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N-(4-nitrophenyl)benzohydrazonoyl chloride

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Identification
Molecular formula
C13H9ClN3O2
CAS number
69154-30-1
IUPAC name
N-(4-nitrophenyl)benzohydrazonoyl chloride
State
State
The compound is in a solid state at room temperature.
Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
377.15
Boiling point (Kelvin)
650.30
General information
Molecular weight
274.67g/mol
Molar mass
274.6610g/mol
Density
1.4360g/cm3
Appearence

The compound appears as an orange to red-brown crystalline powder.

Comment on solubility

Solubility of N-(4-nitrophenyl)benzohydrazonoyl chloride

N-(4-nitrophenyl)benzohydrazonoyl chloride is a unique compound that exhibits interesting solubility characteristics, primarily influenced by its chemical structure. Solubility can be a critical factor in various applications, including synthesis and extraction processes. Here are some key points regarding the solubility of this compound:

  • Solvent Compatibility: This compound is generally soluble in organic solvents such as acetone, dichloromethane, and ethyl acetate, which are often used in chemical reactions and extractions.
  • Water Solubility: N-(4-nitrophenyl)benzohydrazonoyl chloride is likely to have limited solubility in water, owing to its hydrophobic aromatic rings.
  • Influence of Temperature: Like many organic compounds, its solubility may increase with temperature, allowing for better dissolution in appropriate solvents when heated.
  • Reaction with Water: It is important to note that exposure to water may lead to hydrolysis, affecting its integrity and utility.

Understanding the solubility of N-(4-nitrophenyl)benzohydrazonoyl chloride is essential for optimizing its usage in different chemical processes. As always, it is advisable to perform solubility tests in specific solvent systems to confirm behavior under experimental conditions.

Interesting facts

Exploring N-(4-nitrophenyl)benzohydrazonoyl chloride

N-(4-nitrophenyl)benzohydrazonoyl chloride is a fascinating compound that holds significance in various fields of chemistry, especially in synthetic organic chemistry. Here are some intriguing aspects of this compound:

  • Diverse Applications: This compound is commonly used as a reagent in the synthesis of complex organic molecules. Its ability to act as an electrophile makes it a valuable tool for building more intricate structures in pharmaceutical intermediates and agrochemical products.
  • Nitrophenyl Moiety: The presence of the 4-nitrophenyl group contributes to its reactivity. The nitro group is an excellent electron-withdrawing group, which enhances the compound's electrophilic nature, allowing it to participate in a variety of chemical reactions.
  • Chemical Transformation: As an acyl chloride, it is reactive with various nucleophiles such as alcohols and amines, leading to the formation of amides or esters, which are essential functional groups in organic chemistry.
  • Research and Exploration: Scientists often explore the derivatives and reaction pathways of N-(4-nitrophenyl)benzohydrazonoyl chloride to discover new synthetic methodologies and develop novel materials with unique properties.
  • Safety Considerations: Working with this compound does necessitate caution due to its reactivity and potential hazards. Proper lab safety protocols must be followed to handle this compound safely during experiments.

In conclusion, N-(4-nitrophenyl)benzohydrazonoyl chloride is more than just a chemical entity; it's a gateway to expanding organic synthesis. As researchers delve deeper into its properties and reactions, they unlock new possibilities for innovation in chemistry.

Synonyms
N-(4-Nitrophenyl)benzenecarbohydrazonoyl chloride
DTXSID301231124
benzoyl chloride 4-nitrophenyl-hydrazone