Competitive 5-Bromopyridine-2-Carboxylate prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365036030 or mail to
info@alchemist-chem.com.
We will respond to you as soon as possible.
Tel: +8615365036030
Email: info@alchemist-chem.com
As a leading 5-Bromopyridine-2-Carboxylate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the chemical properties of 5-Bromopyridine-2-Carboxylate?
5-Bromopyridine-2-carboxylic acid ester, this is one of the organic compounds. Its chemical properties are unique and of great research value.
From the structural point of view, the compound contains bromine atoms, pyridine rings and carboxylic acid ester groups. Bromine atoms can make molecules have certain polarity due to their high electronegativity, and bromine atoms are highly active, making them easy to participate in nucleophilic substitution reactions. In many organic synthesis reactions, bromine atoms can often be replaced by other functional groups, such as reacting with nucleophiles to form new carbon-heteroatom bonds, thereby constructing more complex organic molecular structures.
Pyridine rings are aromatic, and the electron cloud distribution is special, which endows molecules with certain stability. At the same time, there are lone pairs of electrons on the pyridine ring nitrogen atom, which can be used as electron donor to participate in the coordination reaction and form complexes with metal ions, which has potential applications in the field of catalysis.
Carboxylate groups endow molecules with hydrolytic properties. Under acidic or basic conditions, 5-bromopyridine-2-carboxylic acid esters can undergo hydrolysis reactions. In acidic hydrolysis, 5-bromopyridine-2-carboxylic acid and corresponding alcohols are formed; in basic hydrolysis, carboxylic salts and alcohols are formed. This hydrolysis reaction is often used in organic synthesis to prepare carboxylic acids or their derivatives.
In addition, the functional groups in 5-bromopyridine-2-carboxylic acid esters The conjugation of bromine atom and pyridine ring will affect the electron cloud density of pyridine ring, and then affect its electrophilic substitution and nucleophilic substitution reactivity. The conjugation of carboxylic acid ester groups with pyridine ring also affects each other's reactivity, and this interaction makes the compound exhibit various reaction paths and products in organic synthesis reactions.
What are the common synthetic methods of 5-Bromopyridine-2-Carboxylate?
The common synthesis methods of 5-bromopyridine-2-carboxylate are as follows:
First, pyridine is used as the starting material to take advantage of the reactivity characteristics of the pyridine ring. Under appropriate reaction conditions, the pyridine ring is brominated. Generally, suitable brominating reagents can be selected, such as liquid bromine. In the presence of appropriate catalysts (such as Lewis acids such as iron powder), electrophilic substitution reactions will occur on the pyridine ring. Due to the electron-withdrawing action of nitrogen atoms on the pyridine ring, the electron cloud density of the 2-position and 4-position is relatively low, and substitution reactions are more likely to occur. After optimization of conditions, the bromine atom can be mainly substituted at the 5-position to obtain 5-bromopyridine.
Then 5-bromopyridine is carboxylated. A common method is through the Grignard reagent method. 5-bromopyridine is reacted with magnesium in an inert solvent such as anhydrous ether to make Grignard reagent. This Grignard reagent has strong nucleophilicity, and then reacts with carbon dioxide gas at low temperature. Carbon dioxide acts as an electrophilic reagent to undergo nucleophilic addition with Grignard reagent. After the reaction is completed, the carboxyl group can be introduced at the 2-position of the pyridine ring to obtain 5-bromopyridine-2-carboxylic acid.
Finally, 5-bromopyridine-2-carboxylic acid and the corresponding alcohol are heated to carry out esterification reaction in the presence of a catalyst such as concentrated sulfuric acid. The type of alcohol determines the structure of the final 5-bromopyridine-2-carboxylic acid ester. 5-Bromopyridine-2-carboxylic acid was synthesized by dehydration and condensation of acid and alcohol to form ester bond. Precise control of reaction conditions and separation and purification of each step were needed to ensure the purity and yield of the product.
What are the main applications of 5-Bromopyridine-2-Carboxylate?
5-Bromopyridine-2-carboxylate, this substance has a wide range of uses and plays a key role in the field of pharmaceutical synthesis. Due to its unique structure, it can provide an important intermediate for the creation of new drugs. In the process of drug development, based on this, special chemical structures can be constructed to give drugs specific physiological activities.
In the field of materials science, 5-bromopyridine-2-carboxylate also has a place. It can participate in the preparation of functional materials, such as materials with special optical and electrical properties. By reacting with other compounds, it can regulate the microstructure of materials, thereby optimizing material properties and meeting the application needs of different scenarios.
In the field of organic synthetic chemistry, this compound is an important raw material and often appears in the construction process of complex organic molecules. With its bromine atom and carboxyl group activity, it can carry out a variety of chemical reactions, such as nucleophilic substitution, esterification and other reactions, which help to synthesize complex organic compounds and contribute to the development of organic synthetic chemistry. In short, 5-bromopyridine-2-carboxylate plays an indispensable role in many fields such as medicine, materials, and organic synthesis, promoting technological progress and innovation in various fields.
What is the market price of 5-Bromopyridine-2-Carboxylate?
5-Bromopyridine-2-carboxylic acid ester, what is the price of this substance in the market? To know the details, you need to understand all the reasons. First, the purity of this compound is very important. If the purity is high and there are few impurities, the price must be high; if the purity is low and there are many impurities, the price may be low. Second, the difficulty of preparation also affects. If the preparation process is complicated, requires many steps, special reagents and conditions, the cost is high, and the price is also high; if the preparation is relatively simple, the price may be slightly lower. Third, the market supply and demand relationship affects the price. If there are many applicants and there are few suppliers, the price will rise; if the supply exceeds the demand, the price will tend to decline.
In addition, its packaging specifications are also related to the price. For large packages, the unit price may be low; for small packages, the unit price may be high due to the cost of sub-packaging, etc. And different merchants have different pricing due to their own cost considerations and marketing strategies. Some merchants focus on small profits but quick turnover, with slightly lower pricing; some focus on quality and brand, and their pricing may be high.
In the chemical raw material market, the price of such fine chemicals often changes from time to time. Raw material price fluctuations, production process improvements, and policy and regulatory impacts can all cause their prices to fluctuate. Therefore, in order to determine the market price of 5-bromopyridine-2-carboxylate, it is necessary to carefully investigate various factors in the current market, or consult chemical raw material suppliers and traders to obtain more accurate price information.
What are 5-Bromopyridine-2-Carboxylate storage conditions?
5-Bromopyridine-2-carboxylate is one of the chemical substances. Its storage conditions are crucial and related to the stability and quality of the substance.
This substance should be stored in a cool place to avoid high temperature roasting. High temperature can easily cause its chemical properties to change, causing decomposition or other adverse reactions. A cool place can keep its molecular structure stable. If it is a cool cellar, the temperature can often be maintained in a suitable range.
A dry place is also necessary for storage. Moisture is easily invaded and the substance is damp. If 5-bromopyridine-2-carboxylate is damp or reacts with water, the purity will be reduced and the quality will be damaged. Therefore, it needs to be placed in a dry environment, which can be assisted by desiccant to absorb the surrounding moisture.
Furthermore, sealed storage is indispensable. Exposed to air, it is easy to interact with oxygen, carbon dioxide and other components in the air. A sealed device, such as an airtight bottle, can block external gas interference and keep the substance as pure as ever.
In addition, the storage place should be away from fire sources and strong oxidants. This substance may be flammable or may react with oxidants. If the fire source is close, it may cause combustion or even explosion; if the strong oxidant encounters it, it may cause violent chemical reactions and cause safety accidents.
In short, 5-bromopyridine-2-carboxylate storage needs to be cool, dry, sealed, and protected from fire sources and strong oxidants, so as to maintain its quality for long-term use.