methyl propan-2-yl 4-(2,1,3-benzoxadiazol-4-yl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

"Methyl + propan - 2 - yl + 4- (2,1,3 - benzoxadiazol - 4 - yl) -2,6 - dimethyl - 1,4 - dihydropyridine - 3,5 - dicarboxylate" is the name of an organic compound. To clarify its chemical structure, it is necessary to analyze it according to the naming rules of organic chemistry.
"methyl", methyl is also an alkyl group containing one carbon. "Propan - 2 - yl", isopropyl is also, its structure is one carbon atom connected to the second carbon of propane, and another dimethyl. " 4 - (2,1,3 - benzoxadiazol - 4 - yl) ", showing that benzo [2,1,3] oxadiazol - 4 - is connected to the fourth position of the main structure. This benzoxadiazole structure is formed by fusing a benzene ring with an oxadiazole ring.
" 2,6 - dimethyl - 1,4 - dihydropyridine - 3,5 - dicarboxylate ", the main structure is 1,4 - dihydropyridine ring, the ring positions 2 and 6 are each connected to a methyl group, and positions 3 and 5 are dicarboxylate groups. Where" dicarboxylate "is also a carboxylate group.
In summary, the structure of this compound is composed of a 1,4-dihydropyridine ring as the core, with methyl groups at the 2nd and 6th positions, carboxylic acid ester groups at the 3rd and 5th positions, methyl and isopropyl carboxylic acid esters, respectively, and benzo [2,1,3] oxadiazole-4-group at the 4th position. Its complex and delicate structure may be of great significance in the fields of organic synthesis and pharmaceutical chemistry, because of its unique structure or specific chemical and biological activities.

Methyl-isopropyl-4- (2,1,3-benzoxadiazole-4-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate, which has a wide range of uses. In the field of medicine, it can be used as a pharmaceutical active ingredient. With its unique chemical structure, it can be combined with specific targets in organisms to play a role in regulating physiological functions, such as participating in cell signaling pathways, affecting cell metabolism and proliferation, and may have potential value in the treatment of certain diseases. In the field of materials science, it may be used to prepare materials with special properties. Due to its structural properties, it may endow materials with unique properties such as optics and electricity, such as in photovoltaic materials, or it can optimize the light absorption and emission properties of materials for the manufacture of photovoltaic devices such as Light Emitting Diodes and solar cells. In the field of organic synthesis, it may also be a key intermediate. With its various active functional groups, it can build more complex organic compounds through various organic reactions, providing an important material foundation for the development of organic synthetic chemistry, and helping to synthesize new drugs, materials and other functional compounds, promoting the continuous development of chemical science.

"Methyl + propan - 2 - yl + 4- (2,1,3 - benzoxadiazol - 4 - yl) - 2,6 - dimethyl - 1,4 - dihydropyridine - 3,5 - dicarboxylate" is the English name of an organic compound. Its physical properties can probably be inferred from the following numbers.
First, the properties of such 1,4 - dihydropyridine derivatives containing polycyclic and heterocyclic rings are often solid, mostly crystalline, and the cover is arranged in an orderly manner due to intermolecular forces, such as van der Waals forces and hydrogen bonds.
In addition to the melting point, in the molecular structure, benzooxadiazole ring, dihydropyridine ring and ester group interact to make the molecules bond tightly. Therefore, its melting point may be higher, and it is estimated that it is above 100 ° C. Due to the increase of molecular rigidity in the benzene ring and heterocyclic system, and the weak interaction between ester groups can be formed, the melting point is increased.
In terms of solubility, this compound contains polar groups such as ester groups and has a large non-polar aromatic ring structure. Therefore, in polar organic solvents, such as ethanol and acetone, there may be a certain solubility. Because polar groups can form hydrogen bonds or dipole-dipole interactions with polar solvent molecules. However, in water, the solubility may be limited, and the non-polar aromatic ring partially hinders its affinity with water, and the hydrogen bond network of water cannot tolerate this macromolecule.
As for the density, because the molecule contains benzene rings, heterocycles and multiple hydrocarbon groups, the structure is compact and the relative molecular weight is large. Therefore, its density may be greater than that of water, between 1.2 and 1.4 g/cm ³, which is slightly heavier than that of water.
The physical properties of this compound are determined by its unique molecular structure, in which the groups interact and co-shape its properties.

The synthesis of methyl-isopropyl-4- (2,1,3-benzoxadiazole-4-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid esters is a key area of inquiry in organic synthetic chemistry. The synthesis process often follows a multi-step reaction path, and has undergone ingenious design and precise operation.
The first step often requires the preparation of specific starting materials, such as compounds containing benzoxadiazole structures, which form the core skeleton of the target molecule. Or through the electrophilic substitution reaction of aromatics, a specific functional group can be introduced into the benzene ring, and then through the cyclization reaction, the ring structure of benzoxadiazole can be precisely constructed.
The second step is related to the construction of the pyridine ring. The formation of the 1,4-dihydropyridine ring is achieved by the condensation reaction, such as the Hantzsch reaction, using suitable alcaldes, ketones and nitrogen-containing compounds as raw materials. In this process, careful regulation of reaction conditions, such as temperature, solvent and catalyst dosage, is crucial because it can significantly affect the selectivity and yield of the reaction.
Furthermore, for the introduction of dimethyl substituents, or appropriate alkylating reagents can be selected to achieve the substitution of methyl groups at specific positions in the pyridine ring. This step requires careful consideration of the activity of the reaction check point to ensure that the substituents fall precisely at the 2,6-position.
As for the introduction of ester groups, the esterification reaction of carboxylic acids and alcohols under the action of catalysts can be achieved. Methyl ester groups and isopropyl ester groups are introduced by selecting methyl alcohol and isopropyl alcohol, respectively. The entire synthesis process requires the use of modern analytical techniques, such as nuclear magnetic resonance (NMR), mass spectrometry (MS), and infrared spectroscopy (IR), to accurately monitor the reaction process, identify the structure of the intermediate product and the target product, and ensure that the synthesis path is correct. Ultimately, this complex organic compound is efficiently obtained.

Methyl-2-isopropyl-4- (2,1,3-benzoxadiazole-4-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate This compound is related to safety and is a matter of great importance.
Looking at its properties, this compound is an organic molecule obtained by chemical synthesis. Its structure is complex and contains specific structural fragments such as benzoxadiazole and dihydropyridine. The unique structure is often closely related to its properties. It can be deduced from its structure, or it has a certain stability, but it also needs to be studied carefully. < Br >
When it comes to toxicity, when relevant experimental data are lacking, it should not be rashly concluded that it is non-toxic. Many chemicals with similar complex structures, or due to specific groups, have potential toxicity. For example, some nitrogen-containing heterocyclic structures may cause adverse reactions in organisms and interfere with physiological processes.
The chemical stability of
is repeated. Although it contains a dihydropyridine structure and has a certain conjugate system, it has a certain tendency to stabilize. In case of extreme conditions such as strong acids, strong bases or high temperatures, it may react, cause structural changes, or produce harmful by-products.
And its behavior in the environment also needs to be considered. If accidentally released in the environment, due to complex structure, or difficult to be rapidly degraded by natural microorganisms, it will accumulate and affect the ecology. Its potential impact on aquatic and soil organisms should not be underestimated.
Therefore, this methyl-2-isopropyl-4- (2,1,3-benzoxadiazole-4-yl) -2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate, although the exact safety characteristics are not known, but based on the experience of chemical structure and analogs, it needs to be treated with caution. After comprehensive and in-depth research, its safety profile can be clarified.