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Fluorenone oxime

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Identification
Molecular formula
C13H9NO
CAS number
1660-65-1
IUPAC name
fluoren-9-one oxime
State
State

At room temperature, fluorenone oxime is a solid. It maintains structural integrity and does not exhibit any phase changes or notable malleability until exposed to higher temperatures where it transitions to other states.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
195.22g/mol
Molar mass
195.2280g/mol
Density
1.2288g/cm3
Appearence

Fluorenone oxime appears as a light yellow crystalline solid. It has a distinctive appearance that is characteristic of many organic oxime derivatives. Its bright yellow crystals are often quite striking and are typically utilized in various chemical synthesis applications.

Comment on solubility

Solubility of Fluoren-9-one Oxime

Fluoren-9-one oxime, with the chemical formula C13H11NO, shows interesting solubility characteristics that are essential for various applications.

Generally, the solubility of fluoren-9-one oxime can be described as:

  • Solvent Dependency: Fluoren-9-one oxime tends to be more soluble in organic solvents, such as dichloromethane and ethanol, owing to its hydrophobic fluorenyl structure.
  • Limited Aqueous Solubility: Its solubility in water is quite limited because of its nonpolar characteristics, which hinder interactions with polar water molecules.
  • Temperature Effects: Like many organic compounds, its solubility may increase with temperature, making it more effective in warmer conditions.

As noted, “solubility is fundamentally influenced by the interactions at a molecular level.” Thus, while fluoren-9-one oxime displays a definite preference for nonpolar environments, understanding its solubility profile is crucial for its use in synthesis and chemical reactions.

In conclusion, fluoren-9-one oxime's solubility behavior is not only a reflection of its molecular structure but also plays a significant role in its practical applications and chemical reactivity.

Interesting facts

Interesting Facts about Fluoren-9-one Oxime

Fluoren-9-one oxime, an organic compound derived from the well-known fluorenone, offers numerous intriguing characteristics that make it a significant subject of study in the field of chemistry. This compound is particularly notable for its applications in various industries and research disciplines.

Key Characteristics and Applications

  • Versatile Intermediary: Fluoren-9-one oxime serves as an important intermediate in the synthesis of more complex organic molecules, making it a valuable building block in organic chemistry.
  • Analytical Reagent: This compound is often used as a reagent in analytical chemistry, especially in the detection of certain metal ions.
  • Potential Biological Activity: Preliminary studies have suggested that fluoren-9-one oxime may exhibit biological activities, sparking interest in its potential applications in pharmaceuticals.
  • Applications in Material Science: Its unique structural properties have made it a subject of interest in the development of luminescent materials and polymers.
  • Storage Stability: The compound is known for its stability under various conditions, which can be advantageous in both experimental and industrial settings.

Chemical Reaction Insights

When studying fluoren-9-one oxime, one fascinating aspect is its ability to undergo various reactions, particularly:

  • Nucleophilic Substitution: The oxime functional group allows for significant nucleophilic activity, which can lead to the formation of diverse derivatives.
  • Isomerization: This compound can also participate in isomerization reactions, emphasizing the importance of understanding its structural reactivity.

In summary, fluoren-9-one oxime is more than just a compound; it is a gateway to exploring complex organic syntheses and potential applications in various fields. As one insightful chemist once said, "In every molecule lies a story waiting to be unraveled," and fluoren-9-one oxime is undoubtedly a captivating chapter in the narrative of organic chemistry.

Synonyms
9-Fluorenone oxime
2157-52-0
Fluorenone oxime
fluoren-9-one oxime
NSC 1988
EINECS 218-471-8
BRN 1871046
DTXSID50175919
4-07-00-01631 (Beilstein Handbook Reference)
DTXCID1098410
crnnfekvprfzkj-uhfffaoysa-n
9H-Fluoren-9-one oxime
N-fluoren-9-ylidenehydroxylamine
9-Oximinofluorene
Fluorenone-9-oxime
FLUOREN-9-ONE, OXIME
9H-Fluoren-9-one, oxime
MFCD00016356
BQN5AH5VZJ
MLS001181444
NSC-1988
SMR000567249
N-(9H-FLUOREN-9-YLIDENE)HYDROXYLAMINE
9H-Fluoren-9-oneoxime
SR-01000390929
fluorenonoxim
9-Fluorenone, oxime
UNII-BQN5AH5VZJ
CBDivE_014646
SCHEMBL577391
N-hydroxy-9H-fluoren-9-imine
CHEMBL1492999
NSC1988
N-fluoren-9-ylidene-hydroxylamine
HMS1577D07
HMS2870P13
STK387446
AKOS001062418
AC-4875
CS-W015721
DS-6618
FF70110
SB67052
NCGC00246633-01
SY049700
DB-080838
F0023
NS00026906
EN300-15688
H11335
AE-641/02574026
SR-01000390929-1
SR-01000390929-3
Z49568437