1-AMINO-2-CYANOPYRROLE

1-Amino-2-cyanopyrrole, which is a crucial compound in the field of organic synthesis, has a wide range of uses and is described as follows:
First, in the field of medicinal chemistry, its role is significant. It is a key intermediate in many drug development. The structure of this compound has unique activity and can interact with specific targets in vivo. For example, in the creation of some anti-tumor drugs, 1-amino-2-cyanopyrrole can be used as a starting material for the construction of structural units with targeted inhibition of tumor cell proliferation activity. Through a series of organic reactions, it is connected with other functional groups to design and synthesize new anti-tumor drugs with high efficiency and low toxicity.
Second, in the field of materials science, it also has its application. It can be used to participate in the preparation of organic materials with special properties. For example, in the synthesis of optoelectronic materials, the introduction of 1-amino-2-cyanopyrrole into the polymer structure can change the electron cloud distribution of the material, thereby adjusting the optical and electrical properties of the material. The prepared materials can be applied to optoelectronic devices such as organic Light Emitting Diodes (OLEDs) to improve the luminous efficiency and stability of the devices.
Third, in the field of synthesis of heterocyclic compounds, 1-amino-2-cyanopyrrole is often used as a key building block. Due to the unique combination of pyrrole rings with amino groups and cyano groups, complex and diverse heterocyclic compounds can be constructed through various cyclization reactions, nucleophilic substitution reactions, etc. These heterocyclic compounds have indispensable applications in the total synthesis of natural products and new pesticides and veterinary drugs.
Fourth, in the study of organic synthesis methodologies, 1-amino-2-cyanopyrrole is often used as a model substrate. Scientists study the chemical reactions they participate in, explore new reaction paths, and optimize reaction conditions, thus developing more efficient and green organic synthesis methods, promoting the continuous progress of organic chemistry.

1 - AMINO - 2 - CYANOPYRROLE is an organic compound, and its physical properties are worth exploring. This substance is mostly solid at room temperature, and it is usually white to light yellow crystalline powder. This color and morphology are conducive to preliminary identification. Its melting point is in a specific range, about [X] ° C. This melting point characteristic is extremely critical in the identification and purification of substances. Its purity can be judged by melting point measurement.
Furthermore, 1 - AMINO - 2 - CYANOPYRROLE has different solubility in different solvents. In polar solvents such as methanol and ethanol, it has a certain solubility. Because the molecular structure contains polar groups, it can form intermolecular forces with polar solvents, such as hydrogen bonds, so it can be soluble. However, in non-polar solvents such as n-hexane, the solubility is very small, because the non-polar structure is incompatible with the polar structure of 1-AMINO-2-CYANOPYRROLE.
Its density is also an important physical property, about [X] g/cm ³, and the density value is instructive for material separation, storage and related chemical operations. And this material has certain stability, and it is not easy to spontaneously undergo chemical reactions under conventional conditions. However, under extreme conditions such as high temperature and strong acid and alkali, the structure may change, triggering chemical reactions. This property needs to be considered in practical application to ensure safety and product quality.

1 - AMINO - 2 - CYANOPYRROLE is one of the organic compounds. The stability of its chemical properties depends on many factors and cannot be generalized.
Looking at the structure of this compound, the amino group and the cyano group are connected to the pyrrole ring. The amino group has certain electron-giving properties, and the cyano group has electron-withdrawing properties, and the two interact on the pyrrole ring. The pyrrole ring itself is an electron-rich aromatic system, but the electron cloud distribution is changed due to the substitution of the amino group and the cyano group.
Under normal circumstances, 1 - AMINO - 2 - CYANOPYRROLE may have certain stability. The atoms in its structure are connected by covalent bonds to form a relatively stable structure. In case of special conditions, such as high temperature, strong acid-base or specific oxidants and reducing agents, the stability may be challenged.
Under high temperature, the thermal motion of the molecule intensifies, the vibration of the covalent bond is enhanced, or the bond is broken. In a strongly acidic environment, the amino group or protonation changes the electron cloud distribution of the molecule, which in turn affects its stability; in a strongly alkaline environment, the cyano group may undergo reactions such as hydrolysis, disrupting the original structure of the molecule.
As for the redox reaction, the amino group or the cyano group can be used as a reaction check point to participate in the reaction, causing the molecular structure to change and the stability to be lost. The chemical stability of 1-AMINO-2-CYANOPYRROLE depends on the specific conditions, and it is not absolutely stable or unstable. Under suitable conditions, it may maintain a relatively stable state; however, under extreme conditions, its structure and properties are prone to change.

The synthesis method of 1-amino-2-cyanopyrrole has always had its own advantages and disadvantages. In the past, it may have been based on ancient methods and followed the old system. The first method is to start with a specific pyrrole derivative, and through a fine chemical reaction, the amino group and the cyano group are cleverly added to the specific position of the pyrrole. First take the pyrrole parent body, use a suitable reagent, under a specific reaction condition, such as at a certain temperature and pressure, activate it in one position, and then introduce the cyanide group. This step requires precise control of the reaction temperature. If it is slightly worse, it is prone to side reactions of disproportionation. After the cyanide group is firmly attached, the amino group is introduced with other reagents and conditions, and the reaction is exquisite, just like the tenon-mortise fit. If there is a little carelessness, the synthesis road will be tortuous and difficult.
Another method is to start from the basic organic raw materials and use a delicate design to construct the target molecule through a multi-step series reaction. The starting material is condensed, cyclized and other reactions to gradually build a pyrrole skeleton. In this process, the timing and method of introducing amino and cyano groups are particularly critical. For example, during cyclization, cyanide-containing structural fragments are ingeniously introduced, and then in subsequent steps, they are accurately converted into cyano groups, and at the right time, the amino groups are ingeniously connected with unique reagents. This process is like carving beautiful jade. Each knife needs to be just right to obtain pure 1-amino-2-cyanopyrrole.
There are also modern new methods as the path. With the help of advanced catalytic technology, the reaction can be made more efficient and precise. For example, the use of specific metal catalysts can accelerate the reaction process under mild reaction conditions and improve the selectivity of the product. This metal catalyst is like a magic wand, guiding the direction of the reaction, so that the amino group and the cyano group, like a smart dancer, fall precisely on the pyrrole according to the designed dance steps to synthesize the desired product. And modern methods often focus on green and sustainable, and strive to have mild reaction conditions, reduce the generation of waste, make the synthesis process both efficient and environmentally friendly, and open up a new world for the synthesis of 1-amino-2-cyanopyrrole.

The market price of 1-amino-2-cyanopyrrole is difficult to determine. This is due to a number of reasons, resulting in volatile price fluctuations.
The first to bear the brunt is the price of raw materials. If the price of 1-amino-2-cyanopyrrole is determined by Wright due to changes in weather, origin, and supply and demand, the price of 1-amino-2-cyanopyrrole will also move. For example, if the raw material production area encounters disasters and the output of raw materials decreases, its price will rise, and the production cost of 1-amino-2-cyanopyrrole will increase, and the market price will also rise.
Furthermore, the preparation method and cost also affect its price. The exquisite and efficient method can reduce the cost, the price or the people; if the preparation process is complicated, the energy consumption is large, and the high-priced catalyst or reagent is required, the cost will be high and the price will also be high.
In addition, the market supply and demand is the key to the price. If the demand for 1-amino-2-cyanopyrrole is high in many industries, but the production and supply are limited, the price will rise; on the contrary, if the demand is low and the production and supply are excessive, the price will decline.
In addition, different places have different prices due to differences in taxes, logistics fees, and market competition. Prosperous cities, due to convenient logistics, large market, or intense competition, the price may be relatively reasonable; remote places, due to logistics inconvenience, high cost, or slightly high price.
To sum up, if you want to know the current market price of 1-amino-2-cyanopyrrole, you should consult chemical raw material suppliers, distributors, or professional chemical product information platforms to obtain a more accurate price.