7-methyl-2-[(pyrimidin-2-ylsulfanyl)methyl]imidazo[1,2-a]pyridine

7 - methyl - 2 - [ (pyrimidin - 2 - ylsulfanyl) methyl] imidazo [1,2 - a] pyridine is an organic compound. Its chemical structure is quite complex and consists of a clever combination of several parts.
Looking at its structure, the core part is the skeleton of imidazo [1,2 - a] pyridine. In this skeleton, the pyridine ring fuses with the imidazole ring to form a unique ring structure. At position 2 of the imidazo [1,2 - a] pyridine skeleton, a [ (pyrimidin - 2 - ylsulfanyl) methyl] group is connected. In this group, the pyrimidine-2-group is connected to the methylene through the sulfur atom, and then forms the phase of imidazolo [1,2-a] pyridine at position 2.
In addition, there is a methyl group at position 7 of the imidazolo [1,2-a] pyridine skeleton. The introduction of methyl groups changes the physical and chemical properties of the compound, such as its polarity and steric resistance.
Overall, the chemical structure of 7 - methyl - 2 - [ (pyrimidin - 2 - ylsulfanyl) methyl] imidazo [1,2 - a] pyridine is unique, and the interaction of various parts endows it with specific chemical and physical properties. It may be of important value in the fields of organic synthesis and medicinal chemistry.

7-Methyl-2- [ (pyrimidine-2-ylthio) methyl] imidazolo [1,2-a] pyridine, this is an organic compound, which has important uses in the fields of medicine, pesticides and so on.
In the field of medicine, it may be a potential drug intermediate. Drug intermediates are key raw materials or intermediates for the synthesis of drugs, and can be converted into drugs with therapeutic effect through specific chemical reactions. The special structure of this compound may endow it with the ability to bind to specific targets in organisms, such as certain enzymes, receptors, etc. By interacting with targets, or regulating physiological processes in organisms, the purpose of treating diseases can be achieved. For example, it can be used to develop anti-tumor drugs, which can play an anti-cancer role by interfering with the signaling pathway of tumor cells and inhibiting the proliferation and metastasis of tumor cells; or it can be used to develop drugs for the treatment of nervous system diseases, regulate the release and transmission of neurotransmitters, and improve nervous system function.
In the field of pesticides, it may be an important lead compound for the creation of new pesticides. The lead compound has specific biological activities, and after structural modification and optimization, it is expected to develop high-efficiency, low-toxicity, and environmentally friendly pesticide varieties. This compound may have specific biological activities for certain pests and pathogens, such as inhibiting the growth and development of pests and interfering with the metabolic process of pathogens, so as to achieve the control of pests and diseases. For example, it can be developed as an insecticide to target specific pests, such as aphids, planthoppers, etc., with efficient killing effect; or it can be developed as a fungicide to control fungal and bacterial diseases of crops and ensure crop yield and quality.
In summary, 7-methyl-2 - [ (pyrimidine-2-ylthio) methyl] imidazolo [1,2-a] pyridine has broad application prospects and potential value in the field of pharmaceutical and pesticide research and development.

To prepare 7-methyl-2 - [ (pyrimidine-2-ylthio) methyl] imidazolo [1,2-a] pyridine, the method is as follows:
First, imidazolo [1,2-a] pyridine is used as a group. Under specific reaction conditions, it can be reacted with methyl-containing reagents to introduce 7-methyl. This process requires temperature control, selection of suitable solvents and catalysts to promote the reaction in the desired direction. If a suitable halomethane is used as the methyl source, under the catalysis of a base, in an organic solvent, through nucleophilic substitution, the methyl group is connected to the 7 position of imidazolo [1,2-a] pyridine. [ (Pyrimidine-2-ylthio) methyl] needs to be introduced for
times. First, pyrimidine-2-mercaptan is taken and reacted with halogenated methyl reagents to obtain a halide containing [ (pyrimidine-2-ylthio) methyl]. The halide is then reacted with imidazolo [1,2-a] pyridine with 7-methyl. The two are nucleophilic substituted in a suitable solvent in the presence of a base to form the target product 7-methyl-2 - [ (pyrimidine-2-ylthio) methyl] imidazolo [1,2-a] pyridine. < Br > After the reaction is completed, the product needs to be separated and purified. According to the physical properties of the product and impurities, methods such as extraction, column chromatography, and recrystallization can be used. Extraction is carried out to separate the products in different solvent phases, column chromatography is separated by adsorption difference, and recrystallization is purified by solubility difference to obtain pure 7-methyl-2 - [ (pyrimidine-2-ylthio) methyl] imidazolo [1,2-a] pyridine.

7-Methyl-2- [ (pyrimidine-2-ylthio) methyl] imidazolo [1,2-a] pyridine is a kind of organic compound. In terms of physical and chemical properties, it has many characteristics.
Looking at its physical properties, under normal conditions, it may appear in a solid state, but the exact state depends on the surrounding environmental conditions. Its melting point and boiling point are both key parameters characterizing the physical properties of this substance. The melting point is the temperature at which the substance melts from solid to liquid. The melting point of this compound depends on the strength of intermolecular forces. If the intermolecular force is strong, more energy is required to break the lattice structure, and the melting point is high; otherwise, it is low. The boiling point is also the same, which is the temperature when the substance changes from the liquid state to the gaseous state, reflecting the energy required for the molecule to break free from the liquid phase.
As for the chemical properties, the functional groups such as pyrimidinyl, imidazopyridinyl and thiomethyl contained in this compound give it unique chemical activities. Pyrimidinyl and imidazopyridinyl are both rich in nitrogen atoms and have a certain alkalinity, which can react with acids to form corresponding salts. Sulfur atoms in thiomethyl groups, due to their outer electronic structure, are nucleophilic and can participate in nucleophilic substitution reactions. For example, it can react with halogenated hydrocarbons to generate new sulfur-containing compounds and expand the structure and function of the molecule. In addition, due to the existence of the conjugate system, this compound may have certain stability, but under specific conditions, such as high temperature, strong oxidants or reducing agents, the conjugate system may be destroyed, triggering chemical reactions, resulting in changes in the structure and properties of the compound.
Furthermore, in terms of solubility, because the molecule contains both polar parts of nitrogen-containing heterocycles and non-polar parts such as methyl groups, it may have a certain solubility in polar solvents such as alcohols and ketones, but in non-polar solvents such as alkanes, the solubility may be low. This solubility characteristic has an important impact on its chemical reaction, separation and purification, and practical application.

I have searched all over the market, but in today's world, 7 - methyl - 2 - [ (pyrimidin - 2 - ylsulfanyl) methyl] imidazo [1,2 - a] pyridine is rarely heard of, and the valence is geometric, and it is difficult to find its trace.
Looking at the name of this chemistry, its structure is complex, and it is not an ordinary thing to use. It is either used for subtle scientific research, or required for specific experiments. To a common sense, if it is a reagent customized by a scientific research institute, its price should vary according to the quantity and purity.
If it is of high purity, if it is taken in small amounts, it will be as expensive as gold. Due to the difficulty of preparation, the complexity of purification, and the huge cost of manpower and material resources. Or the price per gram, up to a hundred gold or even a thousand gold.
However, if it is mass-produced, and the purity requirements are slightly lower, for industrial preliminary exploration and the like, the price may be slightly reduced. However, it is also an unusual price, or tens of gold per gram.
But the market has not heard its voice, nor can it be seen, so it is difficult to determine its true price. Or you need to ask Jia people who specialize in chemical reagents, or ask Fangjia who studies chemistry in depth, to get a clue. Although I have the intention to ask for its price, the information is lacking, and it is difficult to tell accurately.