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Ethyl 2-(4-chlorophenyl)azo-3-oxobutanoate

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Identification
Molecular formula
C12H11ClN2O3
CAS number
2838-74-0
IUPAC name
ethyl 2-(4-chlorophenyl)azo-3-oxo-butanoate
State
State

At room temperature, ethyl 2-(4-chlorophenyl)azo-3-oxobutanoate is typically in a solid state. It is often a crystalline solid due to its organic nature and molecular structure.

Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
282.68g/mol
Molar mass
282.7100g/mol
Density
1.2903g/cm3
Appearence

Ethyl 2-(4-chlorophenyl)azo-3-oxobutanoate typically appears as a colored solid. The specific coloration can vary depending on the purity and specific conditions but azo compounds are often known for their vivid colors due to the presence of the azo group (-N=N-).

Comment on solubility

Solubility of Ethyl 2-(4-chlorophenyl)azo-3-oxo-butanoate

Ethyl 2-(4-chlorophenyl)azo-3-oxo-butanoate is a compound that showcases interesting solubility characteristics due to its chemical structure. Understanding the solubility of this compound can be essential for its applications in various fields such as pharmaceuticals and dyes.

In general, the solubility of a compound like ethyl 2-(4-chlorophenyl)azo-3-oxo-butanoate can be influenced by several factors:

  • Polarity: The presence of polar functional groups such as the ester functionality can make this compound more soluble in polar solvents.
  • Hydrophobicity: The aromatic ring from the 4-chlorophenyl group adds hydrophobic characteristics, which can lead to lower solubility in water but higher solubility in organic solvents.
  • Temperature: As with many organic compounds, increasing the temperature can enhance solubility in various solvents.
  • Concentration: At higher concentrations, solubility may be affected due to possible intermolecular interactions that could lead to precipitation.

In terms of practical applications, this compound is likely to be more soluble in organic solvents such as ethanol, acetone, and dichloromethane, which can facilitate its use in synthesis and formulation processes.

Ultimately, while specific solubility data might be limited, the nature of ethyl 2-(4-chlorophenyl)azo-3-oxo-butanoate suggests an affinity for organic solvents, making it crucial to consider these factors when working with this compound.

Interesting facts

Interesting Facts about Ethyl 2-(4-Chlorophenyl)azo-3-oxo-butanoate

Ethyl 2-(4-chlorophenyl)azo-3-oxo-butanoate is a fascinating compound belonging to the azo compound family. Azo compounds are characterized by the presence of the functional group -N=N-, which is responsible for their vibrant colors. Here are some notable aspects of this compound:

  • Color Change: Azo compounds are often known for their striking dyes. This property is not only aesthetically pleasing but also applicable in various industries, particularly textiles and food.
  • Biological Activity: Research indicates that compounds like ethyl 2-(4-chlorophenyl)azo-3-oxo-butanoate can exhibit significant biological activity, making them subjects of interest in medicinal chemistry.
  • Synthetic Pathways: The synthesis of this compound involves a multi-step process that highlights the creativity required in organic synthesis. Understanding its synthesis helps chemists grasp broader synthetic techniques.
  • Applications: Beyond its application as a dye, this azo compound may also find use in the creation of pharmaceuticals, agrochemicals, and other fine chemicals.

Furthermore, the presence of the 4-chlorophenyl group can influence the compound's reactivity and interaction with biological systems, making it a rich subject for study in both organic chemistry and pharmaceutical contexts. As you explore the properties and implications of ethyl 2-(4-chlorophenyl)azo-3-oxo-butanoate, consider how its structure correlates with its diverse applications and potential impacts in various fields!

Synonyms
2-((p-Chlorophenyl)azo)-3-oxobutyric acid ethyl ester
5869-60-3
BRN 0960967
4-Chlor-phenyl-azo-acetessigester [German]
4-Chlor-phenyl-azo-acetessigester
Butanoic acid, 2-((4-chlorophenyl)azo)-3-oxo-, ethyl ester
ACETOACETIC ACID, 2-((p-CHLOROPHENYL)AZO)-, ETHYL ESTER
SCHEMBL11767203
PXAXDTSHPSUWIP-UHFFFAOYSA-N
DTXSID201222285
2-(4'-chlorophenylazo)-acetoacetic acid ethyl ester
ethyl 2-[2-(4-chlorophenyl)diazenyl]-3-oxobutanoate