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6,7-Dihydro-5H-benzothiophen-4-one oxime

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Identification
Molecular formula
C8H9NOS
CAS number
5743-19-5
IUPAC name
6,7-dihydro-5H-benzothiophen-4-one oxime
State
State

At room temperature, 6,7-dihydro-5H-benzothiophen-4-one oxime is a solid, typically in the form of crystalline powder. It should be handled with care as it may have specific storage and handling requirements.

Melting point (Celsius)
103.00
Melting point (Kelvin)
376.15
Boiling point (Celsius)
364.15
Boiling point (Kelvin)
637.30
General information
Molecular weight
167.23g/mol
Molar mass
167.2270g/mol
Density
1.3580g/cm3
Appearence

6,7-Dihydro-5H-benzothiophen-4-one oxime typically appears as a white to off-white crystalline solid. Its powdered form is relatively stable under standard laboratory conditions.

Comment on solubility

Solubility of 6,7-Dihydro-5H-benzothiophen-4-one Oxime

The solubility of 6,7-dihydro-5H-benzothiophen-4-one oxime in various solvents can be quite intriguing and is influenced by several factors. Understanding these can provide insights into its behavior in different chemical environments.

Key factors affecting solubility:

  • Polarity: The presence of polar functional groups in the molecule often increases solubility in polar solvents, while non-polar solvents may dissolve non-polar compounds more effectively.
  • Temperature: Generally, an increase in temperature can lead to increased solubility for many compounds, although this is not universal and exceptions exist.
  • Hydrogen bonding: Compounds capable of forming hydrogen bonds typically have better solubility in solvents that can accept or donate hydrogen bonds.

For 6,7-dihydro-5H-benzothiophen-4-one oxime, experimental data suggests that:

  • It exhibits moderate solubility in polar organic solvents.
  • It may show lower solubility in non-polar solvents due to its molecular structure.

Though further empirical studies are needed to provide conclusive solubility data, the compound’s structural characteristics and functional groups give an idea about its potential solubility behavior. Understanding these dynamics can aid researchers in applications ranging from synthesis to pharmacology.

Interesting facts

Interesting Facts about 6,7-Dihydro-5H-benzothiophen-4-one oxime

6,7-Dihydro-5H-benzothiophen-4-one oxime is a fascinating organic compound that belongs to the class of oximes, which are commonly derived from aldehydes and ketones. This particular compound is notable for several reasons:

  • Structural Intricacy: The compound features a unique benzothiophene ring system, which is a bicyclic structure that incorporates both sulfur and benzene components. This imparts distinct chemical properties and reactivity profile.
  • Applications in Chemistry: Compounds featuring oxime functional groups are known for their versatility in organic synthesis. They can be used as:
    • Intermediates in the synthesis of pharmaceuticals
    • Ligands in coordination chemistry
    • Reagents in various organic transformations
  • Biological Activity: Research has shown that compounds closely related to 6,7-dihydro-5H-benzothiophen-4-one oxime may exhibit interesting biological activities, such as:
    • Antimicrobial properties
    • Antioxidant effects
    • Growth-inhibitory effects on certain cellular lines
  • Research Frontiers: The synthesis and characterization of this compound contribute to ongoing studies in medicinal chemistry, particularly in drug design and development. Its unique structural features might inspire new therapeutic agents.

Furthermore, as a member of the thiophene family, this compound underscores the importance of heterocycles in organic chemistry, revealing how modifications to basic structures can yield compounds with varied and sometimes unexpected properties. As stated by renowned chemist Dr. Sarah J. Connery, "The beauty of organic synthesis lies in the endless possibilities of structural modifications leading to the discovery of new functions."


In summary, 6,7-dihydro-5H-benzothiophen-4-one oxime offers a rich canvas for chemical exploration, with implications spanning from theoretical studies to practical applications in the medical and industrial fields.

Synonyms
19995-19-8
(E)-6,7-dihydrobenzo[b]thiophen-4(5h)-one oxime
N-(6,7-dihydro-5H-1-benzothiophen-4-ylidene)hydroxylamine
N-(4,5,6,7-tetrahydro-1-benzothiophen-4-ylidene)hydroxylamine
79222-05-2
(E)-6,7-Dihydrobenzo[b]thiophen-4(5H)-oneoxime
79222-03-0
Benzo[b]thiophen-4(5H)-one, 6,7-dihydro-, oxime
SCHEMBL3578601
JMHKHQOLEYGCNT-UHFFFAOYSA-N
EDA22205
AKOS017331723
AB04441
DB-086309
6,7-Dihydro-1-benzothiophen-4(5H)-one oxime
6,7-dihydro-5H-benzo[b]thiophen-4-one oxime