1-{(E)-2-(methylsulfanyl)-1-[2-(pentyloxy)phenyl]ethenyl}-1H-imidazole

This is to investigate the chemical structure of 1- { (E) -2- (methylthio) -1- [2- (pentoxy) phenyl] vinyl} -1H -imidazole. The imidazole ring is the core structure of this compound, and a specific substituent is attached to the 1 position. The substituent is composed of (E) -2- (methylthio) -1- [2- (pentoxy) phenyl] vinyl. It can be seen from " (E) " that this vinyl part is in the trans configuration. Among them, 2 - (methylthio) means that there is a methylthio (-SCH) group attached to the second position of the vinyl group. And 1 - [2 - (pentoxy) phenyl] indicates that the first position of the vinyl group is connected to a benzene ring, and the second position of the benzene ring is connected with a pentoxy group (-O - C H). In the pentoxy group, the pentyl group (C H) is a straight chain or a pentacaralkyl structure with different branches. In this chemical structure, each atom and group are connected by specific chemical bonds to form a unique spatial arrangement, giving the compound specific physical and chemical properties, which may be of great significance in chemical synthesis, drug development and other fields.

1 - { (E) - 2 - (methylsulfanyl) - 1 - [2 - (pentyloxy) phenyl] ethenyl} - 1H - imidazole is an organic compound. The physical properties of this substance are crucial for its application in various scenarios.
First of all, its appearance is usually solid, but the exact color state may vary depending on the purity and preparation method. Either it is white crystalline and has a fine texture; or it is slightly colored, depending on the presence or absence of impurities.
Secondary melting point, this is an important physical property. The exact melting point needs to be determined experimentally, but it can be speculated that, in view of its molecular structure containing aromatic rings and heterocycles, the mutual force is strong, and the melting point is not extremely low. The presence of benzene rings and imidazole rings in the molecule makes the molecules packed tightly, requiring higher energy to destroy the lattice, so the melting point may be within the range of common organic solids, or between tens and two or three hundred degrees Celsius.
Furthermore, when it comes to solubility, because it contains hydrophobic alkyl groups (pentoxy groups) and thiomethyl groups, its solubility in polar organic solvents such as methanol and ethanol may be limited. However, in non-polar or weakly polar organic solvents such as dichloromethane, chloroform, and toluene, the solubility may be relatively better. Due to the principle of similar phase dissolution, the non-polar part interacts with the non-polar solvent, which facilitates its dissolution.
In addition, the boiling point is also an important consideration. In the same way as the melting point, due to the intermolecular force, the boiling point may be higher. To make it boil, it is necessary to provide enough energy to overcome the attractive force between molecules.
The density of this substance is also significant. Although the exact value is difficult to accurately predict with the structure, it is probably comparable to that of common organic compounds. Because the atoms of carbon, hydrogen, nitrogen, and sulfur in the molecule form a specific structure, they are given a certain relationship between mass and volume, which determines the density range.
The physical properties of 1- { (E) -2- (methylsulfanyl) -1- [2- (pentyloxy) phenyl] ethenyl} -1H -imidazole, such as appearance, melting point, solubility, boiling point, density, etc., play an important guiding role in its application in chemical synthesis, materials science, drug development and other fields. Researchers can carry out related work according to these properties.

1 - { (E) - 2 - (methylsulfanyl) - 1 - [2 - (pentyloxy) phenyl] ethenyl} - 1H - imidazole, an organic compound, has important uses in many fields due to its unique structure.
In the field of medicine, such compounds containing imidazole structures often exhibit diverse biological activities. The imidazole ring can interact with many targets in organisms, such as certain proteins and enzymes. The specific structure of this compound may give it high affinity and selectivity for specific disease-related targets. Or it can be used to develop new antimicrobial drugs, by interfering with key bacterial metabolic processes or cell wall synthesis to achieve antibacterial purposes; or as a potential anticancer drug, by inhibiting the proliferation of tumor cells and inducing their apoptosis to play an effect.
In the field of materials science, its structure endows certain electronic properties and stability, or it can be used to prepare functional materials. For example, in organic optoelectronic materials, it may be able to regulate the charge transport and optical properties of materials, and be used in organic Light Emitting Diodes (OLEDs), solar cells and other devices to improve their performance.
In the field of agriculture, such compounds may serve as precursor structures for the creation of pesticides. With its ability to interfere with the physiological processes of certain pests or pathogens, new insecticides and fungicides have been developed to assist agricultural pest control, and may have higher efficiency and lower environmental toxicity than traditional pesticides.
In summary, 1- { (E) -2- (methylsulfanyl) -1- [2- (pentyloxy) phenyl] ethenyl} -1H - imidazole has potential application value in the fields of medicine, materials science, agriculture, etc. With in-depth research, it is expected to bring new opportunities for the development of various fields.

To obtain 1 - { (E) - 2 - (methylsulfanyl) - 1 - [2 - (pentyloxy) phenyl] ethenyl} - 1H - imidazole, the following method can be followed.
First take 2 - (pentyloxy) benzaldehyde and methylsulfanylacetonitrile as starting materials. In an alkaline environment, the two will undergo Knoevenagel condensation reaction. Basic reagents can be selected such as piperidine, heated and stirred in a suitable solvent such as ethanol. In this step, the aldehyde group of 2 - (pentyloxy) benzaldehyde is condensed with the active methylene group of methylsulfanylacetonitrile, resulting in (E) - 2 - (methylsulfanyl) - 1 - [2 - (pentyloxy) phenyl] acrylonitrile.
Then, the obtained (E) - 2 - (methylsulfanyl) - 1 - [2 - (pentyloxy) phenyl] acrylonitrile is reacted with imidazole. This reaction needs to be carried out in the presence of a suitable catalyst, for example, a basic catalyst such as potassium carbonate can be selected, in a suitable organic solvent, such as N, N - dimethylformamide (DMF), and heating prompts the reaction to occur. In this reaction process, the nitrogen atom of imidazole will perform nucleophilic addition to the carbon-carbon double bond of (E) -2- (methylsulfanyl) -1- [2- (pentyloxy) phenyl] acrylonitrile. After a series of reactions, the target product 1 - { (E) -2- (methylsulfanyl) -1 - [2- (pentyloxy) phenyl] ethenyl} -1H - imidazole. During the
reaction process, close attention should be paid to the control of the reaction conditions. Temperature, reaction time, and the proportion of reactants all have significant effects on the yield and selectivity of the reaction. For example, during the Knoevenagel condensation reaction, if the temperature is too low, the reaction rate will be slow, and if it is too high, it may lead to an increase in side reactions. In the subsequent reaction with imidazole, the amount of catalyst, reaction temperature and time also need to be precisely controlled in order to make the reaction efficient and selectively carried out well, in order to obtain the target product with higher yield.

1 - { (E) - 2 - (methylthio) - 1 - [2 - (pentoxy) phenyl] vinyl} - 1H -imidazole This product is related to many safety precautions, let me elaborate.
First of all, this chemical may have certain toxicity. It enters the human body, or through inhalation, skin contact and accidental ingestion. Inhalation, or irritate the respiratory tract, causing cough, asthma, breathing difficulties and other symptoms; skin contact, or cause allergies, redness, swelling, itching and other reactions; if accidentally ingested, it may damage the stomach, causing nausea, vomiting, abdominal pain and other symptoms. Therefore, when handling this object, be sure to wear protective clothing, protective gloves and masks, and beware of contact with it.
Furthermore, its chemical properties or activity. Under certain conditions, or react violently with other substances, and even cause an explosion. When storing, keep away from fire, heat and strong oxidants, place in a cool, dry and well-ventilated place, and keep it separate from other chemicals to prevent interaction.
At the same time, disposal also needs to be cautious. It must not be discarded at will, and should be handed over to professional institutions in accordance with relevant regulations, so as to avoid pollution to the environment.
In addition, the place where this object is operated needs to be well ventilated to reduce its concentration in the air. And it should be equipped with emergency treatment equipment, such as eye washers, spray devices, etc., in case of an accident, it can be responded to in time.
In short, when using 1 - { (E) - 2 - (methylthio) - 1 - [2 - (pentoxy) phenyl] vinyl} - 1H - imidazole, every step needs to be taken with extreme care and operated in strict accordance with safety procedures to ensure personnel safety and the environment are not endangered.