Chemical Formula | C16H16N2O4S |
Appearance | Solid (predicted) |
Boiling Point | Predicted around 486.4°C at 760 mmHg |
Melting Point | Predicted to be in a certain range (experimental needed for exact value) |
Density | Predicted value (experimental determination required for accurate density) |
Solubility | Insoluble in water, soluble in some organic solvents like DMSO, DMF |
Flash Point | Predicted around 248.9°C |
Refractive Index | Predicted value (experimental determination needed for exact refractive index) |
Pka | No common pKa data available (acid - base properties depend on environment) |
What is the chemical structure of ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate
Alas! This is an organic chemical substance named "ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate". To clarify its chemical structure, it is necessary to analyze the group referred to in its name.
"ethyl", ethyl is also an alkyl group containing two carbons, expressed in -C ² H, which is often connected to the main structure as a substituent. "2 - amino" epiamino (-NH2O) is connected to the second position of the thiophene ring. "4 - methyl" shows that the methyl group (-CH 😉) is in the fourth position of the thiophene ring.
In "5 - (4 - nitrophenyl) ", 4 - nitrophenyl is a nitrophenyl group, and the nitro group (-NO 2) is in the para-position of the benzene ring, and the phenyl group is attached to the fifth position of the thiophene ring.
"3 - thiophenecarboxylate" indicates that the thiophene ring is connected with a carboxylic acid ethyl ester group (-COOCH 2 CH) in the third position, which is obtained by forming an ester of carboxylic group and ethanol.
In summary, this compound takes the thiophene ring as the backbone and is connected with an amino group, methyl group, nitrophenyl group and carboxylic acid ethyl ester group at a specific position in the ring. Its structure is exquisite and the wonders of organic chemistry are revealed. From this perspective, this compound has a complex structure and unique chemical properties, which may be of great use in organic synthesis and related fields.
What are the physical properties of ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate
Ethyl-2-amino-4-methyl-5- (4-nitrophenyl) -3-thiophene carboxylic acid ester, the physical properties of this substance are as follows:
View its shape, often in the shape of a solid powder, and the color may be white or light yellow. Its melting point is quite critical, and the melting point is about a specific range. This value is the inherent characteristics of the substance and is related to its phase transition. When the temperature rises to the melting point, the substance gradually melts from the solid state to the liquid state, and this process requires the absorption of specific heat. The boiling point also has a certain value. When the temperature reaches the boiling point, the liquid substance will transform into a gaseous state, which is also closely related to the intermolecular forces. < Br >
In terms of solubility, in organic solvents, such as ethanol and acetone, there may be a certain solubility. Due to the molecular structure and polarity of organic solvents, or the interaction between the molecules of the substance, such as van der Waals force, hydrogen bonding, etc., it can partially dissolve. However, in water, due to the difference in molecular polarity from water, the solubility may be very small.
Density is also one of its physical properties. This value reflects the mass per unit volume of a substance and is related to its physical behavior in a specific environment. < Br >
In addition, this substance may have a specific refractive index. When light passes through the substance, the direction and speed of light propagation change, and the refractive index characterizes this property, which is of great significance in optical related research and applications.
These physical properties are important factors to consider when synthesizing, separating, purifying, and applying to chemical, pharmaceutical, and other fields.
What is the main use of ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate
Ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate is an organic compound, Chinese name or 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) - 3 - thiophenecarboxylate ethyl ester. Its main use is quite extensive, in the field of medical chemistry, often used as a key intermediate. Through specific chemical reactions, its structure can be modified and modified to synthesize compounds with specific pharmacological activities, or used to develop drugs for the treatment of specific diseases.
In the field of materials science, the compound may participate in the preparation of materials with special properties due to its unique chemical structure and properties. For example, some groups in its structure may interact with other materials to improve the properties of materials, such as enhancing the stability of materials and changing the optical properties of materials.
In the field of pesticides, it also has potential application value. Through rational design and modification, pesticide products with high insecticidal, bactericidal or herbicidal activities may be developed to assist in the control of pests and diseases and weeds in agricultural production, so as to improve the yield and quality of crops.
This compound is often used as a model compound in many aspects of chemical research, such as the study of organic synthesis methodologies, to help researchers explore new reaction pathways and synthesis strategies, and to promote the development of organic chemistry.
What are the synthesis methods of ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate
Today, there are compounds ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate. The synthesis method is quite complicated, and it is necessary to follow the rules of organic synthesis and select suitable raw materials and steps.
First, sulfur-containing heterocyclic compounds can be selected as starting materials, such as 2 - methyl - 3 - carboxylthiophene. After acylation, a suitable acylating agent is used to convert the carboxyl group into an ethyl group. This step requires controlling the reaction conditions, such as temperature and catalyst dosage.
Secondly, for the substitution on the thiophene ring, nucleophilic substitution or electrophilic substitution reaction can be used to introduce amino groups. In this process, appropriate amination reagents should be selected to pay attention to the selectivity of the reaction and prevent side reactions.
Furthermore, 4-nitrophenyl group can be introduced through arylation reaction. Choose 4-nitrohalobenzene with suitable activity and use palladium catalysis or other metal catalysis systems to promote its connection to the thiophene ring. During the reaction, the choice of solvent and the amount of base are all related to the effectiveness of the reaction.
To synthesize this compound, the conditions of each step of the reaction need to be precisely controlled. The purity of the raw material, the temperature of the reaction, time, catalyst and other factors have a significant impact on the yield and purity of the product. The synthesis process requires patience and meticulous, and careful operation of multiple steps can be expected to obtain the target compound ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate.
Ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate what to pay attention to when storing and transporting
Ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate, the Chinese name is roughly 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) thiophene - 3 - carboxylic acid ethyl ester. When storing and transporting this material, many matters need to be paid attention to.
First, it is related to storage. Because of its nature or more active, it needs to find a cool, dry and well-ventilated place. Do not place it in a high temperature place to prevent excessive temperature from causing chemical reactions or triggering decomposition, which will damage its quality. It should not be placed in a humid place. Moisture may cause it to deteriorate and affect its chemical structure and properties. It should be stored separately from oxidants, acids, alkalis, etc., to avoid dangerous chemical reactions caused by mixed storage. The storage place should be clearly marked, indicating the name, characteristics and precautions of this thing, so that it can be used and managed.
Second, as for transportation. During transportation, be sure to ensure that the container is well sealed to prevent leakage. Choose suitable means of transportation, and the transportation equipment should have the functions of high temperature, rain protection and sun protection. During the handling process, the operation should be handled lightly, and must not be handled brutally, so as not to cause damage to the packaging and cause material leakage. Transport personnel also need to be familiar with the characteristics of this object and emergency treatment methods. In case of emergencies, they can respond quickly and correctly. At the same time, the transportation documents should be complete and the relevant information of this object should be recorded in detail for inspection. In this way, ethyl 2 - amino - 4 - methyl - 5 - (4 - nitrophenyl) -3 - thiophenecarboxylate is safe during storage and transportation.