CAS 1468-82-2

2-bromo-1-(3-thienyl)-1-ethanone

Description:

2-Bromo-1-(3-thienyl)-1-ethanone is an organic compound characterized by its unique structure, which includes a bromine atom and a thienyl group attached to an ethanone moiety. This compound typically appears as a yellow to brown solid and is known for its reactivity due to the presence of the bromine atom, which can participate in various substitution reactions. The thienyl group, derived from thiophene, contributes to the compound's aromatic properties and can influence its electronic characteristics, making it useful in various chemical applications, including synthesis and as an intermediate in organic reactions. The presence of the carbonyl group (ketone) in the ethanone structure adds to its reactivity, allowing it to undergo nucleophilic addition reactions. Additionally, 2-bromo-1-(3-thienyl)-1-ethanone may exhibit biological activity, making it of interest in medicinal chemistry. As with many brominated compounds, it is essential to handle it with care due to potential toxicity and environmental concerns.

Formula: C₆H₅BrOS

InChI: InChI=1/C6H5BrOS/c7-3-6(8)5-1-2-9-4-5/h1-2,4H,3H2

SMILES: c1cscc1C(=O)CBr

Synonyms:

• 2-Bromo-1-Thiophen-3-Ylethanone

Ethanone, 2-bromo-1-(3-thienyl)-

CAS: 1468-82-2

Formula: C₆H₅BrOS

Purity: 95%

Color and Shape: Solid

Molecular weight: 205.0723

Ref: IN-DA001ECN

2-Bromo-1-(3-thienyl)-1-ethanone

CAS: 1468-82-2

2-Bromo-1-(3-thienyl)-1-ethanone is a useful organic compound for research related to life sciences.

Formula: C₆H₅BrOS

Color and Shape: Solid

Molecular weight: 205.072

Ref: TM-T125824

3-(Bromoacetyl)thiophene

CAS: 1468-82-2

3-(Bromoacetyl)thiophene

Formula: C₆H₅BrOS

Purity: 95%

Color and Shape: solid

Molecular weight: 205.07g/mol

Ref: 54-OR23201

2-Bromo-1-(thiophen-3-yl)ethanone

CAS: 1468-82-2

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 205.07000732421875

Ref: 10-F034082

3-(Bromoacetyl)thiophene

CAS: 1468-82-2

3-(Bromoacetyl)thiophene is a chromophore that can be used as an antibacterial agent. It has potent inhibitory effects on bacteria, which are caused by the ring-opening of the thiophene ring in the presence of irradiation. 3-(Bromoacetyl)thiophene can also be used in electrochemical polymerization and cyclic voltammetry. In addition, it has been shown to have an inhibitory effect on dehydrogenase enzymes, which are important for energy production in cells. This compound is fluorescent and can be detected using electrochemical impedance spectroscopy (EIS).

Formula: C₆H₅BrOS

Purity: Min. 95%

Molecular weight: 205.07 g/mol

Ref: 3D-BAA46882