Chemical Formula | C14H14N2O4S |
Molar Mass | 306.34 g/mol |
Appearance | Solid (usually, but color may vary) |
Physical State At Room Temp | Solid |
Solubility In Water | Low (organic compounds with this structure are typically sparingly soluble in water) |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
What are the chemical properties of 2-Amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester
This is 2-amino-4-methyl-5- (4-nitrophenyl) thiophene-3-carboxylic acid ethyl ester, which has unique chemical properties.
Let's talk about the appearance first. At room temperature, it is mostly in the state of off-white to light yellow crystalline powder. It is like a fine powder and has a uniform texture.
When it comes to solubility, it has a certain solubility in organic solvents, such as dichloromethane, N, N-dimethylformamide, etc., but it has little solubility in water. This characteristic is due to the hydrophobic group in its molecular structure. Both nitrophenyl and thiophene rings are hydrophobic, making it difficult to dissolve in water with strong polarity.
Besides stability, in the conventional environment, if there are no special conditions, it is still stable. However, in case of strong acid or strong base, the structure may be damaged. In case of strong acid, amino group or protonation, its chemical activity is affected; in case of strong base, ester group or hydrolysis, the molecular structure is changed.
Talking about reactivity, amino groups can participate in a variety of reactions, such as reacting with acid chlorides to form amides, which is an important way to construct compounds containing amide bonds in organic synthesis; ester groups can be hydrolyzed, alcoholyzed, and aminolyzed, and corresponding carboxylic acids can be obtained by hydrolysis. Different esters can be obtained by alcoholysis, and aminolysis can be obtained by aminolysis. Although the thiophene ring is aromatic, it can also participate in the electrophilic substitution reaction. Under suitable conditions, nitrophenyl can affect its reaction check point and activity.
This compound is of great significance in the field of organic synthesis and can be used as an intermediate. It can be prepared by a series of reactions with biological activity or special functions. It has potential application value in the creation of medicine and pesticides.
What are the synthesis methods of 2-Amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester
The synthesis method of 2-amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester, although the synthesis of this compound is not described in the ancient book "Tiangong Kaiwu", the ancient chemical technology thinking and similar synthesis methods may be used for reference.
In the past, esters were synthesized, often using carboxylic acids and alcohols as raw materials, and were prepared by esterification. To obtain this compound, 2-amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid can be prepared first, and then reacted with ethanol under the action of a catalyst.
Synthesis of 2-amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid, which can be derived from thiophene derivatives containing corresponding substituents. Functional groups such as amino and carboxyl groups are introduced through multi-step reactions. For example, with suitable thiophene starters, nitrophenyl groups are first introduced, and then the groups at specific positions are converted into amino and carboxyl groups through ingenious reactions.
After obtaining 2-amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid, using concentrated sulfuric acid as a catalyst, co-heating with ethanol, esterification reaction occurs, and the target product 2-amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester can be obtained. This process requires attention to the control of reaction conditions, such as temperature, reactant ratio, reaction time, etc., to improve yield and purity. Although not entirely based on ancient methods, this synthesis can be achieved by leveraging ancient chemical thinking and modern chemical knowledge.
What is the main use of 2-Amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester
2-Amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester, which has a wide range of uses. In the field of medicinal chemistry, it is often used as a key intermediate. Due to its unique chemical structure, it can be modified by various chemical reactions to synthesize compounds with specific pharmacological activities, such as the development of new antibacterial and anti-tumor drugs, etc., making great contributions to human health.
In the field of organic synthetic chemistry, it is also an important cornerstone. It can use a variety of organic reactions and combine with different reagents to build complex organic molecular structures, which can help synthesize many functional materials and be used in the field of materials science, such as the preparation of materials with special optical and electrical properties.
In addition, it may also play an important role in pesticide chemistry. After structural optimization and modification, new pesticides with high efficiency, low toxicity and environmental friendliness may be developed, which is crucial for agricultural pest control, can effectively improve crop yield and quality, and maintain sustainable agricultural development.
In summary, 2-amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylate ethyl ester plays an important role in many fields such as medicine, materials, and pesticides, and is of great significance to promoting scientific and technological progress and industrial development in various fields.
What is the market price of 2-Amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester
I look at your question, and I am inquiring about the market price of 2-amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester. However, the market price of this compound is difficult to determine. The change in its price depends on many factors.
The first one to bear the brunt is the difficulty of production. If the synthesis method is complicated, rare raw materials and harsh reaction conditions are required, the cost will be high, and the price will rise accordingly. On the contrary, if the preparation method is simple, the raw materials are easy to find and inexpensive, the price may be accessible.
Furthermore, the state of market supply and demand is also the key. If the demand for this product is strong and the supply is limited, such as for the preparation of special drugs, high-end materials, etc., the demand far exceeds the supply, and the price will rise. On the contrary, if the market demand is low and the supply is abundant, the price may decline.
In large-scale production, due to the scale effect, the unit production cost may be reduced, and the price is expected to be more reasonable. Small-scale production is more expensive, making it difficult to drop the price.
In addition, the state of market competition cannot be ignored. If multiple manufacturers produce this product, the competition is fierce, and in order to compete for market share, the price may be reduced. On the contrary, if the market is monopolized, the price can be higher.
Therefore, in order to determine the market price of this compound, it is necessary to carefully observe the production, supply and demand, scale, competition and other conditions, and comprehensively consider, in order to obtain a more accurate price.
What are the storage conditions for 2-Amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester?
2-Amino-4-methyl-5- (4-nitro-phenyl) thiophene-3-carboxylic acid ethyl ester, this is an organic compound. Its storage is mainly in a low temperature environment. Due to high temperature, it is easy to cause its chemical properties to change, or accelerate the process of decomposition. It should be placed in a refrigerated environment of two to eight degrees, so that its structure can be stable and its long-term storage will remain unchanged.
Furthermore, it must be protected from light. Under light, the compound or photochemical reaction will damage its purity and quality. When in an opaque container, such as a brown glass bottle, hide in a dark place and avoid direct sunlight.
and keep dry. Moisture or lead to reactions such as hydrolysis, which can damage its chemical properties. Where it is stored, the humidity should be controlled at a low level, or a desiccant should be built into the storage container to absorb moisture and keep it dry.
Also, this compound may have certain toxicity and danger. When storing, keep it away from fire and heat sources, it is flame-proof and explosion-proof. And it should be placed separately from oxidants, acids, alkalis, etc., to avoid chemical reactions and lead to safety. When taking it, it should also follow strict operating procedures to ensure personal and environmental safety.