2 Pyridineacetic Acid 5 Trifluoromethyl
pyridine pyrrole pyrazine piperidine piperazine

2-pyridineacetic acid, 5-(trifluoromethyl)-

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    882781

    Chemical Formula C8H6F3NO2

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    Frequently Asked Questions

    As a leading 2-pyridineacetic acid, 5-(trifluoromethyl)- 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 physical properties of 2-pyridineacetic acid, 5- (trifluoromethyl) -
    2-Pyridyl acetic acid, 5 - (trifluoromethyl), is also an organic compound. Its physical properties are quite important and are related to many chemical and industrial uses.
    First of all, its appearance is usually white to off-white crystalline powder, which is easy to handle and use in many experiments and production processes. Its color is pure, which lays a good starting condition for subsequent reactions and applications.
    When it comes to the melting point, it is about a specific temperature range. This temperature characteristic is of great significance for the identification and purification of this substance. By accurately measuring the melting point, its purity can be judged. If impurities are mixed, the melting point will often change, or decrease, or the melting range will widen.
    Solubility is also a key physical property. In common organic solvents, such as ethanol, dichloromethane, etc., there is a certain solubility. This property makes it possible to choose an appropriate solvent to promote the reaction in chemical reactions according to the needs of the reaction. When dissolved in ethanol, a uniform solution can be formed, which is conducive to intermolecular interactions and reactions. In water, the solubility is relatively limited, and this difference has a significant impact on separation, purification, and reaction system design.
    Furthermore, its density is also a specific value. Density is crucial when dealing with operations such as material measurement, mixing, and phase separation. In the process of preparing a solution of a specific concentration or performing liquid-liquid extraction, its density needs to be precisely known to ensure the accuracy of the experiment or production operation.
    In addition, the compound may have a certain volatility. Although the volatility is not strong, some molecules will still escape to the gas phase under specific temperature and environmental conditions. This property needs to be considered during storage and use to avoid material loss due to volatilization or impact on the environment.
    In short, the physical properties of 2-pyridyl acetic acid, 5- (trifluoromethyl) are diverse and interrelated, and are of great significance in the fields of chemical research, drug synthesis, material preparation, etc. In-depth understanding and good use of these properties can better exert the value of this compound.
    What are the chemical properties of 2-pyridineacetic acid, 5- (trifluoromethyl) -
    5- (trifluoromethyl) -2 -pyridyl acetic acid, this is an organic compound. It has unique chemical properties, let me explain in detail.
    Looking at its structure, the pyridine ring is connected to the acetic acid group, and the trifluoromethyl group is introduced at the 5th position of the pyridine ring. This structure imparts many properties to the compound.
    In terms of physical properties, due to the presence of trifluoromethyl groups, this group has strong electronegativity and electron absorption, which changes the molecular polarity. Generally speaking, compounds containing such groups may have different solubility in organic solvents. Usually in polar organic solvents such as dichloromethane, N, N-dimethylformamide, the solubility is quite good, because the molecular polarity and solvent polarity are compatible with each other.
    In terms of chemical properties, the nitrogen atom of the pyridine ring has a solitary pair of electrons, making it weakly basic and can react with acids to form corresponding salts. And the electron cloud density distribution on the pyridine ring changes due to the electron-withdrawing effect of trifluoromethyl, resulting in a decrease in the electrophilic substitution reaction activity on the ring, especially near the 5- (trifluoromethyl) position, electrophilic reagents are more difficult to attack. The carboxyl group of the acetic acid group is acidic and can neutralize with the base to form the corresponding carboxylate. In addition, carboxyl groups can participate in many reactions, such as esterification reactions, with alcohols catalyzed by acids to form ester compounds.
    The chemical properties of 5- (trifluoromethyl) -2 -pyridyl acetic acid are due to its unique structure, and it has important uses in the field of organic synthesis. It can be used as a key intermediate for the preparation of more complex organic compounds.
    What is the common synthesis method of 2-pyridineacetic acid, 5- (trifluoromethyl) -
    The common synthesis methods of 5- (trifluoromethyl) -2 -pyridyl acetic acid are mainly based on the technique of chemical synthesis. There are many methods, which are described in detail below.
    First, a compound containing a pyridine structure is used as the starting material. First, take a pyridine with an appropriate substituent, and introduce a halogen atom at a specific position of the pyridine through a halogenation reaction. The halogenated atom can be bromine or chlorine, etc. The common halogenated reagents used are N-bromosuccinimide (NBS) or a combination of iron halide and halogen. The halogenated pyridine derivative is then reacted with a reagent containing trifluoromethyl. If Grignard's reagents such as trifluoromethyl magnesium halide are used in a suitable solvent such as tetrahydrofuran, under the protection of low temperature and inert gas, the nucleophilic substitution reaction occurs between the two, and the 5- (trifluoromethyl) pyridine derivative can be obtained. Thereafter, through a carboxylation reaction, carbon dioxide is used as the carboxyl source, and under the action of metal catalysts such as magnesium and lithium, the 2-position of the pyridine derivative is introduced into the carboxymethyl group to obtain 5- (trifluoromethyl) -2-pyridyl acetic acid.
    Second, pyridine-2-acetic acid is used as the base material. Using the activity check point of pyridine-2-acetic acid, the pyridine ring is modified first. An electrophilic substitution reaction can be used to introduce trifluoromethyl at the 5-position of the pyridine ring with suitable trifluoromethylation reagents, such as trifluoromethylsulfonic anhydride. This reaction requires suitable catalysts and reaction conditions. For example, under the catalysis of Lewis acid, it is carried out in an appropriate temperature and solvent. After fine regulation of the reaction process, the target product 5- (trifluoromethyl) -2-pyridine acetic acid can be obtained.
    Third, other heterocyclic compounds are used as starting materials, and the pyridine ring and the desired substituent are converted in multiple steps. The heterocyclic ring with a partial structure similar to the pyridine ring is first synthesized, and then the pyridine ring is formed by cyclization, rearrangement and other reactions. During the reaction process, trifluoromethyl and acetic acid groups are introduced in a timely manner. For example, by ingeniously designing the participation steps of fluorine-containing reagents and carboxylating reagents, the structure of the target molecule is gradually constructed, and finally the synthesis of 5- (trifluoromethyl) -2-pyridyl acetic acid is achieved. Although this approach is cumbersome, it is flexible and can be flexibly adjusted according to raw materials and actual needs.
    2-Pyridineacetic acid, 5- (trifluoromethyl) - in which areas is it used
    2-Pyridyl acetic acid, 5 - (trifluoromethyl), this substance is useful in many fields. In the field of medicine, it is the key raw material for the creation of new drugs. Because of its unique chemical structure, it has specific biological activities, or can be precisely combined with human biological targets, helping to develop anti-inflammatory, anti-tumor and other specific drugs. In the field of chemical synthesis, it is like a magic key that can open the door to the synthesis of many complex organic compounds. With its special functional groups, through ingenious chemical reactions, it can construct materials with novel structures and excellent properties, contributing to the research and development of new polymer materials. In the field of agriculture, it has also emerged. It can be used as the basis for the creation of new pesticides, relying on the regulation of specific biological activities to achieve precise insect control and disease treatment, and is environmentally friendly, in line with the current needs of green agriculture development. And because of its unique chemical properties in the reaction, it can provide new directions and ideas for chemical research, and light up a bright light on the road of scientific research and exploration, leading researchers to explore unknown chemical fields and explore more potential application values.
    What is the market price of 2-pyridineacetic acid, 5- (trifluoromethyl) -?
    2-Pyridineacetic acid, 5- (trifluoromethyl) - that is, 5- (trifluoromethyl) -2-pyridyl acetic acid. The market price of this compound is difficult to determine the exact value due to many factors.
    This compound may have applications in chemical and pharmaceutical research and development. In chemical synthesis, it can be used as an intermediate for specific reactions to help form materials with special properties; in pharmaceutical research and development, it may be a key raw material for potential drug synthesis.
    Its price fluctuates, mainly due to supply and demand. If pharmaceutical companies are active in the research and development of new drugs containing this structure, the demand will increase sharply, and the price will rise; conversely, if the demand is weak, the price will stabilize or fall.
    Furthermore, the cost of raw materials has a great impact. The synthesis of 5- (trifluoromethyl) -2 -pyridyl acetic acid requires specific starting materials and reagents. If the cost of these raw materials increases due to scarcity of resources and limited production, the price of the product will also increase.
    The complexity of the production process is also critical. If the synthesis requires multi-step reactions, harsh conditions or special equipment, the production cost is high, and the market price is also high; if the process is improved, the cost will decrease, and the price may also decrease.
    In addition, market competition also plays a role. If there are many manufacturers and the competition is fierce, it is necessary to occupy the market or reduce the price for promotion; if there are few manufacturers, it is monopolistic and the price may be high.
    In summary, the market price of 5- (trifluoromethyl) -2 -pyridyl acetic acid is difficult to estimate with certainty, or fluctuates between tens of yuan and hundreds of yuan per gram, depending on the actual supply and demand, cost, and competition in the current market.