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3-Nitrobiphenyl

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Identification
Molecular formula
C12H9NO2
CAS number
2113-58-8
IUPAC name
1-nitro-3-phenyl-benzene
State
State

At room temperature, 3-Nitrobiphenyl is in a solid state, often found in crystalline form.

Melting point (Celsius)
47.00
Melting point (Kelvin)
320.00
Boiling point (Celsius)
306.00
Boiling point (Kelvin)
579.00
General information
Molecular weight
199.21g/mol
Molar mass
199.2070g/mol
Density
1.2040g/cm3
Appearence

3-Nitrobiphenyl appears as a pale yellow crystalline solid. It lacks any distinct odor and can form well-defined crystals.

Comment on solubility

Solubility of 1-nitro-3-phenyl-benzene

1-nitro-3-phenyl-benzene, a nitro-substituted aromatic compound, presents interesting solubility characteristics predominantly influenced by its non-polar aromatic structure. In essence, the solubility of this compound can be summarized as follows:

  • Solvent Compatibility: 1-nitro-3-phenyl-benzene is generally more soluble in non-polar or slightly polar organic solvents, such as:
    • Hexane
    • Toluene
    • Chloroform
  • Water Solubility: This compound exhibits a very low solubility in water due to:
  • Hydrophobic Nature: The presence of the large phenyl groups creates a hydrophobic environment, making interactions with water molecules unfavorable.
  • Temperature Factors: Increased temperature may enhance solubility slightly in organic solvents but is not significant in water.

In summary, the solubility of 1-nitro-3-phenyl-benzene is primarily influenced by its structure and the nature of the solvents, emphasizing a preference for organic over aqueous environments. Understanding this aspect is pivotal when considering its applications and reactivity in various chemical processes.

Interesting facts

Interesting Facts about 1-Nitro-3-phenyl-benzene

1-Nitro-3-phenyl-benzene, often referred to by its IUPAC name, is a fascinating compound in the realm of organic chemistry. As a member of the nitroaromatic family, this compound exhibits unique properties and applications due to the presence of both nitro and phenyl functional groups.

Key Characteristics

  • Electrophilic Reactivity: The nitro group (-NO2) attached to the benzene ring significantly enhances its electrophilic character, making it a prime candidate for further chemical reactions.
  • Industrial Importance: Compounds like 1-nitro-3-phenyl-benzene serve as intermediates in the synthesis of dyes, pharmaceuticals, and agrochemicals. Their role in chemical manufacturing cannot be overstated.
  • Environmental Consideration: As with many nitro compounds, there are environmental and health concerns associated with their use and degradation. Studying these aspects is crucial for ensuring safety in applications.

Chemical Behavior

When exploring the chemical behavior of 1-nitro-3-phenyl-benzene, it is essential to note:

  • Its ability to undergo nucleophilic substitution reactions.
  • How the position of the nitro group influences the reactivity of the compound.
  • The potential for reduced derivatives to form, which can yield further interesting compounds.

Research Significance

This compound serves as a model for understanding:

  • Electrophilic aromatic substitution reactions.
  • Intermolecular interactions in complex organic systems.
  • Insights into the mechanisms of nitro group substitutions.

In summary, 1-nitro-3-phenyl-benzene is not just a simple organic compound; it is a gateway to deeper insights in organic chemistry, providing both challenges and opportunities for research and industrial applications. Its continued study can lead to advancements in synthetic methodologies and chemical safety practices.

Synonyms
3-Nitrobiphenyl
2113-58-8
1,1'-Biphenyl, 3-nitro-
3-Nitro-1,1'-biphenyl
Biphenyl, 3-nitro-
M-NITROBIPHENYL
EINECS 218-305-4
NSC 408697
BRN 1872195
DTXSID00175363
DTXCID7097854
1,1'-Biphenyl, 3-nitro-(9CI)
218-305-4
1-nitro-3-phenylbenzene
3-Nitrodiphenyl
3-nitro biphenyl
3'-Nitrobiphenyl
7UA7CEP6GJ
NSC-408697
1,1'-Biphenyl,3-nitro-
m-Nitrodiphenyl
MFCD00007245
NSC408697
3-Nitrobiphenyl, 99%
UNII-7UA7CEP6GJ
NITROBIPHENYL, M-
1-nitro-3-phenyl-benzene
3-PHENYLNITROBENZENE
Cambridge id 5108021
SCHEMBL2009026
FYRPEHRWMVMHQM-UHFFFAOYSA-
1,1'-Biphenyl, 3-nitro- (9CI)
AKOS015833363
GS-5407
DB-045493
CS-0206916
N0193
NS00026793
F13606
A815157
Q63393016
F0001-0754
InChI=1/C12H9NO2/c14-13(15)12-8-4-7-11(9-12)10-5-2-1-3-6-10/h1-9H