Isopropyl Methyl 4 4 Benzofurazanyl 1 4 Dihydro 2 6 Dimethyl 3 5 Pyridinedicarboxylate
pyridine pyrrole pyrazine piperidine piperazine

Isopropyl methyl (+-)-4-(4-benzofurazanyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate

    Specifications

    HS Code

    436846

    Chemical Formula C20H22N2O6
    Molecular Weight 386.40
    Appearance Typically a solid (state may vary depending on purity and conditions)
    Solubility Solubility characteristics would depend on the solvent, likely sparingly soluble in water but more soluble in organic solvents like ethanol, dichloromethane etc.
    Melting Point Data would be required from experimental determination
    Boiling Point Estimation would be needed based on related compounds, as direct data may be scarce
    Density Requires experimental measurement for accurate value
    Pka Dependent on the acidic/basic groups in the molecule, data from titration experiments needed
    Logp Indicates lipophilicity, value can be estimated or measured experimentally
    Vapor Pressure Would be low as it is likely a solid, experimental determination needed for exact value

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    Frequently Asked Questions

    As a leading Isopropyl methyl (+-)-4-(4-benzofurazanyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate 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 chemical structure of Isopropyl methyl (+ -) -4- (4-benzofurazanyl) -1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
    The chemical structure of isopropylmethyl (±) -4- (4-benzofuryl) -1,4-dihydro-2,6-dimethyl-3,5-pyridine dicarboxylate is as follows:
    The core structure of this compound is a pyridine ring, with a specific substituent at the 1,4-dihydro position of the pyridine ring. The 2,6-positions of the pyridine ring are connected to methyl groups, respectively, which endow the pyridine ring with specific steric resistance and electronic effects. The 3,5-position is connected to the diformate structure, that is, one carboxyl group is esterified to form isopropyl ester, and the other carboxyl group is esterified to form methyl ester. The presence of this ester group not only affects the polarity of the molecule, but also may play a role in chemical reactions and biological activities.
    And in the 4-position of the pyridine ring is connected to the 4-benzofuran group, which acts as a fused ring aromatic system and adds a conjugated structure to the whole molecule, thereby affecting the electron cloud distribution, stability and spectral properties of the molecule. Due to the existence of (±) -labeling, it is suggested that the compound may have a chiral center and a pair of enantiomers, which may have an important impact on biological activity and chemical reaction selectivity. Overall, the structure of the compound is relatively complex, and the interaction between each substituent determines its physicochemical properties and potential biological activities.
    What are the physical properties of Isopropyl methyl (+ -) -4- (4-benzofurazanyl) -1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
    Isopropylmethyl (±) -4- (4-benzofuranyl) -1,4-dihydro-2,6-dimethyl-3,5-pyridyl dicarboxylate, the properties of this substance are quite specific, and there are many things that can be described about its physical properties.
    On the surface, it is mostly colorless to light yellow crystalline powder, just like finely crushed agarwood, delicate and uniform. Looking at it, it has a certain luster, like a faint light looming in it, shining brightly.
    When it comes to melting point, it is usually maintained within a specific range, which is one of the important characteristics to determine its purity. The exact value of its melting point, like a scale on a precision balance, accurately delineates the critical transition of a substance from a solid state to a liquid state.
    Solubility is also a key physical property. In common organic solvents, such as ethanol and chloroform, it exhibits good solubility, just like the water of a fish, which can dissolve with solvents to form a uniform solution. In water, its solubility is relatively limited, just like oil floating in water, it is distinct and difficult to blend.
    In addition, density is also one of its physical properties. The value of this density, just like the "weight code" of a substance, determines its ups and downs in different media, and also plays a subtle role when interacting with other substances.
    Its stability is relatively impressive under normal conditions, but if it encounters high temperature, strong light or specific chemical reagents, it will also change, just like throwing stones into a quiet lake, causing layers of ripples, causing changes in molecular structure, which in turn affects its physical properties.
    In this way, the physical properties of isopropylmethyl (±) -4- (4-benzofuranyl) -1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid ester exhibit unique states in many aspects, laying the foundation for its application in various fields.
    Isopropyl methyl (+ -) -4- (4-benzofurazanyl) -1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate What is the application field?
    Isopropylmethyl (±) - 4 - (4 - benzofurazyl) - 1,4 - dihydro - 2,6 - dimethyl - 3,5 - pyridinedicarboxylate has a wide range of application fields.
    In the field of medicine, or may have potential medicinal value. Geyin pyridinedicarboxylate compounds are often biologically active or can participate in the regulation of human physiological processes. Benzofurazanyl in its structure may endow the compound with specific pharmacological properties, or it can be developed as a lead compound for drugs to treat specific diseases, such as inflammation, cardiovascular diseases and other related drugs. By modifying its structure and exploring the interaction with biological targets, it is expected to develop new drugs with high efficiency and low toxicity.
    In the field of materials science, such compounds may also have extraordinary performance. Such compounds may be made into materials with special properties by specific processes. Or because of the regularity and functionality of its molecular structure, they can be used to prepare optical materials, or have special responses to light, and are used in optoelectronic devices, such as Light Emitting Diode, photosensors, etc., which contribute to the development of the optoelectronics industry.
    In the field of agriculture, it may play a unique role. Pyridinedicarboxylic esters, some of which have certain biological activities, or have inhibitory or control effects on crop diseases and pests. Or can be developed as new pesticides, with high efficiency, low toxicity and environmental friendliness, which help the sustainable development of agriculture, reduce the harm of traditional pesticides to the environment, and ensure the quality and safety of agricultural products.
    Isopropyl methyl (+ -) -4- (4-benzofurazanyl) -1,4-dihydro-2,6-dimethyl-3,What are the synthesis methods of 5-pyridinedicarboxylate
    The synthesis method of isopropylmethyl (±) -4- (4-benzofurazyl) -1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate is an important research content in organic synthetic chemistry. The synthesis step is often based on benzofurazan compounds as the starting material, and the target product is obtained after several delicate reactions.
    At the beginning, take a specific structure of benzofurazan, add an appropriate amount of catalyst and solvent in a suitable reaction vessel to initiate the reaction. The choice of this catalyst is crucial, and it needs to be carefully selected according to the reaction mechanism and substrate characteristics in order to promote the efficient progress of the reaction. Common catalysts include metal salts or organic bases, which can effectively catalyze the formation and cleavage of chemical bonds between substrate molecules.
    Then, the raw material containing pyridine structure is added to condensate with benzofurazan derivatives. This process requires precise control of the reaction temperature and time. If the temperature is too high or too low, and the time is too long or too short, it may affect the reaction yield and product purity. The reaction temperature may be maintained at a specific range, such as 60 to 80 degrees Celsius, to ensure a smooth and orderly progress of the reaction.
    Subsequently, the reaction intermediate is modified to introduce isopropyl and methyl groups. This step is often achieved by alkylation reaction. Appropriate alkylation reagents are selected. Under the action of alkali, the specific position of the intermediate is alkylated, so as to construct the specific structure of the target product.
    After the reaction is completed, the product needs to be separated and purified. Commonly used methods include column chromatography, recrystallization, etc. Column chromatography can use the difference in the distribution coefficient of different compounds between the stationary phase and the mobile phase to achieve effective separation of products and impurities. The recrystallization method can obtain high-purity target products through multiple crystallization operations according to the different solubility of the product and impurities in a specific solvent with temperature changes.
    Synthesis of isopropylmethyl (±) -4- (4-benzofurazyl) -1,4-dihydro-2,6-dimethyl-3,5-pyridyldicarboxylate requires comprehensive consideration of raw material selection, reaction conditions control, and product purification. Each step is closely linked and complementary to each other in order to successfully prepare this compound.
    What is the market outlook for Isopropyl methyl (+ -) -4- (4-benzofurazanyl) -1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate?
    Nowadays, it is called isopropylmethyl (±) -4- (4-benzofurazyl) -1,4-dihydro-2,6-dimethyl-3,5-pyridyldicarboxylate. The market prospect of this product is related to many aspects.
    According to its properties, this compound has a unique chemical structure, or a combination of benzofurazyl and pyridyldicarboxylate groups, showing different physical and chemical properties, or potential application value in specific fields. However, its market prospect depends on the wide range of applications.
    In the field of medicine, if it can demonstrate pharmacological activity, such as anti-inflammatory, anti-tumor, etc., and its safety and effectiveness have been demonstrated by rigorous experiments, it will definitely attract the attention of pharmaceutical companies and enter the R & D process. The prospect is promising. However, pharmaceutical research and development takes a long time, requires huge investment, and has many barriers. It is difficult to become a drug on the market.
    In the field of materials, if it can improve material properties, such as enhancing material stability and endowing special optical and electrical properties, it can also find a market. For example, in the synthesis of new polymer materials, it is used as an additive or structural unit to improve material quality. However, the competition in the new material market is fierce, and it must compete with existing materials. It needs to have outstanding advantages in order to gain market recognition.
    Furthermore, the difficulty of the preparation process also affects the market prospect. If the preparation process is cumbersome and costly, even if the performance is superior, the promotion is limited. It is necessary to find efficient and economical preparation methods to reduce costs in order to expand market share.
    At present, although there are potential opportunities due to the unique structure, if you want to open up the market, you still need to make efforts in application research, process optimization and other aspects to break through many obstacles. Only then can you hope to occupy a place in the market. The prospects are good and bad, and it is difficult to judge. It all depends on the follow-up research and development.