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Acetyl(9H-fluoren-2-yl)amino acetate

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Identification
Molecular formula
C17H15NO3
CAS number
1140-89-4
IUPAC name
[acetyl(9H-fluoren-2-yl)amino] acetate
State
State
The compound is a solid at room temperature.
Melting point (Celsius)
146.00
Melting point (Kelvin)
419.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
285.29g/mol
Molar mass
285.2850g/mol
Density
1.3200g/cm3
Appearence

Acetyl(9H-fluoren-2-yl)amino acetate appears as a white to off-white crystalline powder. It has a characteristic aromatic odor. The compound is usually stable under standard conditions.

Comment on solubility

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

The solubility of [acetyl(9H-fluoren-2-yl)amino] acetate can be quite intriguing due to the unique structure of the compound. It is important to consider various factors that can influence its solubility:

  • Polarity: The presence of the acetyl group contributes to the overall polarity, which can enhance solubility in polar solvents.
  • Hydrogen Bonding: The amino group can form hydrogen bonds with solvents, potentially increasing solubility in water and alcohols.
  • Temperature: Like many organic compounds, solubility may increase with temperature, allowing for greater dissolution in various solvents.
  • pH Sensitivity: The compound's solubility might also vary with pH, depending on ionization of the amino group.

In general, compounds like [acetyl(9H-fluoren-2-yl)amino] acetate may exhibit better solubility in:

  • Polar solvents, such as water and methanol.
  • Organic solvents that can interact through dipole-dipole or hydrogen bonding.

Yet, it is critical to perform specific solubility tests to accurately determine how this compound behaves in different environments. Moreover, the structural complexity indicates that factors such as molecular interactions will play a significant role in determining solubility. As noted, “solubility is not just a characteristic; it is a phenomenon influenced by multiple intricate factors that govern the behavior of compounds in various states.”

Interesting facts

Exploring the Wonders of [acetyl(9H-fluoren-2-yl)amino] acetate

[acetyl(9H-fluoren-2-yl)amino] acetate is a remarkable compound that resides at the intersection of organic chemistry and material science. Its structure is derived from the fluorenyl platform, providing unique characteristics and functionalities that chemists find intriguing. Here are some interesting facts that highlight the significance of this compound:

  • Versatile Intermediates: This compound serves as an important intermediate in organic synthesis, particularly in the development of pharmaceuticals. Its ability to participate in various reactions makes it a valuable tool for chemists.
  • Fluorene Framework: The fluorenyl unit in its structure contributes to its photochemical and electronic properties, which have implications in fields such as organic electronics and photonics.
  • Synthetic Routes: The synthesis of [acetyl(9H-fluoren-2-yl)amino] acetate can involve various methodologies, including acylation reactions. Understanding these routes can enhance a chemist's repertoire of synthetic strategies.
  • Biological Activity: Compounds related to amino acetates typically exhibit interesting biological activities. Thus, deriving potential medicinal applications from this compound could spark new research avenues.
  • Research Context: Due to their unique properties, compounds like [acetyl(9H-fluoren-2-yl)amino] acetate are often studied in the context of developing new materials, including polymers and dyes.

This compound not only reflects the beauty of chemical synthesis but also underscores the intricate relationship between molecular structure and function. As a chemistry student or enthusiast, exploring the various applications and synthetic pathways of sources like [acetyl(9H-fluoren-2-yl)amino] acetate can deepen your appreciation for the field and inspire innovative ideas.

In the words of renowned chemist Jean-Pierre Sauvage, "Science is a fascinating adventure that leads to the quest for knowledge and understanding."

Engaging with compounds such as [acetyl(9H-fluoren-2-yl)amino] acetate showcases how chemistry can lead to significant advancements in technology and health.

Synonyms
Acetoxy AAF
ACETOXYACETYLAMINOFLUORENE
N-Acetoxy-2-acetamidofluorene
Acetoxyacetamidofluorene
N-Acetoxy-N-acetyl-2-aminofluorene
NA-AAF
N-Acetoxyacetylaminofluorene
CCRIS 729
2-(Acetoxyacetylamino)fluorene
CHEBI:76331
N-Acetoxy-N-acetyl-aminofluorene
N-Acetoxy-2-acetyl aminofluorene
BRN 2222410
DTXSID90209828
N-Acetyl-N-acetoxy-2-aminofluorene
N-acetyloxy-N-(9H-fluoren-2-yl)acetamide
Acetoxyfluorenylacetamide
N Acetoxy 2 acetylaminofluorene
N Acetoxy N acetyl 2 aminofluorene
DTXCID40132319
nfomhwalmfwnaq-uhfffaoysa-n
6098-44-8
N-Acetoxy-2-acetylaminofluorene
NAAAF
N-Acetoxy-2-fluorenylacetamide
N-Acetoxy-N-2-fluorenylacetamide
Acetamide, N-(acetyloxy)-N-9H-fluoren-2-yl-
N-(Fluoren-2-yl)acetohydroxamic acetate
2-Acetoxyacetylaminofluorene
N-Acetoxy-2-acetaminofluorene
N-(Fluoren-2-yl)acetohydroxamic acetamide
Acetic acid, ester with N-(fluoren-2-yl)acetohydroxamic acid
NSC 163627
Acetic acid, (N-acetyl-N-(2-fluorenyl)amino) ester
N-(Acetoxy)-N-9H-fluoren-2-ylacetamide
N-Acetoxy-N-(9H-fluoren-2-yl)acetamide
N-(Acetyloxy)-N-9H-fluoren-2-ylacetamide
Acetamide, N-(acetoxy)-N-9H-fluoren-2-yl-
Hydroxylamine, N,O-diacetyl-N-fluoren-2-yl-
Acetic acid, [N-acetyl-N-(2-fluorenyl)amino] ester
[acetyl(9H-fluoren-2-yl)amino] acetate
SCHEMBL73231
CHEMBL85327
GLXC-10389
NSC163627
NSC-163627
WLN: L B656 HHJ ENV1&OV1
Hydroxylamine,O-diacetyl-N-fluoren-2-yl-
Q4673285