cas 39565-00-9|| where to buy 1-(5-Nitrothiophen-2-yl)ethanone

Nombre del producto:1-(5-Nitrothiophen-2-yl)ethanone

IUPAC Name:1-(5-nitrothiophen-2-yl)ethan-1-one

: CAS：39565-00-9; Fórmula molecular：C6H5NO3S; Pureza：95%

: Número de catálogo：CM252712; Peso molecular：171.17

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CM252712-1g	in stock	ƃŞ

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Detalles del producto

: Núm. De CAS :39565-00-9; Fórmula molecular:C6H5NO3S; Punto de fusión:-; Código de sonrisas:O=[N+](C1=CC=C(C(C)=O)S1)[O-]; Densidad:

: Número de catálogo:CM252712; Peso molecular:171.17; Punto de ebullición:; Nº Mdl:MFCD00041211; Almacenamiento:

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.

Product Other Information

Product Overview	2-Acetyl-5-nitrothiophene (2-AN) is a synthetic, organic compound with a wide range of biological applications. It is an aromatic heterocyclic compound, which is composed of a five-membered ring containing two carbon atoms, one nitrogen atom and two sulfur atoms.
Synthesis Method	The most common method involves the reaction of 5-nitrothiophene-2-carboxylic acid with an amine, such as aniline, in the presence of a base. The reaction produces 2-Acetyl-5-nitrothiophene and an amide byproduct. Other methods of synthesis include the reaction of 5-nitrothiophene-2-carboxylic acid with an alcohol or aldehyde in the presence of a base, or the reaction of 5-nitrothiophene-2-carboxylic acid with an acid chloride in the presence of a base.
Chemical Properties	One of the main advantages is that it is relatively inexpensive and easy to synthesize. Additionally, it has a wide range of biological activities. However, 2-Acetyl-5-nitrothiophene is also limited by its low solubility in aqueous solutions and its instability in the presence of light and heat.
Synthesis and Application	2-Acetyl-5-nitrothiophene is widely used as a research tool in biochemistry and physiology. In vivo and in vitro studies have been conducted to investigate the biological activities of 2-Acetyl-5-nitrothiophene. In vivo studies involve the administration of 2-Acetyl-5-nitrothiophene to animals or humans to observe its effects on the body. In vitro studies involve the use of cell cultures or isolated enzymes to study the effects of 2-Acetyl-5-nitrothiophene on biochemical or physiological processes.
Future Directions	Further investigations into the mechanism of action of 2-Acetyl-5-nitrothiophene and its potential therapeutic applications. Development of new synthetic methods for the synthesis of 2-Acetyl-5-nitrothiophene. Development of new derivatives of 2-Acetyl-5-nitrothiophene with improved pharmacokinetic properties.Investigation of the potential of 2-Acetyl-5-nitrothiophene as an anticancer agent.