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Cloxacillin Sodium

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Identification
Molecular formula
C19H17ClN3NaO5S
CAS number
7081-44-9
IUPAC name
sodium;6-[[3-(2-chlorophenyl)-5-methyl-isothiazole-4-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate
State
State

Cloxacillin sodium is typically found in a solid state at room temperature, specifically as a crystalline powder.

Melting point (Celsius)
194.00
Melting point (Kelvin)
467.15
Boiling point (Celsius)
-1.00
Boiling point (Kelvin)
-1.00
General information
Molecular weight
476.95g/mol
Molar mass
476.9450g/mol
Density
1.3300g/cm3
Appearence

Cloxacillin sodium appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of Sodium 6-[[3-(2-chlorophenyl)-5-methyl-isothiazole-4-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate

The solubility of this compound can be influenced by a variety of factors, including its molecular structure and the presence of functional groups. Here are some key points regarding its solubility:

  • Polarity: As a compound containing both hydrophilic (water-attracting) and hydrophobic (water-repelling) components, its solubility in water may be limited. The presence of the isothiazole and carboxylate functional groups can enhance solubility in polar solvents.
  • PH Levels: The solubility can change with pH; for instance, in acidic or basic environments, the ionization state of the carboxylate group can affect dissolution.
  • Temperature: Increased temperature generally increases the solubility of organic compounds; therefore, heating could potentially facilitate the dissolution process.
  • Solvent Compatibility: The solubility might vary significantly between organic solvents and aqueous solutions, with certain organic solvents potentially solubilizing the compound more effectively than water.

In conclusion, while the specific solubility data for this compound may require empirical testing, understanding these factors can provide valuable insights into how it may behave in different environments. As the adage goes, "Like dissolves like"—knowing the properties of various solvents will guide effective solubility assessments.

Interesting facts

Interesting Facts about Sodium 6-[[3-(2-chlorophenyl)-5-methyl-isothiazole-4-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate

The compound Sodium 6-[[3-(2-chlorophenyl)-5-methyl-isothiazole-4-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate is a fascinating example of a complex molecular structure that ties together several intriguing elements of organic chemistry. Here are some key points to note:

  • Unique Molecular Framework: The compound features a bicyclic structure that is characteristic of numerous natural products and pharmaceuticals. This unique configuration can lead to interesting biological activities.
  • Role of Isothiazole: The presence of the isothiazole ring in the compound suggests potential for antimicrobial and antifungal activity, which makes it a compound of interest in medicinal chemistry.
  • Chlorophenyl Group: The 2-chlorophenyl substituent adds intriguing properties to the molecule, possibly enhancing its solubility and reactivity. Such halogenated aromatic compounds are often linked to pharmaceuticals.
  • Applications: Compounds of this type may be investigated for their effectiveness in treating various diseases. The incorporation of specialized groups points towards its potential as a breakthrough drug.
  • Complexity: The intricate arrangement of atoms and functional groups reflects the challenges and excitement found in organic synthesis, as chemists strive to design and create such multifaceted molecules.

In summary, the Sodium 6-[[3-(2-chlorophenyl)-5-methyl-isothiazole-4-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate represents a compelling area of study within the realm of pharmaceuticals and synthetic chemistry. Its unique features provide valuable insights into the design of new compounds with enhanced biological activities.