2,6-bis((R)-4-methyl-4,5-dihydrooxazol-2-yl)pyridine

2%2C6-bis%28%28R%29-4-methyl-4%2C5-dihydrooxazol-2-yl%29pyridine, this is the name of an organic compound. Its main use covers the field of organic synthesis and catalysis, and has a very important position.
In organic synthesis, this compound is often used as a ligand. Ligands can be combined with metal ions to form metal complexes. These metal complexes can show excellent catalytic properties in many organic reactions. For example, in some coupling reactions, such as Suzuki reaction, Heck reaction, etc., the metal complexes formed by it can effectively promote the reaction, improve the efficiency and selectivity of the reaction. Due to its special structure, it can coordinate with metal ions in a specific way, thus precisely regulating the electron cloud density and spatial environment of metal ions, and promoting the reaction to occur in the desired direction.
In the field of catalysis, it also plays a key role. With its unique structure and electronic properties, it can activate substrate molecules and reduce the activation energy of the reaction. In this way, many reactions that were originally difficult to occur can also be carried out smoothly under its catalysis. Not only that, its catalytic activity and selectivity are often better than other ordinary ligands or catalysts. This makes it possible to construct the structure of the target molecule more efficiently and accurately during the organic synthesis process, reduce the occurrence of side reactions, and improve the purity and yield of the product.
In short, 2%2C6-bis%28%28R%29-4-methyl-4%2C5-dihydrooxazol-2-yl%29pyridine plays an indispensable role in the field of organic synthesis and catalysis with its unique structural characteristics, which has greatly promoted the development and progress of related fields.

2%2C6-bis%28%28R%29-4-methyl-4%2C5-dihydrooxazol-2-yl%29pyridine, there are various methods of synthesis. One method can be started from the raw material containing pyridine. The pyridine derivative is first taken, and a specific group is introduced at the 2,6 position through a suitable reaction. This process requires delicate steps and rigorous conditions.
To introduce the desired ((R) -4-methyl-4, 5-dihydrooxazol-2-yl) group at the 2,6 position of pyridine, the nucleophilic substitution reaction is often used. An active ((R) -4-methyl-4, 5-dihydrooxazol-2-yl) reagent can be prepared first, and it can be reacted with the pyridine derivative under a suitable base and solvent environment. The base can help the reagent to generate nucleophilic species, and the solvent affects the rate and selectivity of the reaction. < Br >
Or the reaction path can be catalyzed by metals. For example, using transition metal catalysts, such as palladium, nickel, etc., to couple pyridine derivatives with halogenated or halogenated compounds containing (R) -4-methyl-4, 5-dihydrooxazol-2-yl). This path requires precise control of the amount of catalyst, reaction temperature and time. If the temperature is too high or the time is too long, side reactions may occur and the product is impure.
Furthermore, from the perspective of constructing a pyridine ring, pyridine is formed by cyclization of raw materials containing corresponding substituents, and the desired ((R) -4-methyl-4, 5-dihydrooxazol-2-yl) structure is constructed at 2,6 positions. This strategy requires clever design of the structure and reaction conditions of the raw materials to achieve efficient synthesis of the target product. The synthesis process requires careful observation of the mechanism and conditions of each step of the reaction, and careful operation to obtain pure 2%2C6-bis%28%28R%29-4-methyl-4%2C5-dihydrooxazol-2-yl%29pyridine products.

2%2C6-bis%28%28R%29-4-methyl-4%2C5-dihydrooxazol-2-yl%29pyridine, this is an organic compound. Its physical properties are very important, and it is related to its performance in various chemical processes and practical applications.
Looking at its properties, under normal temperature and pressure, or as a solid state, it has a specific crystal structure. This crystal form has a great influence on its stability and many physical properties. Its melting point is the critical temperature at which a substance changes from a solid state to a liquid state. The exact value can be obtained by experimental measurement. This value is critical when identifying and purifying the compound.
Furthermore, solubility is also an important property. In common organic solvents, such as ethanol, dichloromethane, etc., the degree of solubility varies. In polar solvents, or due to intermolecular forces, it exhibits a certain solubility, which is extremely important for its participation in solution-phase chemical reactions or as a solute preparation solution.
The density of the compound reflects the mass per unit volume. When mixed with other substances, the density factor affects the phase distribution and flow properties of the system.
In addition, its volatility cannot be ignored. Although the degree of volatilization at room temperature may not be high, the change of the volatilization rate may affect its storage and use under heating or specific environments. < Br >
And the color and odor of the compound, although not the key distinguishing properties, are also part of its physical characteristics, or colorless and odorless, or have a weak color and odor, which can provide some clues for preliminary judgment.
In short, 2%2C6-bis%28%28R%29-4-methyl-4%2C5-dihydrooxazol-2-yl%29pyridine physical properties are diverse and interrelated, and in-depth understanding of these properties can make better use of this compound in chemical research and industrial production.

2% 2C6 - bis% 28% 28R% 29 - 4 - methyl - 4% 2C5 - dihydrooxazol - 2 - yl% 29pyridine, this is an organic compound. It has the following chemical properties:
1. ** Coordination characteristics **: This compound contains nitrogen heterocycles and chiral oxazoline structures. The nitrogen atoms on the pyridine ring and the oxazoline ring have lone pair electrons, which can act as ligands to coordinate with metal ions. If complexed with transition metal ions, it forms metal complexes, which show unique properties in the field of catalysis. Due to the chiral oxazoline structure giving it a chiral environment, the formed complex may have chiral recognition and asymmetric induction ability. In asymmetric catalytic reactions, such as asymmetric hydrogenation, epoxidation and other reactions, it can efficiently generate products of specific configurations. It has a wide range of uses in the field of drug synthesis and total synthesis of natural products.
2. ** Basic **: Pyridine cyclic nitrogen atoms have lone pairs of electrons, making the compound alkaline to a certain extent. It can accept protons in solution and react with acids to form salts. This basic property affects its existence form and chemical activity under different acid-base conditions. In organic synthesis, its alkaline catalysis can be used to catalyze specific reactions, or as an acid binding agent to absorb the acid generated by the reaction to promote the positive progress of the reaction.
3. ** Stability **: In its molecular structure, the pyridine ring and the oxazoline ring are connected by chemical bonds to form a relatively stable rigid structure. The aromatic ring conjugate system and the oxazoline ring structure endow the compound with certain thermal stability and chemical stability, and can exist stably under conventional conditions. However, under extreme conditions such as strong oxidants, strong acids, strong bases or high temperatures, its chemical bonds may be destroyed, causing structural changes and chemical reactions.
4. ** Solubility **: Since the molecule contains polar nitrogen atoms and organic groups, it has certain solubility in organic solvents, such as common dichloromethane, chloroform, toluene, acetonitrile, etc. However, due to the large molecule and certain hydrophobicity, the solubility in water is not good. This solubility property is of great significance in the synthesis, separation, purification and solvent selection of compounds.

I don't know the price of 2,6-bis ((R) -4-methyl-4,5-dihydrooxazole-2-yl) pyridine in the market. This is a fine chemical, and its price often varies depending on quality, purity, and supply and demand.
If it is a high-purity product used in high-end scientific research or pharmaceuticals, the price may be high. Because of the difficulty of preparation, it requires fine craftsmanship and harsh conditions, and the raw materials may be expensive. And if special packaging and transportation conditions are required to ensure its stability, the cost will also increase, and the price will rise accordingly.
If the market demand for this product is strong and the supply is limited, the price will also rise. On the contrary, if there is excess capacity and demand is flat, the price may stabilize or decline.
The pricing of different suppliers is also different. Large manufacturers may be cost-controllable due to economies of scale, and the price may be competitive; if small manufacturers focus on quality and research and development, the price may be higher.
However, we do not have the exact market information, so it is difficult to determine its specific price. To know the price of this product, you can consult chemical raw material suppliers, online chemical trading platforms, or consult relevant market survey reports to get near real-time prices.