydrochloride. To know its chemical structure, let me tell you in detail.
The core of this compound is an imidazole ring, which consists of two nitrogen atoms and three carbon atoms to form a five-membered heterocycle and has aromatic properties. Its No. 4 position is connected to a special group, namely 2-ethyl-2,3-dihydro-1H-indene-2-yl. The indenyl moiety, 2,3-dihydro-1H-indene is a fused ring structure, which is formed by fusing a benzene ring with a five-membered ring, and there is ethyl substitution at position 2. Furthermore, the presence of this compound in the form of a monohydrochloride salt means that there is a proton in its structure that forms a salt of the hydrochloride ion.
As shown in the diagram, the imidazole ring is pentagonal in shape, the two corners are nitrogen atoms, and the cotriangle is carbon atoms. Carbon at position 4 extends a chain and is connected to 2-ethyl-2,3-dihydro-1H-indene-2-yl. The hydrochloride part can be regarded as the combination of a hydrogen ion and the nitrogen atom on the imidazole ring, and the chloride ion is opposed to it to maintain the charge balance. In this way, it is the chemical structure of 1H-imidazole, 4- (2-ethyl-2,3-dihydro-1H-indene-2-yl), and monohydrochloride.
What are the physical properties of 1H-Imidazole, 4- (2-ethyl-2, 3-dihydro-1H-inden-2-yl) -, monohydrochloride?
4- (2-ethyl-2,3-dihydro-1H-indene-2-yl) -1H-imidazole, monohydrochloride, this is an organic compound with specific physical properties. It is mostly solid at room temperature. Due to the imidazole and indenyl structure, the intermolecular force is complex, resulting in a high melting point, about 150-160 ° C. The substance has good solubility in organic solvents, such as common ethanol and dichloromethane. Because the molecule has a certain polarity, it can form a moderate interaction with organic solvents and is easy to dissolve. It also has a certain solubility in water, but it is slightly lower than that of organic solvents. < Br >
Looking at its appearance, it is mostly white to off-white crystalline powder, with uniform color and fine particles when pure. Due to the hydrochloride part, this substance is acidic and can react in acid-base environments. It has good stability and is not easy to decompose under normal storage conditions, but its structure may be damaged when it encounters strong oxidizing agents, strong acids and strong bases. It is widely used in the field of organic synthesis and is often used as an intermediate to participate in many chemical reactions, helping to build complex organic molecular structures.
What are the common uses of 1H-Imidazole, 4- (2-ethyl-2, 3-dihydro-1H-inden-2-yl) -, monohydrochloride?
1H-imidazole, 4- (2-ethyl-2,3-dihydro-1H-indene-2-yl) -, monohydrochloride, this is an organic compound. Its common use is mostly in the field of organic synthesis.
In organic synthesis, it is often used as a key intermediate. Due to its unique chemical structure, it can participate in various chemical reactions to build more complex organic molecular structures. For example, when constructing nitrogen-containing heterocyclic compounds, it can be reacted with other specific reagents to achieve the expansion and modification of the ring system, and then synthesize compounds with specific biological activities or functions. < Br >
And because of its basic nitrogen atom, it may also have applications in the field of catalysis. In some acid-base catalytic reactions, with its alkaline characteristics, it can promote the reaction progress, adjust the reaction rate and selectivity.
In addition, in view of the existence of indenyl in its structure, it endows it with certain spatial resistance and electronic effects, which may make a difference in the field of medicinal chemistry. Or it can be used to design and synthesize new drug molecules, and optimize the activity, selectivity and pharmacokinetic properties of drugs by modifying their peripheral substituents.
All these are the outline of their common uses. However, the specific application still needs to be considered and explored in detail according to the actual reaction conditions, target product requirements and other factors.
What are the synthesis methods of 1H-Imidazole, 4- (2-ethyl-2, 3-dihydro-1H-inden-2-yl) -, monohydrochloride?
The synthesis method of 4- (2-ethyl-2,3-dihydro-1H-indene-2-yl) -1H-imidazole monohydrochloride is known in the ancient book "Tiangong Kaiwu". Although the synthesis method of such compounds is not detailed, the wisdom of creation contained in it can provide ideas for today's synthesis.
To make this compound, you can first take appropriate starting materials, such as indene and imidazole compounds with corresponding substituents. According to the ancient technical thinking, when paying attention to the selection of raw materials, just like the ancient mining method, it is necessary to seek its purity. Indane compounds need to have a 2-ethyl-2,3-dihydro-1H-indene-2-yl structure, and there are few impurities, so they can be radicals.
In the reaction steps, modern organic synthesis methods can be used to compare the rigor of ancient processing methods. First, under appropriate reaction conditions, indene and imidazole compounds can be reacted, or catalyzed, such as the ancient method of alchemy with medicine, and a suitable catalyst is selected in this reaction to promote the bonding of the two. This reaction may require a specific solvent environment, such as the ancient wine brewing must require good wine water, and the synthesis also requires the selection of appropriate solvents to make the reaction smooth.
After indene is combined with imidazole, a salt reaction is performed to obtain monohydrochloride. This step also needs to be carefully controlled, such as the ancient method of seasoning, more than one point is too much, less than one point is not enough. Adjust the pH of the reaction system, so that the appropriate amount of hydrochloric acid is combined with the previous product, and the final product is 4- (2-ethyl-2,3-dihydro-1H-indene-2-yl) -1H-imidazole monohydrochloride. Every step of the reaction requires careful observation of its changes, and the patience and focus of the ancient method are used to ensure the purity and yield of the product.
1H-Imidazole, 4- (2-ethyl-2, 3-dihydro-1H-inden-2-yl) -, monohydrochloride What are the precautions during use?
1H-imidazole, 4- (2-ethyl-2,3-dihydro-1H-indene-2-yl), monohydrochloride. When using this product, many matters need to be paid attention to.
Bear the brunt, and safety is of paramount importance. This compound may be toxic and irritating, and may cause discomfort or even injury when it touches the skin, eyes or inhales its dust and vapor. Therefore, when operating, be sure to wear suitable protective equipment, such as gloves, goggles, gas masks, etc., to prevent contact and inhalation.
Furthermore, storage methods should not be ignored. It should be stored in a dry, cool and well-ventilated place, away from fire, heat and incompatible substances. Due to its chemical properties, improper storage or deterioration or dangerous reactions.
During use, precise control of the dosage is extremely critical. According to the specific needs of the experiment or production, it should be measured with the help of precise measuring tools to avoid excessive dosage deviation, affecting the expected effect, or even leading to adverse consequences.
Repeat, it is important to understand its chemical properties and reaction mechanism. Know the types and conditions of reactions it can participate in, so as to plan the steps reasonably during use to avoid improper operation causing the reaction to go out of control or generate harmful by-products.
In addition, after use, proper disposal of residues and waste should not be ignored. It is necessary to comply with relevant environmental regulations and laboratory regulations, and should not be discarded at will to prevent environmental pollution.