(3Z)-5-[(4,6-Dichloro-1,3,5-Triazin-2-Yl)Amino]-4-Oxo-3-(Phenylhydrazono)-3,4-Dihydronaphthalene-2,7-Disulfonic Acid

This substance is (3Z) -5- [ (4,6-dihydroxy-1,3,5-triazine-2-yl) amino] -4-oxo-3- (benzoyl) -3,4-dihydropyrimidine-2,7-dione. The following describes its relevance in the form of ancient classical Chinese:
There is a substance today, and its chemical identification is (3Z) -5- [ (4,6-dihydroxy-1,3,5-triazine-2-yl) amino] -4-oxo-3- (benzoyl) -3,4-dihydropyrimidine-2,7-dione. Looking at its structure, it contains a ring system of triazine and pyrimidine, and is connected with hydroxyl, amino, oxo, benzoyl and other groups. These groups interact with each other, giving them unique properties.
can be deduced from its structure, or has certain chemical activity. Hydroxyl groups can participate in the formation of hydrogen bonds, affecting their solubility and intermolecular interactions. Amino groups can also involve chemical reactions, such as nucleophilic substitution. Oxygen groups can show their oxidation state and play a key role in redox reactions. Benzoyl groups add their hydrophobicity, or affect their dispersion in different solvents.
Although its specific properties and uses are not mentioned, such structures may have potential value in organic synthesis, pharmaceutical chemistry, etc. Or can be used as pharmaceutical intermediates, because the structures of pyrimidine and triazine are common in many drugs, by which molecules with specific pharmacological activities can be prepared. Or in materials science, it can be used to prepare functional materials because of its special structure that can interact with other molecules.

(3Z) -5- [ (4,6-dioxo-1,3,5-triazine-2-yl) amino] -4-oxo-3- (benzyl) -3,4-dihydropyrimidine-2,7-diacid, this substance is acidic, and hydrogen ions can be ionized due to the carboxyl group. It has certain stability, and its structure is rich in heterocycles and double bonds.
It can undergo substitution reactions, such as amino groups and carboxyl groups can be replaced by other groups. Taking carboxyl groups as an example, it can esterify with alcohols catalyzed by acids to form corresponding esters.
can also carry out addition reactions. The double bond in the molecule can be added with electrophilic reagents, such as with hydrogen halide, according to the Markov rule, hydrogen is added to the double bond carbon containing more hydrogen.
Hydrolysis can also occur. If under basic conditions, ester bonds, amide bonds, etc. can be hydrolyzed to generate corresponding carboxylic acids, alcohols, amines and other products. In the field of organic synthesis, due to its unique chemical properties, it can be used as an intermediate to synthesize complex organic compounds.

(3Z) -5- [ (4,6-dioxy-1,3,5-triazine-2-yl) amino] -4-oxo-3- (benzoyl) -3,4-dihydroquinazoline-2,7-diacid, this compound has certain applications in the fields of medicinal chemistry and organic synthesis.
In the field of medicinal chemistry, such complex organic compounds are often studied as potential pharmaceutical active ingredients. Its unique molecular structure gives it the possibility to interact with specific biological targets, such as enzymes or receptors that may bind to certain diseases, thereby regulating physiological processes in organisms and achieving the purpose of treating diseases, such as for the development of innovative drugs for specific cancers, inflammation and other diseases.
In the field of organic synthesis, it is an important synthetic intermediate. Organic chemists can introduce different functional groups by modifying and derivatizing its structure, thereby constructing more organic compounds with unique properties and functions, enriching the library of organic compounds, and providing diverse raw materials for further drug development, materials science and other research. In this way, this compound plays an important role in several key fields, promoting the development of related scientific research and technological applications.

The synthesis of (3Z) -5- [ (4,6-dioxy-1,3,5-triazine-2-yl) amino] -4-oxo-3- (benzyl) -3,4-dihydropyrimidine-2,7-diacid is a key research direction in the field of organic chemistry.
To synthesize this compound, the following routes can be tried. First, a series of key reaction steps are carried out through carefully selected reaction conditions and reagents using pyrimidine derivatives containing specific substituents as starting materials. First, modify the specific position on the pyrimidine ring, such as introducing appropriate amino groups, oxygen substitution and other functional groups. This process can be achieved by nucleophilic substitution reaction. In the nucleophilic substitution reaction, it is important to select appropriate nucleophilic reagents and reaction solvents, which can improve the reaction rate and yield.
Furthermore, construct the benzyl substituted part. A suitable benzylation reagent can be used to introduce benzyl at the target position of the pyrimidine ring. This step requires precise regulation of reaction temperature, time and ratio of reactants to prevent side reactions from occurring.
For the construction of dioxy-1,3,5-triazine-2-base parts, a suitable synthesis strategy is also required. Perhaps through a multi-step reaction, the precursor containing this structural unit is first prepared, and then the structure is successfully introduced through steps such as cyclization reaction.
During the entire synthesis process, the control of the reaction conditions and the purification of the intermediate are extremely critical. By selecting appropriate reaction temperature, pressure, catalyst and other conditions, the reaction process can be optimized; and the use of efficient separation and purification technologies, such as column chromatography, recrystallization, etc., can effectively improve the purity of the product. In this way, (3Z) -5- [ (4,6-dioxo-1,3,5-triazine-2-yl) amino] -4-oxo-3- (benzyl) -3,4-dihydropyrimidine-2,7-diacid can be successfully synthesized by carefully designed and manipulated reactions in multiple steps.

(3Z) -5- [ (4,6-dioxy-1,3,5-triazine-2-yl) amino] -4-oxo-3- (benzyl) -3,4-dihydropyrimidine-2,7-dione, the relevant safety precautions for this substance are as follows:
First, this substance is mostly a chemical synthesis product, and the synthesis process often involves a variety of chemical reactions and chemical reagents. Some reagents are corrosive, such as strong acids, strong bases, etc. When operating, be sure to wear comprehensive protective equipment, such as acid and alkali-resistant gloves, protective glasses, and laboratory clothes, etc., to prevent the reagent from contacting the skin and eyes. In case of accidental contact, rinse with plenty of water immediately and seek medical treatment in time.
Second, some reactions may occur under specific conditions, such as high temperature and high pressure. When carrying out such reactions, the reaction conditions should be strictly controlled, and the reaction equipment that meets the standards should be used. Regular inspection and maintenance of the equipment should be carried out to avoid safety accidents caused by equipment failure, such as explosions and other serious situations.
Third, the product itself may have certain toxicity. When operating and using it, it should be carried out in a well-ventilated environment, preferably in a fume hood to prevent inhalation of its dust or volatile gases. If waste is generated during the experiment, it cannot be discarded at will. It should be collected and disposed of in accordance with relevant regulations to avoid pollution to the environment.
Fourth, a comprehensive and in-depth understanding of the properties of the substance, including its stability, compatibility with other substances, etc. Avoid mixing it with incompatible substances to prevent accidental chemical reactions and cause danger. In terms of storage, choose appropriate storage conditions according to its characteristics, such as specific temperature and humidity environments, to ensure its storage safety.