pent-4-enyl 2-(2-furylmethyl-(imidazole-1-carbonyl)amino)butanoate

This is the name of an organic compound. To know its chemical structure, it should be resolved according to the naming rules. "Pent - 4 - enyl" indicates that this compound contains a pentenyl group. The pentenyl group has five carbon atoms and contains a double bond at the fourth carbon atom, that is, $CH_2 = CHCH_2CH_2CH_2 - $.
"2 - (2 - furylmethyl - (imidazole - 1 - carbonyl) amino) butanoate" part, "butanoate" is the butyrate structure, that is, $CH_3CH_2CH (COO - ) -$ 。
"2 - (2 - furylmethyl - (imidazole - 1 - carbonyl) amino) " indicates a substituent attached to the carbon atom at position 2 of the butyrate structure. Where "2 - furylmethyl" refers to 2 - furanmethyl, which is a five-membered heterocycle containing one oxygen atom, and the 2 - furanmethyl structure is a furan ring at position 2 linked $- CH_2 - $.
" (imidazole - 1 - carbonyl) " is imidazole - 1 - carbonyl, imidazole is a five-membered heterocycle containing two nitrogen atoms, and the nitrogen atom at position 1 is connected to the carbonyl $- C (= O )-$ 。“( imidazole - 1 - carbonyl) amino ", that is, imidazole - 1 - carbonyl is connected to the amino group, which is then connected to the 2 - furanomethyl group, and finally connected to the carbon atom at position 2 of the butyrate structure.
In summary, the chemical structure of this compound is pentenyl and is connected to butyrate containing 2-furanomethyl- (imidazole-1-carbonyl) amino group. Although the text is difficult to fully understand its delicacy, according to this analysis, the appearance of the structure can be glimpsed.

Pen-4-enyl-2 - (2 - (furan-2-ylmethyl) (imidazole-1-carbonyl) amino) butyrate, the physical properties of this compound are very important, related to its application and characteristics.
First, the appearance, because of its complex chemical structure, is often presented in solid form, or as a white to light yellow powder substance, this appearance is related to its intermolecular forces and crystalline morphology. Its powder texture is delicate, and under the illumination of light, there is occasional shimmering light, which seems to hide a mysterious light.
As for the melting point, after many experiments, the melting point of this compound is in a specific range, between [X] ° C and [X] ° C. The exact value of the melting point is crucial for judging its state change under different conditions. When the temperature approaches the lower limit of the melting point, the molecules begin to gain enough energy, and the lattice structure gradually loosens; and when the upper limit of the melting point is reached, it melts from a solid state to a liquid state.
Solubility is also a key physical property. In organic solvents, such as common ethanol, dichloromethane, and pentyl-4-enyl-2- (2- (furan-2-ylmethyl) (imidazole-1-carbonyl) amino) butyrate exhibit certain solubility. In ethanol, with the increase of temperature, the dissolution rate is accelerated, and the solubility is also improved. Due to the increase of temperature, the molecular thermal motion is intensified, and the interaction between solvent and solute molecules is enhanced. However, in water, its solubility is poor, which is mainly due to the existence of hydrophobic groups in the molecular structure, which makes the interaction with water molecules weak.
In addition, the density is also the physical property of the compound. Its density is about [X] g/cm ³, which reflects the mass of the substance per unit volume. When it comes to mixture separation or related process design, density data is indispensable and provides an important basis for precise operation.
The physical properties, appearance, melting point, solubility and density of this compound are related to each other, and together they paint a unique physical "portrait", laying a solid foundation for further research and application.

This compound is called pentyl-4-enyl-2- (2- (furan-2-ylmethyl) (imidazole-1-carbonyl) amino) butyrate. It has potential applications in many fields.
In the field of pharmaceutical research and development, due to its unique chemical structure, it may exhibit biological activity. Imidazole and furan groups often have special pharmacological properties, or can regulate the binding of drugs to biological targets. Such as acting on specific enzymes or receptors, or used to develop new antibacterial and anti-inflammatory drugs. From the perspective of traditional medicine, the exploration of the activity of new compounds is like searching for rare fairy grass, adding new paths for treating patients and saving people.
In the field of materials science, this compound may participate in the synthesis of polymer materials. Alkenyl groups can undergo polymerization reactions to build polymer materials, giving materials special properties, such as optical and electrical properties, for the preparation of optoelectronic devices and sensor materials. This is a man-made material, just like ancient skilled craftsmen to create exquisite instruments.
In the field of agriculture, it may be used as the basis for the development of new pesticides. Its structure may inhibit or kill some pests and pathogens, and it is more environmentally friendly and efficient than traditional pesticides. It seems that in ancient times, natural products were used to make insect repellents to protect the growth of crops.
In the field of organic synthesis, it is an important intermediate. Its diverse active groups can be converted through chemical reactions to synthesize more complex compounds, enriching the organic synthesis route, just like building a foundation for complex buildings, paving the way for the development of organic chemistry.

There are many ways to synthesize pent - 4 - enyl 2 - (2 - furylmethyl (imidazole - 1 - carbonyl) amino acid) butanoate.
The first method is to react with 2 - (2 - furanmethyl) imidazole - 1 - formyl chloride and 2 - aminobutyrate - 4 - enyl ester. First, take an appropriate amount of 2- (2-furanomethyl) imidazole-1-formic acid, and convert it to 2- (2-furanomethyl) imidazole-1-formyl chloride at an appropriate temperature and reaction time with a suitable chlorination reagent, such as thionyl chloride. This step should pay attention to the control of reaction conditions to prevent side reactions. In addition, pentyl-4-enyl 2-aminobutyrate can be prepared by reacting 2-aminobutyric acid with pentyl-4-enol in a suitable organic solvent such as dichloromethane in the presence of a condensing agent such as dicyclohexyl carbodiimide (DCC) and a catalyst 4-dimethylaminopyridine (DMAP). The obtained 2 - (2-furanomethyl) imidazole-1-formyl chloride was slowly added to the solution of 2-aminobutyrate amyl-4-enyl ester, and the reaction was stirred at low temperature to room temperature. After the reaction is completed, the target product can be obtained by extraction, washing, drying, column chromatography and other purification steps. The
sub-method can be directly condensed by 2 - (2-furanomethyl) imidazole-1-carboxylic acid and 2-aminobutyrate amyl-4-enyl ester under the action of a condensing agent. The combination of 1 - (3 - dimethylaminopropyl) - 3 - ethylcarbodiimide hydrochloride (EDC · HCl) and 1 - hydroxybenzotriazole (HOBt) is selected in an organic solvent, the two are mixed, adjusted to a suitable pH value, and the reaction is stirred at room temperature. The reaction process is monitored by thin layer chromatography (TLC). After the reaction, the target product is separated by conventional purification operations such as extraction and washing.
Furthermore, the amino group of 2 - aminobutyrate - 4 - enyl ester can be protected first, such as the protective group such as tert-butoxycarbonyl (Boc). After protection, it is reacted with 2- (2-furylmethyl) imidazole-1-formyl chloride to remove the protecting group. Although this process has many steps, it can effectively reduce side reactions and improve the purity of the product. After similar purification methods, pure pent-4-enyl-2- (2-furylmethyl (imidazole-1-carbonyl) amino) butanoate can also be obtained.

The discussion on the market prospect of pent - 4 - enyl + 2 - (2 - furylmethyl - (imidazole - 1 - carbonyl) amino) butanoate is related to the development of chemical and pharmaceutical industries.
In the chemical industry, such organic compounds are often the cornerstone of the synthesis of exquisite molecules. Nowadays, the chemical process is increasingly refined, and there is a hunger for high-purity and high-performance raw materials. The unique structure of this compound may emerge in the creation of new materials. Its unsaturated bond and heterocyclic structure can endow the material with specific physical and chemical properties, such as enhanced flexibility and improved thermal stability. Therefore, under the wave of advanced materials research and development, it is expected to gain a place in the chemical market, just like a jade waiting to be carved, and the potential is hidden.
As for the pharmaceutical industry, heterocyclic structures such as imidazole are often biologically active. This compound may be modified and modified to become a key component in the development of targeted drugs. As the concept of precision medicine takes root, the demand for specific drugs has surged. If pent - 4 - enyl + 2 - (2 - furylmethyl - (imidazole - 1 - carbonyl) amino) butanoate can exhibit specific pharmacological activities, such as anti-cancer, anti-inflammatory, etc., pharmaceutical companies must compete to study, and the market prospect is limitless.
However, its market expansion is not smooth. The complexity of the synthesis process may lead to high production costs, limiting its large-scale production and application. And the market competition is fierce, and similar compounds are also competing. To come out on top, researchers need to devote themselves to research, optimize the process, reduce costs and increase efficiency, in order to ride the wave of the market and open up broad prospects.