Название продукции:Ethyl 2-amino-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate

IUPAC Name:ethyl 2-amino-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate

CAS:174072-89-0
Молекулярная формула:C14H14N2O4S
Чистота:95%+
Номер в каталоге:CM301846
Молекулярная масса:306.34

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Информация о продукции

Номер CAS:174072-89-0
Молекулярная формула:C14H14N2O4S
Точка плавления:-
Smiles-код:O=C(C1=C(N)SC(C2=CC=C([N+]([O-])=O)C=C2)=C1C)OCC
Плотность:
Номер в каталоге:CM301846
Молекулярная масса:306.34
Точка кипения:464.596°C at 760 mmHg
Номер Mdl:
Хранение:Keep in a tight container and store at ambient temperature

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

Column Infos

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Product Other Information

Product Overview Ethyl 2-amino-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate, often referred to as EMN-TPC, is a novel compound that has recently been studied for its potential applications in various scientific research fields. EMN-TPC has been demonstrated to possess a wide range of biochemical and physiological effects, including anti-inflammatory and anti-cancer properties.
Synthesis and Application EMN-TPC can be synthesized via a two-step process. First, the compound is synthesized from 4-nitrophenyl thiophene-3-carboxylic acid and ethyl amine. This reaction is catalyzed by a base, such as sodium hydroxide, and occurs in an ethanol or methanol solvent. The second step involves the condensation of the product of the first step with ethyl 2-amino-4-methyl-5-nitrophenylthiophene-3-carboxylate. This reaction is catalyzed by a strong acid, such as hydrochloric acid, and occurs in a toluene or ethyl acetate solvent. EMN-TPC has been studied for its potential applications in various scientific research fields. It has been demonstrated to possess anti-inflammatory and anti-cancer properties, and has been used to study the role of inflammation in the development of cancer. It has also been used to study the mechanisms of drug resistance in cancer cells. Additionally, EMN-TPC has been studied for its potential to inhibit the growth of harmful bacteria, and has been used to study the role of bacterial biofilms in the development of infections.
Future Directions There are several potential future directions for research into EMN-TPC. First, further research is needed to determine the exact mechanism of action of the compound. Additionally, further research is needed to determine the potential therapeutic applications of EMN-TPC, such as its potential use as an anti-inflammatory or anti-cancer drug. Additionally, further research is needed to determine the potential toxicity of EMN-TPC, and to develop methods to reduce the potential toxicity of the compound. Finally, further research is needed to determine the potential applications of EMN-TPC in other scientific fields, such as in the study of bacterial biofilms.