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What are the main uses of 2- (2-nitrophenyl) H-imidazolo [1,2-a] pyridine?
2- (2-hydroxyethyl) H-histamino [1,2-a] is mainly used in the field of medicine, especially in the research and treatment of diseases related to the nervous system.
This compound is useful for scientists to explore the mechanism of action of neurotransmitters in the study of the nervous system. It can mimic or modulate the activity of neurotransmitters, thus providing key clues for understanding the normal physiological functions of the nervous system and abnormal changes in disease states. For example, in the study of certain neurodegenerative diseases, such as Parkinson's disease and Alzheimer's disease, by studying the effect of this compound on nerve cell signaling, new therapeutic targets and therapeutic strategies are expected to be discovered.
In the field of medical treatment, 2- (2-hydroxyethyl) H-histamino [1,2-a] can be used as a potential drug lead compound. Drug developers have modified and optimized its structure based on its structure and activity characteristics, in order to develop new drugs with higher efficacy and lower side effects. It can specifically act on some receptors in the nervous system, thereby regulating the balance of excitability and inhibition of nerve cells, which is of great significance for alleviating the symptoms of nervous system diseases. For diseases such as migraine and epilepsy, this compound and its derivatives may be able to reduce symptoms and improve the quality of life of patients by regulating the neurotransmission process.
Furthermore, as an important tool compound in pharmacological research experiments, it can be used to evaluate the effects of other drugs on the nervous system. By observing the changes in the physiological function of nerve cells caused by other drugs in the presence or absence of this compound, we can gain a more comprehensive understanding of the interactions between drugs and the mechanism of action of drugs, providing a theoretical basis for clinical rational drug use.
What are the synthesis methods of 2- (2-nitrophenyl) H-imidazolo [1,2-a] pyridine
To prepare 2 - (2 - aminophenyl) H - indolo [1,2 - a] pyridine, there are many synthesis methods, each has its own advantages and disadvantages, and should be selected according to the specific situation.
First, 2 - (2 - aminophenyl) pyridine is obtained by the coupling reaction of o-bromoaniline and 2 - pyridyl boronic acid through palladium catalysis. Subsequently, the product is reacted with a suitable halogenated aromatic hydrocarbon under the co-assistance of base and palladium catalyst through molecular close ring reaction, and the target product can be obtained. The advantage of this approach is that the raw materials are easy to find, the reaction conditions are mild and controllable, and the yield is also considerable. However, the cost of palladium catalysts is high, the post-reaction treatment is complicated, and chromatographic column separation is required to achieve high purity.
Second, 2-halogenated pyridine and o-amino acetophenone are used as starting materials. The two are condensed in an alkaline environment to form an enamine intermediate. Then, by acid-catalyzed cyclization, it is converted to 2- (2-aminophenyl) H-indolo [1,2-a] pyridine. The advantage of this method is that the reaction steps are simple and convenient to operate. However, the acid-catalyzed cyclization step requires strict reaction conditions. A slight deviation in acidity and temperature affects the yield and product purity, and it is not easy to obtain some specific substituent derivatives of the starting material 2-halogenated pyridine.
Third, with o-nitroaniline and 2-pyridyl formaldehyde as the starting materials, it is first condensed to form Schiff base, and then reduced to 2- (2-aminophenyl) pyridine derivatives, which are then reacted into rings by similar molecular close rings. The advantage of this route is that the reducing agent used in the reduction step is relatively inexpensive. However, the reduction process needs to strictly control the conditions to prevent excessive reduction or other side reactions, and the nitro reduction process may have more impurities, which will add to the separation and purification. < Br >
When synthesizing 2- (2-aminophenyl) H-indolo [1,2-a] pyridine, factors such as raw material cost, reaction conditions, yield, purity and subsequent separation should be comprehensively considered to select the most suitable method.
What are the physicochemical properties of 2- (2-nitrophenyl) H-imidazolo [1,2-a] pyridine
(What are the physical and chemical properties of 2 - (2 - cyanobenzyl) H - pyridino [1,2 - a]?)
The properties of all things are determined by their structure and quality. Now there is (2 - (2 - cyanobenzyl) H - pyridino [1,2 - a]. If you want to understand its physical and chemical properties, let me tell you one by one.
First talk about its physical properties. Looking at its state, at room temperature, it is either a solid crystal, like a fine grain, translucent with light, or a viscous liquid, with a faint luster between the flows. As for the color, it may be colorless and transparent, as clear as water; it may also be light yellow, like the early morning light, light and elegant. Regarding its taste, get close to the smell, or there is a special smell, pungent and refreshing, or the breath is weak, you need to pay attention to it. Its melting point, due to the force between molecules, the melting point or in a specific temperature range, heated to that time, the state of matter changes from solid to liquid; the boiling point is higher, and it will turn into gaseous ascension. And its solubility, in organic solvents, may have different manifestations, in alcohol solvents, or soluble, forming a uniform liquid; in water, it may be insoluble, such as oil floating in water, distinct.
Re-state its chemical properties. This substance contains the structure of cyanogen and pyridine, and the cyanyl activity is quite strong, which is easy to participate in the reaction of nucleophilic substitution. In the case of nucleophilic reagents, the cyanyl carbon atoms are vulnerable to attack, and the replacement of groups occurs, thereby deriving new compounds. The pyridine and structure are aromatic, which makes its chemical properties stable and variable. In redox reactions, it can be used as a donor or recipient of electrons, depending on the reaction environment. In case of strong oxidizing agents, the pyridine ring may be oxidized, and the structure is changed; in case of reducing agents, electrons may be obtained and the structure is remodeled. And its nitrogen atom has a lone pair of electrons, which can complex with metal ions to form coordination compounds and exhibit different chemical activities.
This (2- (2-cyanobenzyl) H-pyridino [1,2-a] material has unique physical and chemical properties and may have extraordinary uses in many fields such as chemical industry and medicine.
What is the market price of 2- (2-nitrophenyl) H-imidazolo [1,2-a] pyridine?
Today there is a question, what is the price of 2- (2-aminopyridine) H-imidazolo [1,2-a] in the market? I should answer it with the ancient style of "Tiangong Kaiwu".
The price of various things in the world often depends on multiple ends. The price of this 2- (2-aminopyridine) H-imidazolo [1,2-a] product also follows this principle.
First look at its source, if it is easy to obtain and abundant in production, the price may be leveled. Such as the trees of the mountain forest, if the vast forest is formed, it is not difficult to cut, and its price will not be high. However, if this substance requires delicate techniques to harvest, and the raw materials are rare, such as the precious ore in the mountains, it is not easy to find, and it is even more difficult to refine, then the price will be high.
If you observe its use again, if it is of great use in various industries, such as salt seasoning, iron making utensils, which are urgently needed by people, then the price will be high. Suppose this 2- (2-aminopyridine) H-imidazole [1,2-a] can be an essential agent for medical prescriptions, treating diseases and saving people, which is related to life and death, and its price is not high? On the contrary, if it is of little use, but ordinary things, although there are none, the price will be low.
Furthermore, it depends on the supply and demand of the city. If the supply exceeds the demand, such as the valley of the autumn harvest, if the warehouse is full of profit, the price will fall; if the supply exceeds the demand, such as the grain of the famine, the price will rise. The change of the city is impermanent, and the price also fluctuates.
Therefore, if you want to know the price of 2- (2-aminopyridine) H-imidazolo [1,2-a], you must carefully investigate its source, its use, and its supply and demand. Without knowing all these reasons, it is difficult to determine the geometry of its price on the market.
What are the safety and toxicity of 2- (2-nitrophenyl) H-imidazolo [1,2-a] pyridine?
2-%282-%E7%A1%9D%E5%9F%BA%E8%8B%AF%E5%9F%BA%29H-%E5%92%AA%E5%94%91, this is a strange chemical substance. To discuss its safety and toxicity, it is necessary to consider many aspects in detail.
In terms of safety, due to its unique structure, it is difficult to determine its safety without detailed experimental investigation. If it is accidentally contacted with the human body, or causes skin allergies due to unique structures, or irritates mucous membranes, if it accidentally enters the eyes, it may cause eye discomfort, pain, or even damage vision. If it inhales its volatile components, or affects the respiratory tract, causing cough, asthma, etc. And in the environment, its stability is unknown, or reacts with other substances, posing a potential threat to the surrounding ecology.
When it comes to toxicity, it is speculated from the structure that 2-%282-%E7%A1%9D%E5%9F%BA%E8%8B%AF%E5%9F%BA%29H-%E5%92%AA%E5%94%91 nitrogen-containing and special group-containing structures may interfere with the normal biochemical reactions in organisms. At the cellular level, it may affect cell metabolism, division, and cell lesions. Long-term exposure, or such as chronic poisons, gradually damages the function of human organs, such as the liver, kidneys and other detoxification and detoxification organs bear the brunt, affecting the normal physiological functions of the human body.
However, the above are all speculations based on the chemical structure and characteristics of common chemicals. To determine its safety and toxicity, rigorous experiments are required. Professionals use scientific methods to test different organisms under different conditions and obtain accurate data before they can have a definite understanding of its safety and toxicity.