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[acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate

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Identification
Molecular formula
C15H13NO5S
CAS number
57091-55-1
IUPAC name
[acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate
State
State

At room temperature, [acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate is typically in a solid form. It is stable under standard conditions and maintains its crystalline structure without sublimation or significant vapor pressure at room temperature.

Melting point (Celsius)
165.00
Melting point (Kelvin)
438.15
Boiling point (Celsius)
385.00
Boiling point (Kelvin)
658.15
General information
Molecular weight
379.42g/mol
Molar mass
379.4190g/mol
Density
1.2900g/cm3
Appearence

[Acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate typically appears as a yellow crystalline solid. The crystals are usually well-defined, which is common for many organic sulfate esters, and this gives it a characteristic appearance under natural or artificial light.

Comment on solubility

Solubility of [acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate

[acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate, a fascinating compound, showcases a varied profile in terms of solubility due to its unique molecular structure.

Solubility Characteristics:

  • Polar vs. Nonpolar: This compound contains both polar and nonpolar regions, leading to its solubility in various solvents.
  • Water Solubility: The presence of the hydrogen sulfate group generally enhances solubility in polar solvents like water, but the aromatic fluorenyl component may introduce some resistance to complete solubilization.
  • Solvent Compatibility: It is likely to be soluble in solvents such as:
    • Alcohols (e.g., methanol, ethanol)
    • Aqueous solutions that can stabilize its ionic forms

In summary, the solubility of [acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate is ultimately influenced by:

  1. Its ionic nature from the hydrogen sulfate group.
  2. The hydrophobic characteristics of the fluorenyl moiety.
  3. Environmental conditions such as temperature and pH.

As a result, the solubility behavior can be complex and may require empirical testing for precise characterization. Understanding the solubility of this compound is essential for applications in chemical synthesis and pharmaceutical formulation.

Interesting facts

Interesting Facts about [acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate

[acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate is a captivating compound with numerous intriguing aspects that highlight its significance in the field of chemistry.

Chemical Structure and Characteristics

  • Functional Groups: This compound contains an acetyl group and a sulfonate group, which contribute to its unique behavior and reactivity.
  • Amine Interaction: The presence of an amino group enhances the ability of this compound to participate in hydrogen bonding, making it relevant in various chemical reactions.
  • Fluorenyl Core: The fluorenyl structure allows for interesting *π-stacking interactions*, which can influence its stability and interactions with other molecules.

Applications and Uses

This compound is particularly valuable in:

  • Organic Synthesis: It plays a role in various synthetic pathways, including the preparation of other bioactive compounds.
  • Pharmaceutical Chemistry: The unique structural features make it a target for drug design, contributing potentially to medicinal chemistry.
  • Material Science: Given its intriguing molecular structure, it may find applications in the development of advanced materials, such as polymers or nanocomposites.

Research Significance

Scientists have recognized that compounds like [acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate can:

  • Enhance Reactivity: Its functional groups can be tailored to improve the efficiency of certain reactions, making it a subject of interest in mechanistic studies.
  • Exhibit Biological Activity: Research indicates potential antimicrobial properties linked to structural derivatives of this compound.

In conclusion, [acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate serves as a fascinating example of how structural features in chemistry can lead to diverse applications and influence ongoing research across multiple disciplines.

Synonyms
2-Acetylaminofluorene-N-sulfate
2-Acetylaminofluorene N-sulfate
N-(Sulfoxy)-2-fluorenylacetamide
16808-85-8
N-Sulfonyloxy-2-acetylaminofluorene
2-AAF-N-S
N-sulfooxy-2-acetylaminofluorene
DTXSID80168475
N-(sulfooxy)-2-fluorenylacetamide
N-sulfonoxy-2-AAF
N-(sulfooxy)-2-FAA
DTXCID0090966
Acetyl-9H-fluoren-2-ylazanyl hydrogen sulfate
2-acetamidofluorene N-sulfate
[acetyl(9H-fluoren-2-yl)amino] hydrogen sulfate
N-Sulfonoxy-aaf
N-(9H-fluoren-2-yl)-N-(sulfooxy)acetamide
N-(9H-fluoren-2-yl)-N-acetylhydroxylamine-O-sulfonic acid
Acetylaminofluorene-N-sulfate
N-Sulfonoxy-N-acetyl-2-aminofluorene
Sulfate ester of N-hydroxy-N-2-fluorenylacetamide
N-Fluoren-2-ylacetohydroxamic acid sulfate
Acetamide, N-9H-fluoren-2-yl-N-(sulfooxy)-
Hydroxylamine-O-sulfonic acid, N-acetyl-N-(2-fluorenyl)-
CHEBI:35424
ACETOHYDROXAMIC ACID, N-FLUOREN-2-YL-, SULFATE ESTER
NS00115921
Q27116473