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N-(9,10-dihydrophenanthren-2-yl)acetamide

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Identification
Molecular formula
C16H15NO
CAS number
15456-96-1
IUPAC name
N-(9,10-dihydrophenanthren-2-yl)acetamide
State
State

At room temperature, N-(9,10-dihydrophenanthren-2-yl)acetamide is in a solid state. It exhibits a crystalline structure which indicates a well-ordered arrangement at the molecular level.

Melting point (Celsius)
122.00
Melting point (Kelvin)
395.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
239.30g/mol
Molar mass
239.3010g/mol
Density
1.1700g/cm3
Appearence

This compound typically appears as a white crystalline solid. It may have a faint aromatic odor, which is characteristic of many organic compounds containing aromatic groups.

Comment on solubility

Solubility of N-(9,10-dihydrophenanthren-2-yl)acetamide

N-(9,10-dihydrophenanthren-2-yl)acetamide is a compound that exhibits intriguing solubility characteristics, which are influenced by its chemical structure. Here are key aspects to note regarding its solubility:

  • Polarity: The presence of the acetamide functional group may enhance its polarity, potentially allowing for better solubility in polar solvents like water.
  • Hydrophobic nature: The phenanthrene moiety is largely hydrophobic, which could limit its solubility in aqueous solutions.
  • Solvent selection: It is likely to be more soluble in organic solvents such as ethanol and dimethyl sulfoxide (DMSO) due to the non-polar character of the aromatic ring.
  • Temperature effects: Solubility may also be affected by temperature changes, as higher temperatures generally increase solubility in most solvents.

In summary, while N-(9,10-dihydrophenanthren-2-yl)acetamide may exhibit some degree of solubility in polar solvents, its overall hydrophobic characteristics could lead to relatively limited solubility in water. This complex behavior highlights the importance of considering both polar and non-polar interactions when evaluating solubility. As noted, the choice of solvent plays a crucial role in the behavior of this compound in solution.

Interesting facts

Interesting Facts about N-(9,10-dihydrophenanthren-2-yl)acetamide

N-(9,10-dihydrophenanthren-2-yl)acetamide is a fascinating compound that has garnered attention in various fields of research, especially in organic chemistry and medicinal chemistry.

Key Characteristics and Applications

  • Structure and Stability: The structure of this compound incorporates a phenanthrene moiety, which contributes to its unique properties. The fused ring system offers stability and potentially interesting electronic characteristics.
  • Potential Medicinal Applications: Compounds like N-(9,10-dihydrophenanthren-2-yl)acetamide may exhibit biological activity, making them of interest in drug discovery and development. Researchers are exploring their effects on various biological pathways.
  • Fluorescence Properties: The intriguing structure can lead to specific fluorescence properties, prompting investigations into its use in optical applications or as a probe in biochemical studies.
  • Research Significance: This compound represents a synthetic approach in organic chemistry that can lead to derivatives with enhanced properties, thus paving the way for innovative chemical syntheses.

Historical Context and Future Directions

In the world of chemistry, structures derived from polycyclic aromatic hydrocarbons (PAHs) have been extensively studied due to their relevance in both environmental and biological contexts. As we continue to refine our understanding of compounds like N-(9,10-dihydrophenanthren-2-yl)acetamide, we may uncover more about their roles in chemical reactions and potential applications in therapeutics.

As one researcher remarked, “The beauty of organic chemistry lies not only in its complexity but in the endless possibilities it presents for innovation.” This compound is a perfect example of that sentiment, symbolizing the intersection of creativity and science.

In summary, N-(9,10-dihydrophenanthren-2-yl)acetamide serves as a beacon in the landscape of chemical research, inviting scientists to explore its properties and applications further. The ongoing studies will certainly shed light on its capabilities and broaden our understanding of similar compounds.

Synonyms
18264-88-5
Acetamide, N-(9,10-dihydro-2-phenanthryl)-
BRN 2978862
2-Acetylamino-9,10-dihydrophenanthrene
N-(9,10-DIHYDRO-2-PHENANTHRYL)ACETAMIDE
DTXSID90171314
3-12-00-03316 (Beilstein Handbook Reference)
DTXCID4093805
N-(9,10-dihydrophenanthren-2-yl)acetamide
Maybridge3_000517
Oprea1_144051
MLS001181466
CHEMBL1517894
SCHEMBL28448285
HMS1432H11
HMS2863N09
CCG-55491
IDI1_011904
NCGC00246629-01
SMR000567231
NS00016267
SR-01000644513-1
BRD-K81429389-001-07-4