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6-Bromopyridine-2-Carboxylic chemical properties of Acid Methyl Ester
6-Bromopyridine-2-carboxylic acid methyl ester is one of the organic compounds. Looking at its chemical properties, this compound contains bromine atoms, pyridine rings and carboxylic acid methyl ester groups, and various functional groups give it unique chemical activities.
Let's talk about bromine atoms first, which have high electronegativity and are often used as good leaving groups for nucleophilic substitution reactions in chemical reactions. In the presence of suitable nucleophiles, bromine atoms can be replaced by other groups, such as by hydroxyl groups to form corresponding alcohol derivatives, or by amino groups to obtain nitrogen-containing derivatives. This property is of great significance in the field of drug synthesis and materials science, whereby complex organic molecular structures can be constructed.
Pyridine rings give this compound a certain alkalinity. The solitary pair of electrons on the nitrogen atom of the pyridine ring accepts protons, so that it can form pyridine salts in acidic media. And the electron cloud distribution of the pyridine ring is special, which affects the activity of surrounding groups, such as making the activity of the bromine atom connected to it different from that of the bromine atom in ordinary halogenated hydrocarbons. In addition, the pyridine ring is also an important pharmacophore, playing a key role in many drug molecules, affecting the biological activity and pharmacological properties of compounds.
Looking at the carboxylic acid methyl ester group, this functional group can undergo hydrolysis reaction. Under acidic or basic conditions, the ester bond is broken to form 6-bromopyridine-2-carboxylic acid and methanol. Basic hydrolysis is usually more complete, because the carboxylate formed is more stable. At the same time, methyl carboxylate can participate in the transesterification reaction, and exchange alkoxy groups with different alcohols under the action of catalysts to obtain ester derivatives with diverse structures, providing a rich way for organic synthesis.
In short, methyl 6-bromopyridine-2-carboxylate exhibits diverse chemical properties due to the interaction of functional groups, and has broad application prospects in organic synthesis, drug development and other fields.
6-Bromopyridine-2-Carboxylic Acid Methyl Ester
The synthesis method of methyl 6-bromopyridine-2-carboxylate has been explored by many parties throughout the ages. There are three methods, which can be described in detail.
First, 6-bromopyridine-2-carboxylic acid is used as the starting material. The acid is first mixed with methanol, and sulfuric acid is used as the catalyst to heat and reflux. During this period, the acid and alcohol undergo esterification reaction, and the reaction is fully carried out by condensation and reflux. After the reaction is completed, the reaction solution is cooled, neutralized to neutral in sodium bicarbonate solution, and then extracted with an organic solvent. The organic phase is dried with anhydrous sodium sulfate and distilled under reduced pressure to obtain methyl 6-bromopyridine-2-carboxylate. This is the classic esterification reaction path, which is relatively simple to operate and the raw materials are easy to obtain.
Second, 2-methyl-6-bromopyridine is used as the starting material. First, a strong oxidant, such as potassium permanganate, oxidizes the methyl group to a carboxyl group to obtain 6-bromopyridine-2-carboxylic acid. Then, according to the above esterification reaction method, it is reacted with methanol, and after a series of post-treatments, the final target product is obtained. Although this path has a little more steps, it is a good strategy for those who have abundant sources of specific raw materials.
Third, halopyridine derivatives are used as raw materials. Carboxyl methyl ester groups are introduced through suitable nucleophilic substitution reactions. For example, 6-bromo-2-halopyridine reacts with nucleophilic reagents containing carboxyl methyl esters at suitable temperatures in the presence of suitable bases and solvents. After the reaction is completed, 6-bromo-pyridine-2-carboxylic acid methyl ester can be obtained through separation and purification. The key to this method is the choice of nucleophilic reagents and reaction conditions to ensure the selectivity and yield of the reaction.
All synthesis methods have their own advantages and disadvantages, depending on the availability of raw materials, the difficulty of reaction conditions, and the requirements for product purity.
What are the main uses of 6-Bromopyridine-2-Carboxylic Acid Methyl Ester?
Methyl 6-bromopyridine-2-carboxylate has a wide range of uses. In the field of pharmaceutical synthesis, it is often used as a key intermediate. For example, when synthesizing drug molecules with specific structures, its pyridine ring and bromine and ester structures can participate in a variety of chemical reactions, borrowing nucleophilic substitution, coupling reactions, etc., to construct complex active molecular structures, help create new drugs, or optimize existing drug synthesis processes to improve yield and purity.
In the field of materials science, it also has its uses. Due to its unique structure, polymers can be chemically modified to impart special properties to materials, such as improving their optical and electrical properties. In the field of organic optoelectronic materials, Light Emitting Diodes, solar cells and other related materials can be prepared.
It is an important basic raw material in the study of organic synthetic chemistry. Researchers use its active functional groups to explore novel reaction paths and methodologies, expand organic synthesis strategies, and contribute to the development of organic chemistry. With its rich reactivity, many new organic compounds can be derived, opening up a broader space for chemical research.
6-Bromopyridine-2-Carboxylic Acid Methyl Ester when storing
Methyl 6-bromopyridine-2-carboxylate is an important raw material in organic synthesis. When storing, there are several points to be paid attention to.
Bear the brunt, and ensure that the storage environment is dry. This compound is susceptible to moisture, and humid environments are likely to cause hydrolysis. Once hydrolyzed, it will not only damage the purity of the compound, but also make it difficult to achieve the desired effect in subsequent synthesis reactions. Therefore, the storage place should be selected in a dry and ventilated place, and a desiccant can be placed as appropriate to absorb surrounding water vapor and maintain the environment dry.
Furthermore, temperature control is also crucial. Generally speaking, it should be placed in a cool place to avoid high temperatures. High temperature can easily make the chemical properties of the compound tend to be active, or cause adverse reactions such as decomposition and polymerization, thereby changing its chemical structure and properties. Generally, the suitable storage temperature is about - 20 ° C to 25 ° C, and different storage conditions may vary slightly due to specific requirements. Therefore, it is necessary to refer to the relevant instructions strictly.
In addition, methyl 6-bromopyridine-2-carboxylate is quite sensitive to light. Under light, it may cause luminescent chemical reactions and cause it to deteriorate. Therefore, dark bottles and cans should be used for storage containers to effectively block light and reduce the impact of light on them. If there is no dark container, the storage container can also be wrapped with opaque materials such as aluminum foil.
At the same time, the storage place must be kept away from dangerous items such as fire sources and oxidants. This compound may be flammable, and contact with oxidants may trigger a violent reaction, resulting in a safety accident. When storing, it is necessary to strictly follow the chemical storage specifications to reasonably separate it from other chemicals and avoid mutual influence.
Finally, it should be checked regularly during storage. Check the packaging for damage, signs of deterioration, etc. If any abnormalities are found, corresponding measures should be taken immediately, such as changing the packaging, disposing of spoiled items, etc., to prevent the problem from worsening and affecting the overall quality. In this way, it can ensure that methyl 6-bromopyridine-2-carboxylate maintains good quality during storage for subsequent use.
What is the market price range for 6-Bromopyridine-2-Carboxylic Acid Methyl Ester?
6-Bromopyridine-2-carboxylic acid methyl ester, the price of this product in the market is difficult to determine. The price of the cover often changes due to various reasons, and it cannot be generalized.
First, the price of raw materials is the main factor. The preparation of 6-bromopyridine-2-carboxylic acid methyl ester requires specific raw materials. If the production of raw materials changes, such as weather, geopolitics, and resource abundance, the price of raw materials will be affected. If raw materials are rare, the manufacturing cost will rise, and the price of 6-bromopyridine-2-carboxylic acid methyl ester will also be high; if raw materials are abundant and cheap, the price of the product may drop.
Second, the method of manufacturing is related to the cost. The quality of the process and the level of efficiency all affect the cost. Advanced and efficient methods may reduce energy consumption and yield, so that the cost can be controlled and the price can be stabilized or reduced; if the process is poor, the cost will increase and the price will be high.
Third, the supply and demand situation of the city is also the key. If the market demand for this product is strong, but the supply is limited, and the demand exceeds the supply, the price will rise; conversely, if the demand is low, the supply is excessive, and the supply exceeds the demand, the price will fall. And the state of industry competition also affects the price. The competition in the same industry is intense, or there are price cuts to compete for the market.
Fourth, external factors such as trade and tax policies cannot be ignored. The increase or decrease of tariffs and the establishment of trade barriers can cause changes in import and export costs, which in turn affect market prices.
In summary, the market price of methyl 6-bromopyridine-2-carboxylate often hovers within a certain range, but due to the intertwining of the above factors, it is difficult to determine its specific price range. To know the exact price, when you observe the market situation in real time, consult industry merchants or relevant suppliers, you can get a close-to-real number.