2-Amino-4-methyl-1H-pyrrole-3-carbonitrile

2-Amino-4-methyl-1H-pyrrole-3-formonitrile is an organic compound. It has specific chemical properties and is often used as a key intermediate in the field of organic synthesis.
In terms of its chemical properties, the amino group in this compound is basic and can react with acids to form corresponding salts. Nitrile groups are also active functional groups and can participate in various chemical reactions, such as hydrolysis to obtain carboxylic acid derivatives, or conversion to amines by reduction. Pyrrole rings are aromatic, which affects their chemical activity and reaction selectivity.
In physical properties, under normal temperature and pressure, 2-amino-4-methyl-1H-pyrrole-3-formonitrile is mostly solid, but its specific melting point, boiling point, etc., depend on its purity and crystalline morphology. Its solubility may be certain in common organic solvents, such as ethanol and dichloromethane, but its solubility in water or limited by molecular polarity is relatively low.
This compound has a wide range of uses in the field of organic synthetic chemistry due to the coexistence of various functional groups in its structure. Complex organic molecular structures can be constructed through various reaction pathways, providing important starting materials and synthetic building blocks for the creation of drugs, materials, and other fields, and assisting the development and preparation of new substances.

The common synthesis methods of 2-amino-4-methyl-1H-pyrrole-3-formonitrile cover a variety of. One is to use a suitable starting material to construct a pyrrole ring through a multi-step reaction and introduce the desired functional group. Usually, the compounds containing nitrogen and carbon sources are taken first, and the condensation reaction occurs under specific conditions. For example, in an appropriate catalyst and temperature and solvent environment, the nitrogen-containing compounds interact with the carbon sources containing carbonyl or alkenyl groups to initially form a pyrrole skeleton.
Or use a cyclization reaction strategy, select a chain or cyclic precursor with suitable substituents, and construct a pyrrole structure through intramolecular cyclization. This process requires precise regulation of reaction conditions, such as pH, reaction time and temperature, to ensure the smooth progress of cyclization and the formation of the target product.
Furthermore, the reaction path of metal catalysis can be used. Metal catalysts can effectively promote the formation and fracture of chemical bonds, facilitate the construction of pyrrole rings, and introduce functional groups such as amino groups, methyl groups, and cyanos. Under metal catalysis, reactions such as coupling and addition occur between substrates to gradually realize the synthesis of target molecules. In the
synthesis process, each step of the reaction needs to be carefully controlled to separate, purify and identify the reaction products to ensure that the reaction proceeds in the direction of generating 2-amino-4-methyl-1H-pyrrole-3-formonitrile, and to ensure that the purity and yield of the product meet expectations.

2-Amino-4-methyl-1H-pyrrole-3-formonitrile is used in many fields. In the field of medicinal chemistry, its role is particularly important. Because of its unique chemical structure, it can be used as a key intermediate to synthesize drug molecules with specific biological activities. In the research and development of many antibacterial and antiviral drugs, it is often relied on as a starting material to build complex drug structures through a series of chemical reactions to achieve the effect of treating diseases and saving people.
In the field of materials science, 2-amino-4-methyl-1H-pyrrole-3-formonitrile also has wonderful uses. It can participate in the preparation of functional materials, such as some optoelectronic materials. After ingenious design and synthesis, it becomes a part of the material structure, endowing the material with unique optoelectronic properties, and is used to manufacture new optoelectronic devices, such as organic Light Emitting Diodes, which contribute to the development of materials science.
Furthermore, in the field of organic synthetic chemistry, it is a very commonly used synthetic building block. Organic chemists use this as a basis to build complex and diverse organic compounds by virtue of various organic reactions, such as nucleophilic substitution, cyclization reactions, etc., which greatly enriches the variety of organic compounds, promotes the continuous progress of organic synthetic chemistry, and provides more material basis for the development of various fields.

2-Amino-4-methyl-1H-pyrrole-3-formonitrile, this is an organic compound. Its physical properties are unique, let me tell you one by one.
Looking at its appearance, it is mostly white to light yellow crystalline powder under normal conditions. This is due to the characteristics of its molecular structure, which is caused by the interaction between molecules to form this shape. The powder has a fine texture and a relatively uniform particle distribution.
When it comes to the melting point, it is about a specific temperature range. Because the atoms in the molecule are closely connected by covalent bonds, a stable structure is formed. When heated, it needs to absorb enough energy to overcome the intermolecular forces in order to disintegrate its lattice structure and realize the transition from solid to liquid. This melting point is of great significance for maintaining its physical state in different environments.
In terms of solubility, it exhibits a certain solubility in common organic solvents, such as ethanol and dichloromethane. Because the compound molecule has a specific polarity, it can form interactions such as hydrogen bonds and van der Waals forces with organic solvent molecules, so that it can be dispersed in the solvent. However, in water, its solubility is poor, because the polarity of water molecules matches the polarity of the compound molecule with limited polarity, and the interaction is weak.
Furthermore, its density is also an important physical property. The value of density reflects the degree of close packing of molecules, which is affected by the size, shape and arrangement of molecules. Its density determines the space occupied in a specific environment and the distribution state when mixed with other substances.
In addition, the compound has certain stability and can maintain its own structure under normal conditions. However, under extreme conditions such as strong acids, strong bases or high temperatures, the molecular structure may change, resulting in changes in its physical properties. This is because under extreme conditions, the chemical bonds within the molecule may be broken, triggering structural rearrangement or chemical reactions.
The above are the main physical properties of 2-amino-4-methyl-1H-pyrrole-3-formonitrile, which are related to each other and jointly determine the behavior of this compound in different scenarios.

I look at your question, but I am inquiring about the market price of 2-amino-4-methyl-1H-pyrrole-3-formonitrile. However, the price of this chemical often changes for many reasons, which is difficult to determine.
First, the impact of the production source is quite large. If it comes from a well-known and well-crafted large factory, the price may be slightly higher due to excellent quality and stability; if it is made by a small factory, the price may be relatively low.
Second, the supply and demand situation determines the price. If the market faces strong demand for this product and limited supply, the price will rise; conversely, if the supply is abundant and the demand is insufficient, the price will drop.
Third, the price of raw materials is also the key. The synthesis of this chemical depends on specific raw materials. If the price of raw materials rises, the price of finished products will also rise accordingly; if the price of raw materials falls, the price of finished products may also be lowered.
Fourth, the place of sales is different from the channel, and the price is also different. In prosperous cities, due to high logistics and operating costs, the price may be high; through online platforms, there are no many intermediate links, and the price may be favorable.
And the market conditions are changing rapidly. If you want to know the exact price, you should consult chemical product suppliers, distributors, or professional chemical trading platforms to find the current accurate price.