Skip to main content

N-(9H-fluoren-2-yl)hydroxylamine

ADVERTISEMENT
Identification
Molecular formula
C13H11NO
CAS number
85636-18-0
IUPAC name
N-(9H-fluoren-2-yl)hydroxylamine
State
State

At room temperature, N-(9H-fluoren-2-yl)hydroxylamine is in a solid state. It is crystalline in nature and stable under standard conditions.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.15
Boiling point (Celsius)
392.00
Boiling point (Kelvin)
665.15
General information
Molecular weight
197.24g/mol
Molar mass
197.2370g/mol
Density
1.2000g/cm3
Appearence

N-(9H-fluoren-2-yl)hydroxylamine typically appears as a crystalline solid at room temperature. It usually has a white to off-white color.

Comment on solubility

Solubility of N-(9H-fluoren-2-yl)hydroxylamine

N-(9H-fluoren-2-yl)hydroxylamine, with the chemical formula C13H11NO, exhibits some interesting characteristics regarding its solubility.

Generally, the solubility of N-(9H-fluoren-2-yl)hydroxylamine can be influenced by various factors:

  • Polarity of the Compound: This compound has a polar hydroxylamine functional group that can interact favorably with polar solvents.
  • Choice of Solvent: It is likely to be soluble in organic solvents such as ethanol and methanol, but may display limited solubility in non-polar solvents.
  • Temperature Dependence: Solubility often increases with temperature, making higher temperatures potentially beneficial for dissolving this compound.

As with many organic compounds, it's essential to test solubility experimentally as theoretical predictions can vary greatly. As a general observation, "the presence of functional groups such as -OH significantly enhances solubility in polar environments". Proper assessment will ensure the most effective use in various applications.

Interesting facts

Interesting Facts about N-(9H-fluoren-2-yl)hydroxylamine

N-(9H-fluoren-2-yl)hydroxylamine is a fascinating compound that falls within the category of organic compounds known as hydroxylamines. This specific compound showcases the unique blend of aromatic and amine characteristics.

Key Features:

  • Aromatic Structure: The compound features a fluorenyl group, a result of a fused aromatic system, which provides stability and enhances reactivity.
  • Biological Relevance: Hydroxylamines, including N-(9H-fluoren-2-yl)hydroxylamine, are often studied for their potential pharmacological applications, particularly in the development of pharmaceutical agents.
  • Versatile Reactivity: Hydroxylamines can participate in various chemical reactions, such as diazotization and coupling reactions, making them valuable in synthetic organic chemistry.

One of the striking aspects of N-(9H-fluoren-2-yl)hydroxylamine is its involvement in the field of materials science. The compound can be used to create novel polymeric materials through reactions with different monomers. Additionally, its ability to function as a reducing agent in certain reactions amplifies its importance.

Applications and Importance:

  • Research in Organic Chemistry: The compound serves as a model for studying reaction mechanisms involving hydroxylamines.
  • Colorimetric Indicators: Its derivatives are explored as colorimetric reagents, aiding in analytical procedures.
  • Environmental Monitoring: Hydroxylamines can be used in environmental chemistry to detect and quantify pollutants.

As a compound, N-(9H-fluoren-2-yl)hydroxylamine presents significant opportunities for exploration in both academic and industrial settings. Its intriguing structure and versatile chemistry invite chemists to think critically about its applications and involve it in various chemical syntheses.

Synonyms
N-Hydroxy-2-aminofluorene
53-94-1
N-(9H-fluoren-2-yl)hydroxylamine
9H-Fluoren-2-amine, N-hydroxy-
N-Hydroxy-N-2-aminofluorene
N-Hydroxy-aminofluorene
2-Fluorenylhydroxylamine
N-Fluorene-2-yl-hydroxylamine
2-(Hydroxyamino)fluorene
N-Hydroxy-2-fluorenamine
HSDB 2113
N-2-Fluorenylhydroxylamine
CCRIS 1067
Hydroxylamine, N-fluoren-2-yl-
BRN 2722130
UNII-61M94X4V24
DTXSID50201045
HYDROXY-2-AMINOFLUORENE, N-
61M94X4V24
N-FLUORENE-2-YL-HYDROXYLAMINE [HSDB]
N-2-hydroxyaminofluorene
NHydroxyaminofluorene
NHydroxy2fluorenamine
NHydroxy2aminofluorene
2Fluorenylhydroxylamine
NHydroxyN2aminofluorene
N2Fluorenylhydroxylamine
2(Hydroxyamino)fluorene
starbld0042967
9HFluoren2amine, Nhydroxy
Hydroxylamine, Nfluoren2yl
CHEMBL314422
SCHEMBL3095573
DTXCID50123536
NS00115892
Q27263358