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(6-oxo-1H-pyridazin-3-yl) 3,4-dichlorobenzoate

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Identification
Molecular formula
C11H5Cl2N2O3
CAS number
38985-64-1
IUPAC name
(6-oxo-1H-pyridazin-3-yl) 3,4-dichlorobenzoate
State
State

At room temperature, this compound exists as a solid substance, specifically forming a crystalline powder. The presence of chlorine atoms contributes to the stability and solid state of the compound.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
285.07g/mol
Molar mass
285.1050g/mol
Density
1.6000g/cm3
Appearence

The compound appears as a yellow crystalline powder. Its structure is composed of a dichlorobenzoate moiety linked to a pyridazinone group, resulting in an aromatic and polar molecule.

Comment on solubility

Solubility of (6-oxo-1H-pyridazin-3-yl) 3,4-dichlorobenzoate

The solubility of (6-oxo-1H-pyridazin-3-yl) 3,4-dichlorobenzoate in various solvents can be quite interesting due to its structural characteristics. While specific quantitative solubility data may not be readily available, several factors can be considered when discussing its solubility:

  • Polarity: The presence of chlorine atoms in the aromatic ring can influence the overall polarity of the compound. Compounds with higher polarity tend to be more soluble in polar solvents such as water or alcohols.
  • Hydrogen Bonding: The functional groups involved may allow for hydrogen bonding interactions, which can enhance solubility in certain solvents.
  • Solvent Compatibility: Like many organic compounds, this derivative may be more soluble in organic solvents such as ethanol, dichloromethane, or acetone, rather than in aqueous environments.
  • Temperature Influence: Solubility can also increase with temperature; therefore, conducting solubility tests at varying temperatures could yield different results.

In summary: predicting the solubility of (6-oxo-1H-pyridazin-3-yl) 3,4-dichlorobenzoate requires a thorough understanding of its chemical structure and interactions with different solvents. Further empirical studies will definitely elucidate its behavior in solution.

Interesting facts

Interesting Facts about (6-oxo-1H-pyridazin-3-yl) 3,4-dichlorobenzoate

The compound (6-oxo-1H-pyridazin-3-yl) 3,4-dichlorobenzoate is a fascinating member of the pyridazine family, known for its distinctive structure and various applications in fields such as pharmaceuticals and agrochemicals. Here are some intriguing insights about this compound:

  • Structural Significance: The presence of both pyridazine and benzoate moieties in its structure allows for unique reactivity and interaction patterns that are not commonly found in similar compounds.
  • Biological Activity: Compounds like (6-oxo-1H-pyridazin-3-yl) 3,4-dichlorobenzoate showcase promising biological activities. Research has indicated that derivatives of such structures may exhibit anti-inflammatory and analgesic properties.
  • Potential Applications: Due to its unique structure, this compound has potential utility in the synthesis of new pharmaceutical agents. It is also being studied for its possible role in designing agrochemicals that target specific pests with minimal environmental impact.
  • Modern Synthesis Techniques: Chemists continue to innovate new synthetic pathways for obtaining compound structures like this one, employing methods such as microwave-assisted synthesis and one-pot reactions to enhance efficiency and yield.
  • Research and Development: The ongoing research surrounding pyridazine derivatives highlights the compound's potential as a template for developing new molecules with enhanced biological activities. As noted in the literature, "The exploration of heterocyclic compounds opens new avenues in medicinal chemistry."

In summary, the compound (6-oxo-1H-pyridazin-3-yl) 3,4-dichlorobenzoate is more than just a chemical entity; it embodies the intersection of modern chemistry, potential medicinal applications, and innovative synthesis techniques. Its continued study could lead to significant advancements in various scientific fields.

Synonyms
BRN 0813542
13386-09-9
BENZOIC ACID, 3,4-DICHLORO-, 2,3-DIHYDRO-3-OXO-6-PYRIDAZINYL ESTER
2,3-Dihydro-3-oxo-6-pyridazinyl 3,4-dichlorobenzoate
3,4-Dichlorobenzoic acid 2,3-dihydro-3-oxo-6-pyridazinyl ester
DTXSID90158403
5-25-01-00057 (Beilstein Handbook Reference)
DTXCID8080894