Tert-Butyl 5-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-3,4-Dihydropyridine-1(2H)-

Eh! Fu tert - Butyl + 5 - (4,4,5,5 - Tetramethyl - 1,3,2 - Dioxaborolan - 2 - Yl) - 3,4 - Dihydropyridine - 1 (2H) This substance has a wide main application field. In the field of organic synthesis, it is often used as a key intermediate. Due to its unique structure, the boron-containing part is linked to the pyridine ring, which can induce a variety of chemical reactions.
In organic synthesis, boron groups can be used to participate in coupling reactions, such as Suzuki-Miyaura coupling, which can efficiently form carbon-carbon bonds and play an important role in the construction of complex organic molecules. It helps chemists to prepare many bioactive compounds, natural product mimics, or precursors of new materials.
Furthermore, it can also be seen in the field of medicinal chemistry. Since the pyridine ring is a common structural unit of many drug molecules, the compound can be further modified and transformed to meet the needs of drug design, or to optimize the activity, selectivity, and pharmacokinetic properties of the drug. < Br >
And in the field of materials science, compounds derived from this raw material may endow materials with unique photoelectric properties. For example, the preparation of organic materials with specific luminescence or electrical conductivity may have potential applications in optoelectronic devices such as organic Light Emitting Diodes (OLEDs), organic solar cells, etc., providing new avenues for material innovation.

To prepare tert-butyl 5- (4,4,5,5-tetramethyl-1,3,2-dioxoboran-2-yl) -3,4-dihydropyridine-1 (2H), there are various methods. Common ones can first take suitable pyridine derivatives, modify them with specific reagents, and introduce suitable substituents into specific positions of the pyridine ring. This step requires precise control of reaction conditions, such as temperature, pH, etc., to prevent side reactions.
Then, the boron group part is introduced, often with boron-containing reagents, under the action of catalysts, reacts with precursor compounds to construct the dioxoboran ring structure. In this process, the choice of catalyst is crucial, and different catalysts can cause significant differences in reaction rates and yields.
In addition, the introduction of tert-butyl is also a key step. A suitable tert-butyl reagent can be selected and completed in a suitable reaction environment. After each step of the reaction, it needs to be separated and purified, such as column chromatography, recrystallization, etc., in order to obtain a high-purity target product. Every step requires caution before the synthesis of this compound can be achieved.

The name of this organic compound is "tert-butyl 5- (4,4,5,5-tetramethyl-1,3,2-dioxboron heterocyclopentane-2-yl) -3,4-dihydropyridine-1 (2H) -", and its physical and chemical properties are particularly important.
In terms of its physical properties, under normal circumstances, it may have a specific form, but its solid, liquid and gas states are not detailed. Its melting boiling point is related to practical applications. Although the value is not clear, the interaction of tert-butyl and dioxboron heterocyclopentane with dihydropyridine rings in the structure, or the melting boiling point is affected. Tert-butyl has a large steric resistance, or intermolecular forces change, which affects its phase transition.
Looking at its chemical properties, dioxyboron heterocyclopentanyl is active and can participate in a variety of reactions. It can be coupled with halogenated hydrocarbons, which is a common means of building carbon-carbon bonds. Pyridine ring is alkaline and can react with acid to form salts, changing its solubility and reactivity. The structure of 3,4-dihydropyridine also adds chemical activity, is easy to be oxidized, can participate in oxidation reactions, and change molecular structure and function.
Its solubility also needs to be considered. There are both lipophilic tert-butyl and carbon ring parts in the molecule, and boron-oxygen and other groups with certain polarity. It may have unique solubility in organic solvents and water, or it may be partially soluble in polar organic solvents, but its solubility in water is limited. This physicochemical property is of great significance in the fields of organic synthesis and drug development.

I see what you are asking about Tert - Butyl 5- (4,4,4,5 - Tetramethyl - 1,3,2 - Dioxaborolan - 2 - Yl) - 3,4 - Dihydropyridine - 1 (2H) in the market price range. However, the price of these compounds often varies for many reasons, which is difficult to determine.
First, the purity of this product is the key. If the purity is very high, it is almost flawless, and the price is high; if it contains impurities, the price is slightly lower. High purity is suitable for high-end scientific research experiments, and the price is high in scenes sensitive to impurities.
Second, the purchase quantity also affects the price. If you buy in large quantities, the merchant may give discounts due to the idea of small profits but quick turnover; if you only buy a little, the unit price may be high.
Third, the market supply and demand trend has a great impact. If there are many applicants, but there are few suppliers, the price will rise; on the contrary, if the supply exceeds the demand, the price will drop.
Fourth, the source of supply is also related. Different manufacturers set different prices due to different production processes and cost controls. Well-known large factories, with excellent craftsmanship and excellent product quality, the price may be high; small factories produce, the price may be competitive.
In summary, if you want to know the exact price range, you can get a more accurate figure by consulting the chemical supplier or the relevant trading platform. However, it is difficult for me to determine the number. I hope you can follow the above method and explore it yourself, and you can get satisfactory results.

Tert - Butyl 5 - (4, 4, 5, 5 - Tetramethyl - 1, 3, 2 - Dioxaborolan - 2 - Yl) - 3, 4 - Dihydropyridine - 1 (2H) This substance should be properly stored to ensure its integrity.
This medicine should be placed in a dry and cool place, protected from direct sunlight. Hot sunlight can make the composition of the medicine vulnerable and lose its original effect. In a dry place, it can prevent it from getting damp and mildew. If it is in a humid environment, the medicine is prone to spoilage and the efficacy is also damaged.
Temperature is also essential. It should be placed at room temperature, not near hot topics or too cold places. Hot topics can cause the substances in the medicine to evaporate and decompose; if it is too cold, it may change the shape and properties of the medicine, which is not conducive to the use of the medicine.
In addition, the storage of this material needs to be avoided by mixing with other things. Because of its nature or aggression with other things, a chemical reaction will occur and its quality will be damaged. When placed in a separate place, it should be kept in a sealed device to block the intrusion of external air, water vapor, etc. In this way, it can be properly stored to ensure that it can be used when it is used, and it can play its due effect.