3 5 Dimethyl 1h Pyrrole 2 4 Dicarboxylic Acid 2 Tert Butyl Ester 4 Ethyl Ester
pyridine pyrrole pyrazine piperidine piperazine

3,5-dimethyl-1h-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester

    Specifications

    HS Code

    481920

    Chemical Formula C14H21NO4
    Molecular Weight 267.32
    Appearance Solid (predicted)
    Boiling Point Approximately 333.6 °C at 760 mmHg (predicted)
    Melting Point No specific experimental value found, but can be in a certain solid - state temperature range
    Solubility Soluble in organic solvents like dichloromethane, chloroform (predicted)
    Flash Point Approximately 155.5 °C (predicted)
    Density Around 1.07 g/cm³ (predicted)
    Pka No experimental pKa value found, but carboxylic acid groups can have pKa in the range of 3 - 5
    Ir Stretching Carbonyl stretches for ester and carboxylic acid groups around 1700 - 1750 cm⁻¹, C - H stretches around 2800 - 3000 cm⁻¹

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    General Information
    Where to Buy 3,5-dimethyl-1h-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester in China?
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    Frequently Asked Questions

    As a leading 3,5-dimethyl-1h-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester 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 3,5-dimethyl-1H-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester
    3% 2C5-dimethyl-1H-pyrrole-2% 2C4-dicarboxylic acid 2-pentene-4-acetamide is an organic compound with rich and unique chemical properties. It plays a key role in many chemical reactions and practical applications. Let me describe it in detail for you.
    This compound is acidic because its structure contains a carboxyl group. The carboxyl group can ionize hydrogen ions, develop acidic properties, and can neutralize with bases. In case of sodium hydroxide, it can form corresponding carboxylate and water. This is a common reaction of acid-base neutralization. It is often used in organic synthesis to adjust the pH of compounds and is also used for separation and purification of such compounds.
    It also has nucleophilic substitution activity. The hydrogen atom on the carbon atom at the ortho-position of the amide group and the carboxyl group has certain activity due to the influence of the carbonyl group. Under appropriate conditions, nucleophilic reagents such as halogenated hydrocarbons can attack this carbon atom and undergo nucleophilic substitution reactions. This is an important means to construct carbon-carbon bonds or carbon-hetero bonds. When synthesizing complex organic molecules, specific functional groups can be introduced to expand the structural diversity of the compound.
    In addition, the compound may have a conjugated system. Pyrrole rings are conjugated with dicarboxylic acids and other unsaturated bonds, resulting in special electronic effects and optical properties. The conjugated system can improve the stability of molecules, delocalize electron clouds, or affect their absorption spectra, which can be used in the field of materials science or can be used to prepare materials with specific optical properties, such as fluorescent materials.
    The existence of double bonds allows this compound to undergo an addition reaction. For example, under the action of hydrogen in a catalyst, the double bond can be hydrogenated and reduced to a single bond, which is a common method for preparing saturated compounds; it can also be added with halogens, hydrogen halides and other electrophilic reagents, introducing new functional groups at both ends of the double bond, enriching the chemical properties and uses of compounds, and is an important reaction path in the organic synthesis industry.
    In summary, the acidity, nucleophilic substitution activity, conjugation effect and double bond addition of 3% 2C5-dimethyl-1H-pyrrole-2% 2C4-dicarboxylic acid 2-pentene-4-acetamide make it have broad application prospects and research value in the fields of organic synthesis and materials science.
    What are the synthesis methods of 3,5-dimethyl-1H-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester
    In order to prepare 3 - (2,5 - dimethyl - 1H - pyrrole - 1 - yl) - 2,4 - dichlorobenzoic acid 2 - ethyl - 4 - methyl ester, there are many ways to synthesize it, which are described in detail as follows:
    The starting material can be selected from pyrrole derivatives and benzoic acid derivatives of the corresponding substituents. One method is to first substitution 2,5 - dimethyl pyrrole at 1 position with appropriate reagents, introduce suitable leaving groups, and then carry out nucleophilic substitution reactions with substrates containing 2,4 - dichlorobenzoic acid structures. This process requires careful selection of reaction conditions, such as reaction temperature, type and amount of solvent and base, to ensure that the reaction proceeds smoothly in the desired direction.
    The benzoic acid derivative can be modified first, introducing chlorine atoms at the 2,4 positions on the benzene ring, and introducing suitable protective groups at the carboxyl group. At the same time, the pyrrole derivative is activated to make the 1 position more reactive. Subsequently, the two are connected through a condensation reaction, and the protective group is finally removed to obtain the target product. In this path, the selection of the protective group is the key, which must not only ensure the stability of the carboxyl group during the reaction process, but also be easily removed at an appropriate stage.
    Furthermore, the strategy of gradually building the ring system can be adopted. First, pyrrole ring was constructed by multi-step reaction with small molecule raw materials, and 2,5-dimethyl substituent was introduced on it, and a fragment containing 2,4-dichlorobenzoate ethyl ester structure was constructed. Then, the two are connected by cyclization reaction to achieve the synthesis of the target product. This method requires precise control of the structure and reactivity of the reaction intermediate, and the reaction conditions of each step also need to be carefully optimized.
    Synthesis of 3- (2,5-dimethyl-1H-pyrrole-1-yl) -2,4-dichlorobenzoic acid 2-ethyl-4-methyl ester, or direct substitution from raw materials, or through the strategy of protecting groups, or gradually constructing ring systems, all need to be based on the actual situation, weigh the advantages and disadvantages of each method, and fine-tune the reaction conditions to achieve the purpose of efficient synthesis.
    What is the main use of 3,5-dimethyl-1H-pyrrole-2,4-dicarboxylate 2-tert-butyl ester 4-ethyl ester
    3% 2C5-dimethyl-1H-pyrrole-2% 2C4-dicarboxylic acid 2-ethyl-4-methyl ester has a wide range of main uses.
    In the field of pharmaceutical chemistry, this compound is often a key intermediate. Due to its special molecular structure, many biologically active substances can be derived by organic synthesis. For example, some drug molecules with specific pharmacological activities can achieve the expected structure and function through ingenious reaction pathways, using it as the starting material, and modifying it through multi-step reactions. This provides the possibility for the development of new drugs and helps to explore new drugs for treating diseases.
    In the field of materials science, it also has potential value. It may be able to participate in the construction of polymer materials with specific properties. Because of the characteristics of some functional groups in the structure, it may endow materials with unique physical and chemical properties, such as improving the stability and solubility of materials, and even endowing them with special properties such as optics and electricity, which contributes to the creation of new functional materials.
    Furthermore, in the study of organic chemistry, this compound is also an important research object. Chemists can gain insight into the mechanism of related chemical reactions, expand the type and scope of organic reactions, deepen the understanding and cognition of the basic principles of organic chemistry, and promote the development of organic chemistry. From this perspective, 3% 2C5-dimethyl-1H-pyrrole-2% 2C4-dicarboxylic acid 2-ethyl-4-methyl ester has important uses in many fields and is an indispensable part of scientific research and related industrial development.
    What is the market price of 3,5-dimethyl-1H-pyrrole-2,4-dicarboxylate-tert-butyl-4-ethyl ester?
    I have heard your inquiry about the market price of 3% 2C5-dimethyl-1H-pyrrole-2% 2C4-dicarboxylic acid 2-butyl-4-ethyl ester. However, it is not easy to know the market value of this product, and its price often varies due to many reasons.
    First, the origin and quality of the material have a great impact on its price. If the raw materials of this product are easy to harvest and of high quality, the cost of production may be slightly reduced, and the price will also be reduced; conversely, if the raw materials are rare or need to be refined, the price will rise.
    Second, the supply and demand of the city is also the key. If there are many buyers of this product in the city, but there are few suppliers, the price will increase; if the supply exceeds the demand, merchants may reduce the price in order to sell their goods.
    Third, the skills and labor costs of making this product are also related to its price. If there are new technologies that make it easy and cost-effective, the price may be reduced; if the system is complicated and the labor costs are numerous, the price will be difficult to lower.
    Fourth, the difference between time and place can also lead to changes in price. At different times, taxes, freight, etc. may be different; in different places, the supply, demand, and cost also vary, all of which can make the price difference.
    From this perspective, if you want to know the exact price of 3% 2C5-dimethyl-1H-pyrrole-2% 2C4-dicarboxylic acid 2-butyl-4-ethyl ester, you must carefully examine the raw materials, supply and demand, technology, time and place, etc., or consult the people in the industry and the brokers in the market, you can get a more accurate number.
    Precautions for storage and transportation of 3,5-dimethyl-1H-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester
    3% 2C5-dimethyl-1H-pyrrole-2% 2C4-dicarboxylic acid 2-pentene-4-ethyl ester is used in storage and transportation. When using the classical Chinese words of "Tiangong Kaiwu", it is necessary to pay attention to various things. The details are as follows:
    First environment. This material may be sensitive to changes in temperature and humidity. When storing, it is advisable to choose a cool, dry and well-ventilated place. If the humidity is too high, or it causes chemical changes such as hydrolysis, it will damage its quality. Remember the saying of "Tiangong Kaiwu" to store objects, to be dry, this also applies to this object. During transportation, it is also necessary to prevent the intrusion of external moisture, and moisture-proof materials can be used in the vehicle.
    Times and temperature. High temperature may cause it to decompose or cause other adverse reactions. When storing, the temperature should be controlled within a specific range and should not be overheated. During transportation, if it passes through a hot place, it is necessary to have a cooling strategy, such as using ice packs or refrigeration equipment to adjust the temperature to ensure its stability and not change due to heat.
    Furthermore, avoid touching impurities. This thing should be separated from other chemicals during storage and transportation to prevent mutual reaction. "Tiangong Kaiwu" discusses the harm of coexistence of various things, impurities or their qualitative change. Therefore, the container must be clean and well sealed to prevent external impurities from mixing.
    Repeat, the packaging is stable. Vibration and collision are inevitable during transportation, and poor packaging is prone to leakage. The packaging material is selected to be tough and impact-resistant, and ensure that it is tightly sealed. When storing, it is also necessary to prevent the container from being damaged and leaking.
    Also, the logo is clear. In the storage place and on the transportation vehicle, the name, nature, hazard and emergency treatment of this object should be clearly marked. Make it clear to the relevant parties at a glance. In case of an emergency, appropriate measures can be taken quickly to avoid major disasters.
    In summary, the storage and transportation of 3% 2C5-dimethyl-1H-pyrrole-2% 2C4-dicarboxylic acid 2-pentene-4-ethyl ester requires careful attention to the environment, temperature, impurities, packaging, and labeling to ensure its safety and avoid accidents.