Methyl 2 Methylpropyl 2 6 Dimethyl 4 2 Nitrophenyl 1 4 Dihydropyridine 3 5 Dicarboxylate
pyridine pyrrole pyrazine piperidine piperazine

methyl 2-methylpropyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate

    Specifications

    HS Code

    739099

    Chemical Formula C21H24N2O7
    Molar Mass 416.425 g/mol
    Physical State Solid (usually)
    Appearance Yellow - colored solid
    Melting Point Specific value would need experimental determination
    Boiling Point Decomposes before boiling
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Experimental value required
    Stability Stable under normal conditions, but sensitive to strong oxidizing agents
    Odor Odorless or very faint odor

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    Frequently Asked Questions

    As a leading methyl 2-methylpropyl 2,6-dimethyl-4-(2-nitrophenyl)-1,4-dihydropyridine-3,5-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 chemical structure of this product "methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate"?
    This is "methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate", and its chemical structure is a class of dihydropyridine derivatives. This compound contains a dihydropyridine core structure, with methyl at the 2,6 positions of the pyridine ring, 2 - nitrophenyl at the 4 position, and carboxyl at the 3,5 positions, respectively. It exists in the form of an ester group. The carboxyl group at the 2 position is connected to the methyl group, and the other carboxyl group is estered with 2 - methylpropyl. Such structures are of great significance in medicinal chemistry. Many calcium channel blockers have dihydropyridine structures, which interact with calcium channels to regulate intracellular and intracellular calcium ion flow and affect physiological processes such as cardiovascular. This compound may have similar pharmacological activities or be used as a lead compound for drug development for researchers to further explore its physiological activity and medicinal potential.
    What are the main uses of "methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate" products?
    "Methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate", this is a chemical substance, often called nifedipine-related derivatives. It has a wide range of uses and is a key raw material for the preparation of cardiovascular drugs in the field of medicine.
    Cardiovascular disease, like a hidden haze, threatens the health of the people. This compound is like a brave defender, and has shown extraordinary efficacy in the development of anti-hypertensive drugs. It can precisely act on vascular smooth muscles, dilate blood vessels, and widen the path for congested rivers, allowing blood to flow unimpeded, thereby effectively lowering blood pressure and protecting the well-being of patients.
    It also plays an important role in the development of drugs for the treatment of coronary heart disease. It can increase the blood flow of the coronary arteries, which is like attracting a clear spring to a dry place, providing sufficient nutrients for the myocardium, relieving the symptoms of myocardial ischemia, and rejuvenating the heart.
    In the field of organic synthesis, this substance is like a magical cornerstone, an important intermediate for the construction of complex organic molecules. With its unique chemical structure and reactivity, it can participate in many organic reactions, like the bricks and stones that build an exquisite pavilion, helping to synthesize a series of organic compounds with specific biological activities or functions, promoting the vigorous development of organic synthesis chemistry.
    What are the synthesis methods of "methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate" product?
    To prepare "methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate", there are many methods, and the following are common synthesis pathways.
    First, the classic Hantzsch reaction can be used. First take methyl acetoacetate, 2 - nitrobenzaldehyde and ammonia source (such as ammonium acetate), add a catalyst in an alcohol solvent, such as Lewis acid (such as ZnCl ²), heat and reflux. In this process, 2-nitrobenzaldehyde is condensed with methyl acetoacetate, and the ammonia source provides nitrogen atoms. After a multi-step reaction, a 1,4-dihydropyridine ring is constructed to obtain the target product. The advantage is that the reaction conditions are relatively mild, and the raw materials are common and easy to obtain; however, there are also deficiencies, side reactions or more, and the reaction conditions and separation and purification need to be carefully controlled.
    Second, the metal-catalyzed synthesis method. Use palladium, copper and other metal catalysts to select suitable ligands to catalyze the reaction of pyridine-containing ring precursors with halogenated hydrocarbons or other electrophilic reagents. If a suitable pyridine derivative is used as the substrate and coupled with halogenated esters under metal catalysis, the target molecule is synthesized through multi-step conversion. This method has the characteristics of high selectivity and good atomic economy, but the cost of metal catalysts is high, and the reaction conditions are required to be precise.
    Third, microwave-assisted synthesis method. The reactants are placed in a microwave reactor in proportion, with appropriate solvents and catalysts, and the rapid heating characteristics of microwaves are used to accelerate the reaction process. This method can greatly shorten the reaction time, improve the reaction efficiency, and promote some reactions that are difficult to occur under traditional conditions. However, specific microwave equipment is required, and the reaction system requirements are also stricter. < Br >
    When synthesizing "methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate", it is necessary to consider the raw material cost, equipment conditions, target product purity and other factors according to the actual situation, select the optimal synthesis method, and optimize it through multiple experiments before it can be successfully prepared.
    What is the market outlook for "methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate" products?
    "Methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate", this is the name of the chemical substance, and its market prospect is related to many aspects.
    Looking at the current medical field, cardiovascular diseases are quite common, and many cardiovascular drug research and development often involve compounds containing such structures. Gein 1,4 - dihydropyridine compounds have unique pharmacological activities and play an important role in regulating the function of the cardiovascular system. If this substance can show good antihypertensive, anti-angina and other effects, and has good safety and few side effects, it will definitely gain a place in the cardiovascular drug market and have a bright future.
    Furthermore, scientific research is also the key. Researchers are constantly looking for compounds with novel activities, which may arouse the interest of the scientific research community due to their unique chemical structure. If in-depth research reveals new biological activities or medicinal potential, it will open up new research and development directions, attract pharmaceutical companies to invest, and drive market demand growth.
    However, it also faces challenges. The complexity and cost of the chemical synthesis process affect its large-scale production and marketing activities. If the synthesis process is cumbersome and costly, it will be at a disadvantage in market competition. And the development of new drugs requires rigorous clinical trials to prove their safety and effectiveness. This process is long and costly, or it may become an obstacle to market advancement.
    Overall, if we can break through the bottleneck of the synthesis process and successfully pass the clinical trial, in the field of medicine and related scientific research, "methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate" has a considerable market prospect, but the challenges on the way should not be underestimated. After much research and efforts, we can open up a broad market space.
    "Methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate" What are the precautions during use?
    "Methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate" This substance is a chemical agent. When using it, be sure to pay attention to many matters.
    Bear the brunt, and safety protection must not be forgotten. Because it has certain chemical activity, or potential harm to the human body. During operation, you must wear professional protective equipment, such as protective clothing, protective gloves and protective goggles, to prevent the agent from contacting the skin and eyes. In case of accidental contact, rinse with plenty of water immediately, and seek medical treatment in time according to the specific situation.
    Furthermore, storage conditions are crucial. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Due to its chemical properties, high temperature, humid environment or deterioration can affect the use effect and even cause safety accidents. At the same time, it should be stored separately from oxidants, acids, alkalis and other chemicals to avoid chemical reactions caused by mixed storage.
    During use, strictly follow the established operating procedures. Precisely control the dosage and accurately weigh it according to actual needs and reaction requirements. Because it is an important intermediate in organic synthesis, improper dosage or unbalanced reaction will affect the quality and yield of the product. And the operation should be carried out in a fume hood to ensure that the generated harmful gases are discharged in time to ensure the health of the operator.
    In addition, after use, properly dispose of the remaining chemicals and waste. Do not dump at will, and should be treated harmlessly in accordance with relevant environmental protection regulations to prevent pollution to the environment. Used appliances should also be thoroughly cleaned to avoid residual agents affecting subsequent experiments or production.
    Only by paying careful attention to the above matters can the use of "methyl 2 - methylpropyl 2,6 - dimethyl - 4 - (2 - nitrophenyl) -1,4 - dihydropyridine - 3,5 - dicarboxylate" not only ensures safety, but also ensures the use effect and achieves the intended purpose.