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N-(4-nitrophenyl)benzohydrazonoyl bromide

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Identification
Molecular formula
C13H10BrN3O2
CAS number
34976-76-8
IUPAC name
N-(4-nitrophenyl)benzohydrazonoyl bromide
State
State

At room temperature, N-(4-nitrophenyl)benzohydrazonoyl bromide is typically found in a solid state.

Melting point (Celsius)
156.00
Melting point (Kelvin)
429.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
334.15g/mol
Molar mass
334.1490g/mol
Density
1.6490g/cm3
Appearence

N-(4-nitrophenyl)benzohydrazonoyl bromide appears as a crystalline solid powder. It is typically yellow to orange in color, depending on purity and precise formulation.

Comment on solubility

Solubility of N-(4-nitrophenyl)benzohydrazonoyl bromide

N-(4-nitrophenyl)benzohydrazonoyl bromide is a compound that exhibits intriguing solubility characteristics. Understanding its solubility behavior requires considering several factors:

  • Polarity: The presence of both a nitrophenyl group and a hydrazonoyl moiety in its structure can create a polar environment, which may limit its solubility in non-polar solvents.
  • Solvent Interaction: This compound is likely to have increased solubility in polar organic solvents, such as dimethyl sulfoxide (DMSO) and methanol, due to the polar functional groups that can interact favorably with the solvent molecules.
  • Temperature Dependence: Solubility can also be influenced by temperature; generally, higher temperatures can enhance the solubility of solid compounds in liquids.

The solubility of N-(4-nitrophenyl)benzohydrazonoyl bromide is not just a matter of "dissolve or not dissolve." It involves a complex interplay of molecular interactions. As solvated molecules come together, the degree of solubility reflects the balance between enthalpic and entropic factors:

  1. Enthalpy: The energy change associated with breaking intermolecular attractions when dissolving.
  2. Entropy: The degree of disorder that is introduced into the system when the compound dissolves.

In summary, N-(4-nitrophenyl)benzohydrazonoyl bromide's solubility is largely dependent on the surrounding environment and solvent choice, making it a fascinating subject for study in the field of chemical solubility.

Interesting facts

Interesting Facts about N-(4-nitrophenyl)benzohydrazonoyl bromide

N-(4-nitrophenyl)benzohydrazonoyl bromide is a remarkable compound that straddles the fascinating interface between organic chemistry and materials science. Here are some intriguing aspects that make this compound noteworthy:

  • Versatile Applications: This compound finds diverse applications in organic synthesis, particularly as an intermediate in the production of various pharmaceuticals and agrochemicals.
  • Chromophoric Properties: The nitrophenyl group imparts unique electronic properties, resulting in distinct chromophoric behavior, which can be leveraged in dye and pigment formulations.
  • Reactivity: The bromide moiety serves as an excellent leaving group, facilitating nucleophilic substitutions, thus making it a valuable reagent in many synthetic pathways.
  • Research Significance: Ongoing studies involving this compound help in understanding reaction mechanisms and the design of new materials with tailored properties for specific applications.

Quote from a Chemist: "The beauty of compounds like N-(4-nitrophenyl)benzohydrazonoyl bromide lies not only in their structural elegance but also in their potential to unlock new scientific frontiers in both synthesis and application."

In summary, the unique structure and functional groups of N-(4-nitrophenyl)benzohydrazonoyl bromide make it a compound of interest not only in academia but also in various industries. Its versatility and reactivity ensure it remains a topic of discussion and research within the realm of chemical sciences.

Synonyms
962-13-0
N-(4-Nitrophenyl)benzenecarbohydrazonoyl bromide
DTXSID201240493
amino-[bromo(phenyl)methylene]-(4-nitrophenyl)ammonium