Chemical Formula | C20H16O3S |
Molecular Weight | 336.404 g/mol |
Appearance | Solid (predicted) |
Boiling Point | Estimated around 500 - 600 °C under normal pressure (predicted) |
Melting Point | Estimated around 150 - 180 °C (predicted) |
Solubility | Poorly soluble in water, soluble in organic solvents like chloroform, dichloromethane (predicted) |
Density | Estimated around 1.3 - 1.4 g/cm³ (predicted) |
Flash Point | Estimated around 250 - 300 °C (predicted) |
Vapor Pressure | Very low vapor pressure at room temperature (predicted) |
Logp | Estimated around 5 - 6 (predicted) |
What is the chemical structure of 6,7,8,9 -tetrahydrodibenzo [b, d] furan-2 -ylthiophene-2 -carboxylate?
I am looking at this question and am inquiring about the chemical structure of 6, 7, 8, 9 -tetrahydrodinaphthalene [b, d] -azine-2-yl-2-carboxylamide. The structure of this compound is quite complex, so let me tell you in detail.
The structure of tetrahydrodinaphthalene [b, d] -azine is formed by hydrogenation of the skeleton of dihydrodinaphthalene [b, d] -azine and adding hydrogen at a specific position. In this skeleton, naphthalene rings are fused to each other and connected to the azine ring. The azine ring has one oxygen and one nitrogen atom, and its heterocyclic properties affect the chemical properties of the compound.
And the numbers 6, 7, 8, and 9 shall be the identification of the specific position of the tetrahydrodinaphthalene [b, d] -azine skeleton according to the organic chemistry nomenclature. As for the - 2 - group - 2 - carboxylamide part, the - 2 - group indicates a specific position to connect the substituent, which is a carboxylamide-containing structure. The carboxylamide is the - CONH 2 group, which is connected to the position numbered 2.
Overall, the chemical structure of 6, 7, 8, 9-tetrahydrodinaphthalene [b, d] -azine-2-yl-2-carboxylamide is based on tetrahydrodinaphthalene [b, d] -azine as the core skeleton, connected with carboxylamide substituents at specific positions, and the interaction of various parts endows this compound with unique chemical properties and reactivity. To accurately draw its structure, it is necessary to clearly display the atomic connection and spatial arrangement by lines and atomic symbols according to the rules of organic chemistry drawing.
What are the physical properties of 6,7,8,9 -tetrahydrodibenzo [b, d] furan-2 -ylthiophene-2 -carboxylate?
In "Tiangong Kaiwu", cyanodibenzo [b, d] azole has special properties. It is a second-degree carcinogen with formidable toxicity. It is occasionally involved in chemical industry, and its preparation is carried out with caution.
Cyanodibenzo [b, d] azole has the following physical properties: Under normal temperature, it is mostly in a crystalline state, with a white or yellowish color. The melting point is quite fixed, about [specific melting point value], which is an important feature. The boiling point also has a fixed number, about [specific boiling point value]. It is insoluble in water, but easily soluble in many types of organic solvents, such as ethanol and ether, due to the interaction between the molecular structure and the solvent. < Br >
In addition, its stability is also one. Under normal temperature, normal pressure and no special chemical action, the structure can be stable. In case of high temperature, open flame or strong oxidizing agent, it is easy to react and produce harmful substances. Therefore, when storing and using, it is necessary to be cautious, fire-proof and explosion-proof, in accordance with regulations, to ensure safety and security.
What are the chemical properties of 6,7,8,9 -tetrahydrodibenzo [b, d] furan-2 -ylthiophene-2 -carboxylate?
"Tiangong Kaiwu" says: heptanoic acid dialkali, sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, carbonic acid, boric acid, silicic acid, caustic soda and soda ash are also. However, the heptanoic acid dialkali mentioned in the title has different properties.
Sulfuric acid has strong corrosiveness, strong oxidation and water absorption. It can react with many metals, metal oxides and alkalis, and is widely used in industry, such as the preparation of fertilizers, pesticides, explosives, etc.
Hydrochloric acid is also corrosive and is a volatile strong acid. It is often seen in the fields of metal surface rust removal, pharmaceuticals, food processing, etc., and can react with metals, alkalis, and some salts.
Nitric acid is a strong oxidizing acid, highly corrosive, and often does not generate hydrogen when reacting with metals. It is mostly used in chemical, metallurgical and other industries to produce nitrates and nitro compounds.
Phosphoric acid is a medium-strong acid with certain corrosiveness. It plays a significant role in food additives, fertilizer manufacturing, water treatment, etc. It can participate in a variety of acid-base reactions and complexation reactions.
Carbonic acid is unstable and easily decomposes into carbon dioxide and water. It is commonly found in carbonated beverages. Its acidity is weak and it is of great significance in the natural carbon cycle.
Boric acid is weakly acidic and has the effect of disinfection and anti-corrosion. It is used in glass, ceramics, medicine and other industries and can be esterified with alcohols.
Silicic acid is a poorly soluble weak acid, mostly in the form of silicate, and is widely used in building materials, ceramics, glass and other industries.
Caustic soda, that is, sodium hydroxide, is highly corrosive, highly soluble in water and exothermic. It is a strong alkali, which can react with acids, acidic oxides, and certain salts. It is indispensable in papermaking, textiles, soap manufacturing and other industries.
Soda ash, that is, sodium carbonate, although it contains alkali in its name, it is actually a salt, and its aqueous solution is alkaline. It is widely used in glass manufacturing, chemical industry, food processing and other fields. It can react with acids and also undergo metathesis reactions with certain salts. < Br >
This heptanoic acid dibase plays an important role in many aspects such as chemical industry, industry, and life, and each plays a different role due to its unique chemical properties.
In what fields is 6,7,8,9 -tetrahydrodibenzo [b, d] furan-2 -ylthiophene-2 -carboxylate used?
"Tiangong Kaiwu" says: Seven-leaf gallbladder, that is, Gynostemma blue, is used in all fields.
It is in the field of medicine and has long been valued by physicians. According to reports, Gynostemma blue has many effects. Ancient healers, looking at its calmness, taste sweet and bitter, often used it as medicine. It can nourish qi and strengthen the spleen. For those with spleen deficiency syndrome, it can help the spleen to transport and transform, so that the middle qi is healthy and prosperous. And it has the ability to reduce phlegm and relieve cough. If you have a cough with a lot of phlegm, you can use Gynostema blue to treat it, which is very effective. It can also clear away heat and detoxify. For those with heat and poison in the body, it can relieve its poison and dissipate carbuncle and sores.
In the world of health, G In the past, people often picked its young leaves and made them into tea. Drinking it can refresh the mind and refresh the mind, making people refreshed, and working during the day without drowsiness. And long-term drinking seems to have the effect of prolonging life, so it is favored by health practitioners.
In the field of tea drinking, Gangchu blue tea has a unique flavor. The color of the tea soup is yellow-green and bright, the aroma is quiet, the taste is mellow in the mouth, and the sweetness lasts for a long time. Drinking this tea often can not only enjoy the fun of tea drinking, but also benefit physical and mental health.
It can be seen that Gangchu blue has its unique use in medicine, health care, tea drinking and other fields, and is really a treasure of nature.
What is the synthesis method of 6,7,8,9 -tetrahydrodibenzo [b, d] furan-2 -ylthiophene-2 -carboxylate?
The book "Tiangong Kaiwu" says: "Anyone who makes this thing needs to follow the ancient method and do it in sequence." To obtain 6% 2C7% 2C8% 2C9 -tetrahydrodinaphthalene [b, d] furan, the first thing to do is to clarify its physical properties and reaction reasons.
The synthesis of this compound can first use suitable starting materials, such as those with corresponding aromatic ring structures, through ingenious reaction design. Or a specific substituent can be introduced first to lay the foundation for the subsequent cyclization reaction.
If you want to make it, you can start with a compound with a similar structure, and under suitable reaction conditions, through a condensation reaction, the molecular skeleton can be initially built. For example, a raw material with an active aryl group is selected, and under the catalysis of a base, it reacts with a reagent containing an appropriate functional group to form a key carbon-carbon bond or a carbon-hetero bond.
Then, through the cyclization step, the molecule forms the target naphthalene-furan structure. This step requires precise regulation of reaction conditions, such as temperature, solvent, catalyst, etc. For example, under the catalysis of acid or Lewis acid, a ring-closing reaction within the molecule is induced to construct the desired fused ring system.
During the reaction process, close attention should be paid to the occurrence of side reactions, and the purity and yield of the product should be improved by optimizing reaction parameters, such as adjusting the ratio of reactants and reaction time. The pure 6% 2C7% 2C8% 2C9 -tetrahydrodinaphthalene [b, d] furan can be obtained by multi-step careful reaction operation and separation and purification. The synthesis road needs to be rigorous and meticulous, and according to the laws of chemistry, good results can be obtained.