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Fenoxanil

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Identification
Molecular formula
C13H7F3N2O5
CAS number
116143-79-8
IUPAC name
2-nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl)benzene
State
State

At room temperature, Fenoxanil is a solid.

Melting point (Celsius)
114.00
Melting point (Kelvin)
387.15
Boiling point (Celsius)
467.90
Boiling point (Kelvin)
741.05
General information
Molecular weight
368.21g/mol
Molar mass
368.2070g/mol
Density
1.4960g/cm3
Appearence

Fenoxanil appears as a pale yellow solid.

Comment on solubility

Solubility of 2-nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl)benzene

When considering the solubility of 2-nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl)benzene, various factors come into play, primarily influenced by its structural characteristics. This compound, which features both nitro and trifluoromethyl groups, exhibits certain properties that impact its interaction with solvents.

Key Factors Affecting Solubility:

  • Polarity: The presence of electron-withdrawing groups like the nitro and trifluoromethyl groups generally increases the polarity of the molecule, which can enhance its solubility in polar solvents.
  • Hydrophobic Regions: The aromatic rings contribute to hydrophobic characteristics, which may limit solubility in aqueous environments but can enhance solubility in organic solvents.
  • Steric Hindrance: The spatial arrangement of the substituents can affect how well the molecule fits in the solvent cage, potentially impacting solubility.

This compound has shown limited solubility in water due to its overall hydrophobic character, coupled with its tendency to aggregate. However, it is more soluble in organic solvents such as ethyl acetate and dimethyl sulfoxide (DMSO), making it favorable for applications within non-aqueous systems.

In summary, the solubility of 2-nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl)benzene emphasizes an intricate balance between its functional groups and solvent properties. Understanding this can aid in optimizing its use in various chemical applications.

Interesting facts

Interesting Facts about 2-Nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl)benzene

2-Nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl)benzene, often referred to as a complex organic compound, presents intriguing characteristics and applications in various fields of chemistry and technology. Here are some key highlights:

  • Structural Complexity: This compound features a unique structural arrangement, which includes both nitro groups and a trifluoromethyl substituent. Such structural diversity often contributes to interesting chemical reactivity and potential applications in synthetic pathways.
  • Electronics and Pharmaceuticals: Compounds with trifluoromethyl groups, like this one, are known for their role in enhancing the bioactivity of pharmaceutical agents. They are commonly found in agrochemicals and pharmaceuticals due to their ability to influence the electronic properties of the overall molecule.
  • Research Significance: Research has shown that compounds like these can act as precursors in the synthesis of more complex molecules, making them invaluable in drug discovery and materials science. The nitro groups can also serve as useful handles for further chemical modifications.
  • Environmental Impact: Given the presence of nitro and trifluoromethyl groups, understanding the degradation and environmental behavior of this compound is critical. Their stability can lead to accumulation in the environment if not properly managed.
  • Analytical Techniques: 2-Nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl)benzene can be analyzed using various spectroscopy techniques, which provide insights into its molecular interactions and behavior under different conditions.

In summary, this compound encapsulates the fascinating interplay between structure, reactivity, and applications in organic chemistry. Its intricate features make it a subject of interest for both researchers and students alike, further emphasizing the importance of studying diverse chemical entities.

Synonyms
Fluorodifen
15457-05-3
Preforan
Fluorodiphen
2-Nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl)benzene
Benzene, 2-nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl)-
p-Nitrophenyl 2-nitro-4-(trifluoromethyl)phenyl ether
4-Nitrophenyl 4-(trifluoromethyl)-2-nitrophenyl ether
C-6989
H4154A0WOP
DTXSID7037553
NSC-58415
DTXCID5017553
4-Nitrophenyl alpha,alpha,alpha-trifluoro-2-nitro-p-tolyl ether
p-Nitrophenyl alpha,alpha,alpha-trifluoro-2-nitro-p-tolyl ether
239-474-0
Soyex
Fluorodifene
Caswell No. 462AA
Fluordifen
2,4-Dinitro-p-trifluoromethyl phenyl ether
4-Trifluoromethyl-2,4'-dinitrophenyl ether
NSC 58415
C 6989
Ether, 2,4'-dinitro-4-trifluoromethyldiphenyl
p-Nitrophenyl 2-nitro-4-(trifluoromethyl) phenyl ether
CHEBI:5116
2,4'-Dinitro-4-(trifluoromethyl)diphenyl ether
Fluorodifen 100 microg/mL in Toluene
2-Nitro-1-(4-nitrophenoxy)-4-(trifluoromethyl) benzene
Ether, p-nitrophenyl .alpha.,.alpha.,.alpha.-trifluoro-2-nitro-p-tolyl
4-Trifluoromethyl-2,4'-dinitrodiphenyl ether
Fluorodifen [BSI:ISO]
4-Nitrophenyl .alpha.,.alpha.,.alpha.-trifluoro-2-nitro-p-tolyl ether
p-Nitrophenyl .alpha.,.alpha.,.alpha.-trifluoro-2-nitro-p-tolyl ether
Fluorodifene [ISO-French]
EINECS 239-474-0
EPA Pesticide Chemical Code 085001
BRN 2018474
UNII-H4154A0WOP
2,4'-Dinitro-4-trifluoromethyl-diphenyl ether
4-(Trifluoromethyl)-2,4'-dinitrodiphenyl ether
FLUORODIFEN [ISO]
NCIOpen2_007883
SCHEMBL39283
WLN: WNR DOR BNW BXFFF
CHEMBL1892429
SCHEMBL29419116
MSK22243
NSC58415
Tox21_301354
Ether, (p-nitrophenyl) (alpha,alpha,alpha-trifluoro-2-nitro-p-tolyl)
AKOS015903714
NCGC00163842-01
NCGC00255525-01
Ether,4'-dinitro-4-trifluoromethyldiphenyl
CAS-15457-05-3
C6989
CS-0891177
NS00010482
C 6929
Fluorodifen, PESTANAL(R), analytical standard
Ether,.alpha.,.alpha.-trifluoro-2-nitro-p-tolyl
Ether,.alpha.,.alpha.-trifluoro-2-nitro-p-tolyl)
2,4'-DINITRO-4-TRIFLUOROMETHYLDIPHENYL ETHER
4'-TRIFLUOROMETHYL-2',4-DINITRODIPHENYL ETHER
Q15809890
2,4'-DINITRO-4-(TRIFLUOROMETHYL) DIPHENYL ETHER
4-Nitrophenyl 2-nitro-4-(trifluoromethyl)phenyl ether #
4-nitrophenyl 4-(trifluoro methyl)-2-nitrophenyl ether
p-Nitrophenyl .alpha.,.alpha.-trifluoro-2-nitro-p-tolyl ether
3-NITRO-4-(P-NITROPHENOXY)-.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUOROTOLUENE
P-NITROPHENYL .ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-O-NITRO-P-TOLYL ETHER