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Disperse Yellow 54

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Identification
Molecular formula
C27H34N2O3
CAS number
12223-55-7
IUPAC name
2,7-bis[2-(diethylamino)ethoxy]fluoren-9-one
State
State

At room temperature, Disperse Yellow 54 is in a solid state. It is stable under normal conditions and is widely used in its solid form for various applications.

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.15
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.15
General information
Molecular weight
436.58g/mol
Molar mass
436.5810g/mol
Density
1.2200g/cm3
Appearence

Disperse Yellow 54 typically appears as a yellow crystalline powder. It is notable for its vibrant yellow color, which is utilized mainly in the textile industry for dyeing purposes.

Comment on solubility

Solubility of 2,7-bis[2-(diethylamino)ethoxy]fluoren-9-one

The compound 2,7-bis[2-(diethylamino)ethoxy]fluoren-9-one (C27H34N2O3) exhibits notable solubility characteristics due to its unique molecular structure.

Factors Influencing Solubility

Understanding the solubility of this compound can be fixed on several important factors:

  • Molecular Structure: The presence of diethylamino groups enhances solubility in polar solvents.
  • Polarity: Characterized by both polar and non-polar regions, which enables solubility in a mixture of solvents.
  • Functional Groups: The ethoxy groups contribute to interactions with solvent molecules.

In Solvents

This compound is generally soluble in:

  • Organic solvents, such as chloroform and ethanol, due to its nonpolar hydrocarbon backbone.
  • Polar solvents, enabling moderate solubility in water under certain conditions.

Summary

In summary, the solubility of 2,7-bis[2-(diethylamino)ethoxy]fluoren-9-one can be characterized as:

  • Moderate to High in organic solvents.
  • Variable in aqueous environments depending on concentration and temperature.

In conclusion, the balance between hydrophilic and hydrophobic characteristics plays a crucial role in its solubility profile, making it a versatile compound in various chemical applications.

Interesting facts

Interesting Facts about 2,7-bis[2-(diethylamino)ethoxy]fluoren-9-one

2,7-bis[2-(diethylamino)ethoxy]fluoren-9-one is a fascinating chemical compound that has drawn significant interest in both academic and industrial settings. Here are some noteworthy points:

1. Fluorescent Properties

  • Fluorescent Dyes: This compound exhibits remarkable fluorescent properties, making it valuable in the development of fluorescent dyes used in various applications, including bioimaging and sensing technologies.
  • Organic Light Emitting Diodes (OLEDs): Its ability to emit light when excited makes it a potential candidate in OLED technology, which is pivotal for energy-efficient displays.

2. Unique Structure

  • Fluorenone Core: The compound features a fluorenone moiety, which is a central component that is recognized for its stability and diversified reactivity.
  • Substituents: The presence of diethylamino groups enhances its solubility and influences its electronic properties, making it versatile in different chemical environments.

3. Biological Activity

  • Potential Pharmacological Applications: Research indicates that compounds with similar structural frameworks may exhibit biological activity, suggesting potential uses in medicinal chemistry.
  • Study of Interactions: The diethylamino ethoxy substituents may provide insights into the interactions of compounds with biological systems, enhancing the understanding of drug design.

4. Syntheses and Modifications

  • Versatile Synthesis: The synthesis of this compound typically involves multi-step organic reactions, showcasing the creativity required in synthetic organic chemistry.
  • Modification Potential: The structure allows for further modifications, opening pathways for tailoring properties for specific applications.

As a compound that bridges various fields of chemistry, 2,7-bis[2-(diethylamino)ethoxy]fluoren-9-one serves as an excellent example of how chemical structure influences both functionality and application. Its unique properties make it an exciting subject of study for both chemists and researchers in related fields.

Synonyms
tilorone
27591-97-5
Bis-DEAE-fluorenone
Tilorona
9H-Fluoren-9-one, 2,7-bis[2-(diethylamino)ethoxy]-
Tilorone [INN]
Tiloronum
2,7-Bis-DEAE-fluorenone
Amixin IC
2,7-Bis(2-(diethylamino)ethoxy)-9H-fluoren-9-one
2,7-bis[2-(diethylamino)ethoxy]fluoren-9-one
O6W7VEW6KS
DTXSID1045958
9H-FLUOREN-9-ONE, 2,7-BIS(2-(DIETHYLAMINO)ETHOXY)-
2,7-bis[2-(diethylamino)ethoxy]-9H-fluoren-9-one
RMI 10008DA
NCGC00095196-01
DTXCID9025958
Tiloronum [INN-Latin]
Tilorona [INN-Spanish]
CAS-27591-97-5
NSC143969
UNII-O6W7VEW6KS
BRN 2011558
2,7-Bis(2-diethylaminoethoxy)fluoren-9-one dihydrochloride
Spectrum_000231
TILORONE [MI]
Spectrum2_001742
Spectrum3_001055
Spectrum5_001889
ChemDiv1_019101
2,7-bis(2-diethylaminoethyloxy)fluoren-9-one
TILORONE [WHO-DD]
2,7-Bis[2-(diethylamino)ethoxy]-9-fluorenone
Tiloron (*dihydrochloride*)
Oprea1_331997
BSPBio_002610
KBioSS_000711
Tilorone hydrochloride(USAN)
CHEMBL47298
DivK1c_000018
SCHEMBL352401
SPECTRUM2300009
SPBio_001844
HMS500A20
HMS641E05
HY-B1080A
KBio1_000018
KBio2_000711
KBio2_003279
KBio2_005847
KBio3_001830
CHEBI:109553
CHEBI:147347
MPMFCABZENCRHV-UHFFFAOYSA-N
NINDS_000018
HMS1922J22
HMS2094I17
Pharmakon1600-02300009
BCP34398
Tox21_111484
BDBM50364890
CCG-39449
NSC759311
RMI 10008DA (*dihydrochloride*)
STL483841
AKOS025310183
Tox21_111484_1
NSC-759311
IDI1_000018
Bis-DEAE-fluorenone (*dihydrochloride*)
NCGC00095196-02
NCGC00095196-03
NCGC00095196-04
NCGC00095196-06
NCGC00178576-01
AC-24571
AS-14877
SBI-0052826.P002
CS-0013836
G78315
AB00053319_02
SR-05000001961
Q2028068
SR-05000001961-1
BRD-K34568562-001-03-5
BRD-K34568562-001-04-3
BRD-K34568562-300-01-5
2, {7-Bis[2-(diethylamino)ethoxy]fluoren-9-one} dihydrochloride
2,7-Bis[2-(diethylamino)ethoxy]-9-fluorenone; Bis-DEAE-fluorenone
9H-Fluoren-9-one, {2,7-bis[2-(diethylamino)ethoxy]-,} dihydrochloride
Fluoren-9-one, 2, {7-bis[2-(diethylamino)ethoxy]-,} dihydrochloride