2-Amino-1-benzyl-4,5-dimethyl-1H-pyrrole-3-carbonitrile

Alas! What you say about "2 - Amino - 1 - benzyl - 4,5 - dimethyl - 1H - pyrrole - 3 - carbonitrile" is the name of an organic compound. To understand its chemical structure, it is necessary to analyze it according to the rules of organic chemistry.
This compound is based on a pyrrole ring, which is a five-membered heterocyclic ring containing a nitrogen atom. "1H - pyrrole" is the structure of this pyrrole ring. In the first position of the pyrrole ring, there is a benzyl group (benzyl), and the benzyl group is a benzyl group, which is connected with a benzene ring and a methylene group. < Br >
At the 4th and 5th positions of the pyrrole ring, each is connected with a methyl (methyl), so it is called "4,5-dimethyl". At the 3rd position of the pyrrole ring, there is a cyano group (carbonitrile), and the cyano group is the -CN group. As for "2-Amino", it indicates that at the 2nd position of the pyrrole ring, there is an amino group (-NH2O).
Overall, the chemical structure of this compound is based on the pyrrole ring as the core, and there are benzyl, methyl, cyano and amino groups at specific positions on the ring, respectively. This structure gives it unique chemical properties and reactivity, and may have important application and research value in the fields of organic synthesis, medicinal chemistry, etc.

2-Amino-1-benzyl-4,5-dimethyl-1H-pyrrole-3-formonitrile has a wide range of uses in the fields of medicine and chemical industry.
In the way of pharmaceutical research and development, this compound may be used as a lead compound due to its specific chemical structure and activity. Physicians and pharmacists often modify and optimize this structure to obtain new drugs with better pharmacological activity, higher selectivity and lower toxic and side effects. For example, by fine-tuning the structure of a specific disease-related target, explore its interaction mode with the target to develop innovative drugs for the treatment of diseases such as tumors and inflammation. < Br >
In the chemical industry, it can be used as an intermediary for organic synthesis. Organic synthesis artisans can use its unique structure to construct more complex organic molecular structures through various chemical reactions. Taking the preparation of functional materials as an example, it can be introduced into the polymer structure to endow the material with special electrical, optical or mechanical properties, and then applied to electronic devices, optical materials and other industries. Or in the preparation of fine chemicals, it can be used as a key intermediate to participate in the synthesis of fine chemicals such as fragrances and dyes to enhance their product performance and quality.
Furthermore, in the process of scientific research and exploration, this compound is also an important object for chemical researchers to explore the properties and reaction mechanism of pyrrole compounds. By studying its physicochemical properties, reactivity and selectivity, we can deepen our understanding of pyrrole ring chemistry, contribute to the development of organic chemistry theory, and provide reference for the development of new synthesis methods and strategies.

The synthesis method of 2-amino-1-benzyl-4,5-dimethyl-1H-pyrrole-3-formonitrile has been explored by many parties throughout the ages, and the methods are various.
The common method in the past was obtained by using a specific starting material and going through several steps of reaction. If you choose a basic compound containing nitrogen and carbon, the two will first undergo a condensation reaction to construct the initial shape of the pyrrole ring. In this process, the reaction conditions, such as temperature, pH and reaction time, need to be carefully controlled. If the temperature is too high, it may cause side reactions to multiply and the product is impure; if the temperature is too low, the reaction will be slow and time-consuming.
Or use the method of catalytic reaction. Finding a suitable catalyst can optimize the reaction path, improve the reaction rate and product yield. However, the screening of catalysts is not easy, and its activity, selectivity and stability need to be considered. If the activity is poor, it is difficult to promote the reaction; if the selectivity is insufficient, it is easy to produce side products; if the stability is poor, it will be inactivated in the middle of the reaction, and it will not be able to achieve expectations.
Furthermore, the choice of solvent for organic synthesis is also crucial. Different solvents have different solubility to the reaction substrate, which in turn affects the process of the reaction. Or choose a polar solvent to facilitate the occurrence of ionic reactions; or use a non-polar solvent to adapt to specific nucleophilic and electrophilic reactions.
Nowadays, science and technology are improving, and synthesis methods have also evolved. Or with the help of advanced instruments and equipment, the reaction parameters can be precisely adjusted to achieve efficient and accurate reaction. Or introduce the concept of green chemistry to pursue a more environmentally friendly and sustainable synthesis path, reduce the generation of waste, and reduce the impact on the environment.
Although there are many synthesis methods, each has its own advantages and disadvantages. It is necessary to weigh and consider according to actual needs, and choose the best one to use in order to achieve the desired effect when synthesizing this compound.

2-Amino-1-benzyl-4,5-dimethyl-1H-pyrrole-3-formonitrile is one of the organic compounds. Its physical and chemical properties are worth exploring.
In terms of its physical properties, under normal temperature and pressure, this substance is mostly in a solid state. Looking at its color, it is usually white to off-white powder, with a delicate appearance and a quite pure appearance. The determination of its melting point is crucial in exploring the characteristics of this substance. After experimental determination, its melting point is in a specific temperature range. This temperature value is one of the key physical parameters for the identification of this substance. Because different pure compounds have their own unique melting points.
As for its solubility, this substance has different properties in common organic solvents. In polar organic solvents, such as methanol and ethanol, it has a certain solubility and can form a uniform solution. This property is due to the interaction between the molecular structure and the solvent molecules. The intermolecular forces with similar polarities make the solute better dispersed in the solvent. However, in non-polar organic solvents, such as n-hexane, toluene, etc., the solubility is very small, because the polarity of the molecule is different from that of the non-polar solvent, and the interaction force is weak.
Talking about the chemical properties, the structure of this compound, amino, cyano and pyrrole ring functional groups, endow it with unique chemical activity. The amino group is a nucleophilic group and can participate in a variety of nucleophilic substitution reactions. In case of suitable electrophilic reagents, the nitrogen atom of the amino group can provide electron pairs to attack the electron-deficient center of the electrophilic reagent, and then substitution reactions occur to form new compounds. Cyanyl groups also have high reactivity and can undergo hydrolysis reactions. Under appropriate conditions, cyanyl groups can be gradually converted into carboxyl groups to generate corresponding carboxylic acid compounds. As a conjugated system, pyrrole rings have certain aromatic properties and can participate in electrophilic aromatic substitution reactions. Other functional groups are introduced into the rings to expand the derivation path of compounds. In addition, although the benzyl group is relatively stable, under specific strong oxidation or reduction conditions, corresponding chemical reactions may also occur, resulting in changes in molecular structure.

I look at your question, but I am inquiring about the price range of 2 - Amino - 1 - benzyl - 4,5 - dimethyl - 1H - pyrrole - 3 - carbonitrile in the market. However, the price of this product is difficult to determine. The price often changes for many reasons.
First, its purity has a great impact on the price. If the purity is excellent and impurities are rare, the price will be high; if the purity is slightly inferior, the price may decrease slightly. Second, the supply and demand of the market is also the key. If there are many needs, but the supply is small, the price will rise; conversely, if the supply exceeds the demand, the price will fall. Third, the cost of the system cannot be ignored. The price of raw materials and the simplicity of the process are all related to the cost, which in turn affects the selling price.
In addition, the difference between sellers also results in different prices. Different merchants have different pricing due to differences in business strategies and channels. And the price may also be different due to regional differences.
Therefore, in order to determine the price, it is advisable to consult the chemical product trading platform and consult the chemical raw material supplier to obtain a more accurate price range.