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What is the chemical structure of 2- (4-iodophenyl) -3- (4-nitrophenyl) -5-phenyl-2, 3-dihydro-1h-tetrazole Hydrochloride (1:1)
This is an organic compound named 2- (4-iodophenyl) -3- (4-nitrophenyl) -5-phenyl-2,3-dihydro-1H-tetrazolium hydrochloride (1:1). Looking at its name, this compound has a complex structure and is composed of many parts.
First look at the main body, which is the structure of 2,3-dihydro-1H-tetrazolium. In the second position of the main structure, there is (4-iodophenyl), which is a group containing an iodine atom and the iodine is located in the fourth position of the benzene ring. The 3-position is connected to (4-nitrophenyl), which means that the 4-position of the benzene ring has a nitro group. The 5-position is connected to a phenyl group. And because of the suffix of hydrochloride (1:1), it can be seen that this compound forms a salt of hydrochloric acid in a ratio of 1:1, that is, in the structure of the compound, each main structural unit corresponds to a molecule of hydrochloric acid.
In this way, the chemical structure of 2- (4-iodophenyl) -3- (4-nitrophenyl) -5-phenyl-2,3-dihydro-1H-tetrazolium hydrochloride (1:1) is outlined.
What are the physical properties of 2- (4-iodophenyl) -3- (4-nitrophenyl) -5-phenyl-2, 3-dihydro-1h-tetrazole Hydrochloride (1:1)
2-% 284-iodophenyl% 29-3-% 284-nitrophenyl% 29-5-phenyl-2% 2C3-dihydro-1H-tetrazolium hydrochloride (1:1), this is an organic compound. Its physical properties are quite critical, let me tell them one by one.
Looking at its morphology, it may be in the state of crystalline powder at room temperature and pressure, and its color may be off-white to light yellow. The melting point of this compound has been investigated by many experiments, or within a certain range, but the exact value still needs to be determined according to the specific experimental conditions. The determination of the melting point is crucial to identify its purity and characteristics.
Solubility is also an important physical property. In organic solvents, their solubility may vary. In polar organic solvents, such as methanol and ethanol, there may be a certain solubility, because some groups in the molecular structure can interact with polar solvents. However, in non-polar organic solvents, such as n-hexane, toluene, etc., the solubility may be low, due to the mismatch between molecular polarity and non-polar solvents.
In addition, its stability also needs to be considered. Under conventional environmental conditions, if there are no special factors, its structure may be relatively stable. However, under extreme conditions such as high temperature, strong light, strong acid and alkali, or chemical changes occur, resulting in structural changes. The physical properties of this compound are of great significance in organic synthesis, drug development and other fields, and can provide important basis for related research and applications.
What is the use of 2- (4-iodophenyl) -3- (4-nitrophenyl) -5-phenyl-2, 3-dihydro-1h-tetrazole Hydrochloride (1:1)
2-% 284-iodophenyl% 29-3-% 284-nitrophenyl% 29-5-phenyl-2% 2C3-dihydro-1H-tetrazolium hydrochloride (1:1), this is a special chemical substance. Its uses are quite extensive and have been demonstrated in many fields.
In the field of scientific research, it can be used as a key intermediate in organic synthesis. Through specific chemical reactions, it can be skillfully converted into other complex and unique organic compounds. Due to the unique structure of this compound, it contains special functional groups such as iodine, nitro and phenyl. These functional groups endow it with special chemical activities and reaction characteristics, which can open up novel paths for organic synthesis and help scientists prepare compounds with specific functions, such as biological activities, optical properties or electrical properties, thereby promoting the in-depth development of organic chemistry.
In the field of drug research and development, it also has important uses. Due to its structural properties, it may have potential biological activities. Researchers can conduct in-depth studies on it to explore its interaction with specific targets in organisms. If its mechanism of action and targets can be accurately discovered, it may be developed into new drugs for the treatment of specific diseases. For example, some compounds containing similar structures have been shown to inhibit the growth of specific cancer cells, so the substance may also make its mark in the field of anti-cancer drug development.
In the field of materials science, it also has potential application value. By virtue of the characteristics of the groups in its structure, it may be used to prepare materials with special properties. For example, by using it to combine with other materials, the composite material is endowed with unique optical, electrical or mechanical properties, which contributes to the innovative development of materials science.
What is the synthesis method of 2- (4-iodophenyl) -3- (4-nitrophenyl) -5-phenyl-2, 3-dihydro-1h-tetrazole Hydrochloride (1:1)
To prepare 2 - (4 - iodophenyl) -3 - (4 - nitrophenyl) -5 - phenyl - 2,3 - dihydro - 1H - tetrazolium hydrochloride (1:1), the synthesis method is as follows.
First of all, it is necessary to use suitable starting materials, often take iodine-containing benzene derivatives, nitro-containing benzene derivatives and phenyl-containing reagents. First, the iodine-containing benzene derivatives react with specific reagents to construct a preliminary skeleton structure. This step may need to be carried out in a suitable solvent, such as dichloromethane, N, N-dimethylformamide, etc., and may need to add alkali substances to promote the reaction, such as potassium carbonate, triethylamine, etc. The reaction temperature also needs to be precisely controlled, or it depends on the specific reaction conditions between room temperature and heating reflux.
Then combine this intermediate product with a nitrobenzene-containing derivative. This process may involve reaction steps such as nucleophilic substitution and cyclization. During nucleophilic substitution, a reactant with suitable activity should be selected to ensure the smooth progress of the reaction. Cyclization requires specific reaction conditions or the addition of catalysts, such as some metal salt catalysts, to promote the formation of tetrazole structures in the molecule.
Finally, hydrochloric acid is introduced into the obtained product to form a salt, and the target product is 2 - (4 - iodophenyl) -3 - (4 - nitrophenyl) -5 - phenyl - 2,3 - dihydro - 1H - tetrazolium hydrochloride (1:1). During the salt formation process, the amount and addition speed of hydrochloric acid need to be controlled, and the pH of the reaction environment, temperature and other factors have an impact on the purity and yield of the product, so it should be carefully regulated. During the entire synthesis process, separation and purification operations, such as column chromatography and recrystallization, are required after each step of the reaction to ensure the purity of the intermediate and final products, thereby improving the synthesis efficiency and product quality.
What are the relevant safety precautions for 2- (4-iodophenyl) -3- (4-nitrophenyl) -5-phenyl-2, 3-dihydro-1h-tetrazole Hydrochloride (1:1)
2-% 284-Iodophenyl% 29-3-% 284-nitrophenyl% 29-5-phenyl-2% 2C3-dihydro-1H-tetrazolium hydrochloride (1:1), this is a rather special chemical substance. When using, many safety precautions must be kept in mind.
Bear the brunt, because of its chemical activity, it is very likely to cause damage to the human body when exposed. Contact with skin, or cause symptoms of allergy or irritation, if accidentally touched, immediately rinse with plenty of water and seek medical assistance as appropriate. The risk of eye exposure should not be underestimated. Once accidentally entered the eye, be sure to open the eyelids immediately, rinse thoroughly with flowing water or normal saline, and then seek medical attention quickly.
Furthermore, inhaling the dust or volatiles of this substance can be very harmful to the respiratory tract, or cause symptoms such as cough, asthma, and breathing difficulties. In the place of use, good ventilation is essential, and appropriate protective masks should be worn to block harmful substances from invading the respiratory tract.
Swallowing this substance is also dangerous, or causes gastrointestinal discomfort, such as nausea, vomiting, abdominal pain and other symptoms may occur. Once swallowed by mistake, do not induce vomiting on your own, you should seek medical attention immediately and follow your doctor's advice.
In addition, the chemical is also careful in storage. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources, and avoid mixing with oxidizing substances, acidic substances, etc., to prevent chemical reactions and cause danger.
During operation, all kinds of protective measures must be in place. In addition to the protective masks mentioned above, protective gloves, goggles, etc. need to be worn to ensure their own safety in an all-round way. After use, properly dispose of the remaining substances and waste, and must not be discarded at will to prevent pollution to the environment. In short, when dealing with this chemical substance, we should adopt a cautious attitude and strictly abide by relevant safety regulations to ensure personal safety and the environment are not damaged.
