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1-(benzothiophen-3-yl)ethanone

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Identification
Molecular formula
C10H8OS
CAS number
4209-48-9
IUPAC name
1-(benzothiophen-3-yl)ethanone
State
State

At room temperature, 1-(benzothiophen-3-yl)ethanone is in a solid state. It is typically presented as a powder or in crystal form depending on the purity and synthesis method.

Melting point (Celsius)
91.00
Melting point (Kelvin)
364.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
174.23g/mol
Molar mass
174.2300g/mol
Density
1.2123g/cm3
Appearence

1-(Benzothiophen-3-yl)ethanone appears as a pale yellow to light tan crystalline solid. The compound usually forms needle-like crystals and is known for its aromatic odor due to the benzothiophene moiety. It may also appear slightly granular depending on the method of crystallization and purification.

Comment on solubility

Solubility of 1-(benzothiophen-3-yl)ethanone

The solubility of 1-(benzothiophen-3-yl)ethanone is influenced by several factors, including its molecular structure and the presence of functional groups. This compound, characterized by its unique aromatic system, exhibits varying solubility characteristics in different solvents.

Solubility Characteristics:

  • Polar Solvents: It is generally less soluble in polar solvents such as water, due to the hydrophobic nature of the benzothiophene ring.
  • Non-Polar Solvents: The compound shows greater solubility in non-polar solvents like hexane or dichloromethane, where the aromatic interactions are favorable.
  • Miscibility: It does not mix well with highly polar solvents, which limits its applications in aqueous environments.

In essence, the solubility behavior of 1-(benzothiophen-3-yl)ethanone reflects its complex interactions based on polarity and molecular structure. Knowing this can help in selecting appropriate solvents for reactions or formulations involving this compound.

Interesting facts

Interesting Facts about 1-(benzothiophen-3-yl)ethanone

1-(benzothiophen-3-yl)ethanone is a fascinating organic compound that has captured the interest of chemists and biochemists alike due to its unique structural characteristics and potential applications.

Structural Insights

This compound features a benzothiophene moiety, which is notable for its:

  • Heterocyclic structure: The presence of sulfur in the ring contributes to its reactivity and unique electronic properties.
  • Planar configuration: This allows for effective π-π stacking interactions, which can enhance its properties in various applications.

Potential Applications

Research into 1-(benzothiophen-3-yl)ethanone has revealed several intriguing potential applications:

  • Pharmaceuticals: Compounds containing benzothiophene derivatives are often investigated for their biological activities, including anti-cancer and anti-inflammatory properties.
  • Materials Science: The unique electronic properties may pave the way for use in organic electronic devices or as sensors.

Chemical Reactions

The compound can undergo various chemical transformations, making it valuable for synthetic chemistry. Some notable reactions include:

  • Electrophilic substitution: The aromatic ring can readily undergo reactions with electrophiles, allowing for the exploration of structure-activity relationships.
  • Oxidation and reduction: The compound's functional groups allow for versatile redox chemistry, which can be useful in organic synthesis.

Scientific Quote

As chemist and educator Linus Pauling once said, "The best way to have a good idea is to have lots of ideas." This rings true in the study of compounds like 1-(benzothiophen-3-yl)ethanone, where the exploration of its diverse properties could lead to groundbreaking discoveries.

In summary, the study of 1-(benzothiophen-3-yl)ethanone is not merely academic; it presents unique challenges and opportunities in both chemical research and practical applications, making it an exciting area of focus for scientists today.

Synonyms
3-Acetylbenzothiophene
1-(1-Benzothiophen-3-Yl)Ethan-1-One
DTXSID2074457
DTXCID3033303
846-931-3
3-Acetylthianaphthene
1128-05-8
3-Acetylbenzo[b]thiophene
3-Acetylthionaphthene
1-(benzo[b]thiophen-3-yl)ethanone
3-Acetyl benz[b]thiophene
KETONE, METHYL 3-THIANAPHTHENYL
3-Acetylbenzo(b)thiophene
3-Acetyl benzothiophene
1-(1-benzothiophen-3-yl)ethanone
Ethanone, 1-benzo(b)thien-3-yl-
Ethanone, 1-benzo[b]thien-3-yl-
NSC 3226
1-(Benzo[b]thiophen-3-yl)ethan-1-one
AI3-18374
1-Benzo[b]thiophen-3-yl-ethanone
Ketone, benzo[b]thien-3-yl methyl
MFCD00051638
Ketone, benzo(b)thien-3-yl methyl
NSC-3226
BRN 0122587
3-acetyl thianaphthene
3-acetylbenzo[b]thiophen
YQ9UT5BNM9
5-17-10-00173 (Beilstein Handbook Reference)
WLN: T56 DSJ BV1
CHEMBL564835
SCHEMBL1095746
1-(1-Benzothien-3-yl)ethanone
1-(1-benzothiene-3-yl)ethanone
NSC3226
1-(1-Benzothien-3-yl)ethanone #
Ethanone, 1-benzo[b]thiophen-3-yl-
AKOS005202893
BS-23037
SY061561
DB-046853
CS-0132288
NS00010764
EN300-111010
F81484
Z370714364