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Thiophene-2-methyl ketoxime

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Identification
Molecular formula
C6H7NOS
CAS number
49851-33-2
IUPAC name
1-(2-thienyl)ethanone oxime
State
State

This compound is typically in a solid state at room temperature.

Melting point (Celsius)
55.00
Melting point (Kelvin)
328.15
Boiling point (Celsius)
281.80
Boiling point (Kelvin)
554.95
General information
Molecular weight
141.19g/mol
Molar mass
141.1870g/mol
Density
1.1135g/cm3
Appearence

1-(2-Thienyl)ethanone oxime typically appears as a yellow to orange solid. It may exist in a crystalline form, depending on the conditions of its synthesis and purification.

Comment on solubility

Solubility of 1-(2-thienyl)ethanone oxime

1-(2-thienyl)ethanone oxime exhibits interesting solubility characteristics that are noteworthy for both practical applications and theoretical studies. This compound is known to be moderately soluble in various organic solvents, which makes it amenable to a range of chemical processes.

Factors Affecting Solubility

The solubility of 1-(2-thienyl)ethanone oxime can be influenced by:

  • Polarity: The presence of the oxime functional group contributes to some polar characteristics, enhancing solubility in polar solvents.
  • Temperature: As with many organic compounds, an increase in temperature often leads to increased solubility.
  • Solvent Choice: This compound is known to dissolve well in solvents such as ethanol and dichloromethane, but may be less soluble in non-polar solvents.

In practical usage, the solubility of 1-(2-thienyl)ethanone oxime is often exploited in the synthesis of derivatives and in various chemical reactions. As a result, understanding its solubility behavior can be crucial for optimizing reaction conditions.

In conclusion, while 1-(2-thienyl)ethanone oxime is not as widely recognized for its solubility compared to some other compounds, its unique characteristics and interactions with different solvents provide valuable insights for researchers and practitioners in the field.

Interesting facts

Interesting Facts about 1-(2-Thienyl)ethanone Oxime

1-(2-Thienyl)ethanone oxime is a fascinating compound that showcases unique characteristics and applications in various fields. Here are some intriguing points about this compound:

  • Structure and Bonding: The presence of the thienyl group, derived from thiophene, introduces a sulfur atom into the aromatic ring, altering the compound's reactivity and electronic properties compared to similar ketones.
  • Dynamic Applications: This compound is not just a theoretical interest; it has potential applications in the field of organic synthesis, particularly in the formation of more complex molecules through various reactions.
  • Oxime Functionality: As an oxime, the compound can participate in a variety of chemical reactions, including rearrangement and condensation reactions, making it a versatile building block in medicinal chemistry.
  • Research Potential: The specific arrangement of atoms and functional groups in 1-(2-thienyl)ethanone oxime provides fertile ground for research, particularly in exploring its biological activity and possible pharmaceutical applications.
  • Electronic Properties: The delocalization of electrons in the thienyl ring may influence its properties, lending interest to studies in materials science where electron mobility is critical.

As scientists continue to explore the myriad uses and effects of 1-(2-thienyl)ethanone oxime, it becomes ever clearer that this compound stands out as more than just a simple molecule—it embodies complexities that can lead to important discoveries in chemistry and beyond.

Synonyms
ethanone, 1-(2-thienyl)-, oxime, (1Z)-
N-(1-thiophen-2-ylethylidene)hydroxylamine
1956-45-2
N-[1-(thiophen-2-yl)ethylidene]hydroxylamine
methyl thienyl ketone oxime
(E)-N-[1-(THIOPHEN-2-YL)ETHYLIDENE]HYDROXYLAMINE
SCHEMBL2907543
1-(thiophen-2-yl)ethanone oxime
DTXSID80941341
HODHTVIKKXGOCP-UHFFFAOYSA-N
AKOS017263164
DB-015307
NS00046027