1 Tert Butyl 2 Methyl 2 5 Dihydro 1h Pyrrole 1 2 Dicarboxylate
pyridine pyrrole pyrazine piperidine piperazine

1-tert-Butyl 2-methyl 2,5-dihydro-1H-pyrrole-1,2-dicarboxylate

    Specifications

    HS Code

    833941

    Chemical Formula C12H19NO4
    Molar Mass 241.28 g/mol
    Physical State Solid (assumed)
    Solubility Soluble in organic solvents like dichloromethane, chloroform
    Stability Stable under normal conditions, but may react with strong oxidizing agents
    Reactivity Can participate in reactions typical of pyrrole derivatives, such as electrophilic aromatic substitution

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    Where to Buy 1-tert-Butyl 2-methyl 2,5-dihydro-1H-pyrrole-1,2-dicarboxylate in China?
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    Frequently Asked Questions

    As a leading 1-tert-Butyl 2-methyl 2,5-dihydro-1H-pyrrole-1,2-dicarboxylate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the main use of 1-tert-Butyl 2-methyl 5-dihydro-1H-pyrrole-1, 2-dicarboxylate
    1-tert-butyl-2-methyl-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate is widely used in the field of organic synthesis.
    Its primary use lies in the key building blocks of heterocyclic compounds. The cover heterocyclic structure is widely found in many natural products, drugs and bioactive molecules. This compound contains the specific structure of pyrrole rings, which can be chemically modified to derive a variety of heterocyclic systems. For example, by reacting with different nucleophiles or electrophilic reagents, pyrrole rings can be functionalized with check point specificity, thereby creating novel and functionally specific heterocyclic compounds, which are of great significance in the development of new drugs.
    Furthermore, in the field of asymmetric synthesis, it also has important uses. Due to its chiral center or potential chiral induction ability, it can be used as a chiral auxiliary agent or a chiral source to induce the reaction to proceed in a specific stereochemical direction. By ingeniously designing reaction conditions and substrates, the use of this compound can efficiently prepare compounds with high optical purity, which is crucial in the fields of chiral drug synthesis and total synthesis of natural products, and can improve the biological activity and selectivity of the products.
    And in the field of materials science, with appropriate modification and polymerization, this compound may be able to construct polymer materials with special properties. The pyrrole ring structure endows the material with unique electronic properties and optical properties, which can be used to prepare optoelectronic materials, sensor materials, etc., opening up new avenues for the development of materials science.
    In summary, 1-tert-butyl-2-methyl-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate is a valuable compound in many fields such as organic synthesis, asymmetric synthesis and materials science, and plays a significant role in promoting the progress of related fields.
    What are the physical properties of 1-tert-Butyl 2-methyl 5-dihydro-1H-pyrrole-1, 2-dicarboxylate
    1-tert-butyl-2-methyl-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate, this compound is an organic compound with unique physical properties.
    Looking at its form, it is either liquid or solid at room temperature, but the exact state often depends on the intermolecular force and the surrounding ambient temperature. If the intermolecular attractive force is strong and the ambient temperature does not reach the melting point, it is solid, hard or brittle; if the intermolecular force is moderate and the temperature is higher than the melting point, it is liquid and flows smoothly.
    As for the color, if there is no conjugated system or chromogenic group, it is mostly colorless. If the structure contains a specific conjugated system, it may develop color. The higher the degree of conjugation, the darker the color.
    When it comes to odor, because it contains groups such as ester groups, or emits a unique aromatic smell, the exact smell of your mileage may vary, and it is also related to molecular volatility.
    In terms of solubility, according to the principle of "similar miscibility", it is an organic ester, which has good solubility in organic solvents such as ethanol, ether, and dichloromethane. Because these solvents are similar in structure to the compound, intermolecular forces can interact to promote its dissolution. However, the solubility in water is poor. Because water is a polar solvent, it is very different from the structure of the organic substance, and the intermolecular forces are difficult to match, so it is not easily soluble.
    The boiling point is as important as the melting point. The boiling point is affected by the intermolecular force and the relative molecular mass. If the relative molecular mass is large and the intermolecular force is strong, the boiling point will be higher, and more energy will be required to overcome the attractive force between molecules and make it gaseous. The melting point is related to the regularity of molecular arrangement. If the molecular arrangement is orderly and the lattice energy is large, the melting point will be high.
    Density is also a key property, which is related to the molecular mass and the degree of molecular packing. If the molecular mass is large and the packing is close, the density will be large; otherwise, it will be small. The density of this compound may be similar to that of common organic solvents.
    What is the chemical synthesis method of 1-tert-Butyl 2-methyl 5-dihydro-1H-pyrrole-1, 2-dicarboxylate
    To prepare 1-tert-butyl-2-methyl-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate, the following method can be followed.
    First, use suitable starting materials, such as pyrrole derivatives with specific substituents or related precursors. The alkenes containing suitable substituents can be added to compounds containing carboxyl groups or their activated forms. In this process, choose a reaction path with mild conditions and good yields.
    Or use the strategy of Diels-Alder reaction. Find a substance with a conjugated diene structure and an appropriate substituent group and a dienophilic body. The dienophilic body needs to contain a group that can be subsequently converted into a carboxyl ester group. During the reaction, control the temperature, solvent and other conditions to make the reaction proceed in the direction of generating the target product.
    After the preliminary product is formed, suitable esterification methods are used for the part of the product that needs to be converted into the target tert-butyl ester and methyl ester. For the formation of tert-butyl ester, tert-butyl alcohol can be used to react with the corresponding carboxyl group under acid catalysis or condensation agent. The methyl ester part can be esterified by reflux with methanol and carboxyl group using sulfuric acid as catalyst.
    After each step of the reaction, suitable separation and purification methods, such as column chromatography, recrystallization, etc., are required to obtain high-purity intermediate and final products to ensure the successful preparation of 1-tert-butyl-2-methyl-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate.
    1-Tert-Butyl 2-methyl 5-dihydro-1H-pyrrole-1, 2-dicarboxylate What are the precautions in storage and transportation?
    1-tert-butyl-2-methyl-2,5-dihydro-1H-pyrrole-1,2-dicarboxylic acid esters are organic compounds. When storing and transporting, many key matters should be paid attention to.
    First stability and reactivity. This compound contains pyrrole ring and carboxyl ester structure, which is active in nature and sensitive to light, heat and humidity. Store in a cool, dry and dark place away from fire and heat sources to prevent decomposition or reaction caused by excessive temperature. Due to its structural characteristics, or intense reaction with oxidants, reducing agents, acids, bases, etc., it cannot be mixed with various substances. < Br >
    Times and packaging. Packaging must be tight to prevent leakage. Commonly used glass, plastic or metal containers are packed, but the material should be selected according to its chemical properties. In case of active compounds, the glass container may need special treatment to prevent reaction with glass components; plastic packaging should be selected with good chemical stability to avoid corrosion. The name, nature, danger warning and other information of the compound must be clearly marked on the outside of the package.
    The second is transportation. Temperature control, vibration reduction and leakage prevention are required during transportation. When it is hot in summer, it may need to be refrigerated for transportation; when the road is bumpy, vibration reduction measures should be taken to prevent package damage. Transportation vehicles should also meet the standards for dangerous goods transportation, and be equipped with corresponding emergency treatment equipment and protective equipment.
    Finally, personnel protection. Those who come into contact with this compound should take necessary protective measures, such as protective clothing, protective gloves and goggles, operating in a well-ventilated place, or wearing a gas mask to prevent inhalation and contact damage to the body.
    In short, the storage and transportation of 1-tert-butyl-2-methyl-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate must be strictly controlled in terms of environment, packaging, transportation conditions, and personnel protection according to its chemical properties to ensure safety.
    What is the market price of 1-tert-Butyl 2-methyl 5-dihydro-1H-pyrrole-1, 2-dicarboxylate
    1-tert-butyl-2-methyl-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate, this is an organic compound. However, its market price is difficult to determine. The price is influenced by many factors, such as the difficulty of preparation, the cost of raw materials, the supply and demand situation of the market, and the scale of production.
    If the preparation of this compound requires rare or expensive raw materials, and the synthesis steps are difficult and the process requirements are strict, the production cost will be high, and the market price will also rise. On the contrary, if the raw materials are easy to obtain, the preparation process is simple, and the price will be relatively low.
    The situation of market supply and demand is also the key to affecting the price. If the market demand for this compound is strong and the supply is scarce, the price tends to rise; if the market demand is weak and the supply is sufficient, the price may decline.
    Furthermore, the size of the production scale also has an impact. In large-scale production, due to the scale effect, the unit production cost may be reduced, thus affecting the market price.
    As for the exact market price, it is necessary to check the chemical product trading platform in detail and inquire from the relevant chemical raw material suppliers to obtain an accurate number. The price of chemical products fluctuates frequently, and the prices of different suppliers, different purity and packaging specifications vary. Therefore, in order to know its exact price, it is necessary to inquire in real time and compare it carefully.