Product Name:1-(5-Nitrothiophen-2-yl)ethanone

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

CAS:39565-00-9
Molecular Formula:C6H5NO3S
Purity:95%
Catalog Number:CM252712
Molecular Weight:171.17

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Product Details

CAS NO:39565-00-9
Molecular Formula:C6H5NO3S
Melting Point:-
Smiles Code:O=[N+](C1=CC=C(C(C)=O)S1)[O-]
Density:
Catalog Number:CM252712
Molecular Weight:171.17
Boiling Point:
MDL No:MFCD00041211
Storage:

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.