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4-Methylbenzaldehyde oxime

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Identification
Molecular formula
C8H9NO
CAS number
5468-37-1
IUPAC name
4-methylbenzaldehyde oxime
State
State

At room temperature, 4-methylbenzaldehyde oxime is in a solid state.

Melting point (Celsius)
75.00
Melting point (Kelvin)
348.15
Boiling point (Celsius)
292.00
Boiling point (Kelvin)
565.15
General information
Molecular weight
135.18g/mol
Molar mass
135.1760g/mol
Density
1.0610g/cm3
Appearence

4-Methylbenzaldehyde oxime appears as a white to pale yellow crystalline solid.

Comment on solubility

Solubility of 4-methylbenzaldehyde oxime

4-methylbenzaldehyde oxime, with the chemical formula C8H9NO, exhibits interesting solubility characteristics that can be influenced by various factors. Generally, this compound is known to be:

  • Soluble in organic solvents: 4-methylbenzaldehyde oxime dissolves well in organic solvents such as ethanol, acetone, and ether.
  • Limited solubility in water: Due to its hydrophobic aromatic structure and moderate polarity from the oxime functional group, its solubility in water is relatively low.

Understanding solubility is crucial, as it affects reactivity and applications in various fields. Some important points to consider include:

  • The presence of polar functional groups can enhance solubility in polar solvents.
  • Hydrogen bonding interactions significantly influence solubility in both organic and aqueous environments.

Ultimately, while 4-methylbenzaldehyde oxime shows suitable characteristics for organic solubility, its low aqueous solubility may limit its utility in specific applications where water solubility is essential. As a general rule, like dissolves like: polar solvents are better for polar solutes, while non-polar solvents work best for non-polar compounds. Understanding the solubility of this compound aids in its effective utilization in syntheses and other chemical processes.

Interesting facts

Interesting Facts about 4-methylbenzaldehyde oxime

4-methylbenzaldehyde oxime, an intriguing organic compound, is part of the oxime family, which are generally derived from aldehydes or ketones. This particular compound is notable for its unique structure and potential applications:

  • Synthesis: It is commonly synthesized through the reaction of 4-methylbenzaldehyde with hydroxylamine. This transformation highlights the versatility of carbonyl compounds in organic synthesis.
  • Functional Group: The presence of the oxime functional group (-C=N-OH) creates interesting chemical and physical properties, making it useful in various synthetic reactions.
  • Applications: 4-methylbenzaldehyde oxime shows promise in creating various pharmaceuticals and agrochemicals. It serves as an intermediate in the production of other chemical compounds.
  • Research Interest: The compound has attracted attention in environmental chemistry due to potential applications in toxin degradation and remediation.

As a potential future biopesticide, its derivatives could lead to sustainable agricultural practices. In the words of chemist Robert H. Grubbs, "Life is composed of a series of small, subtle changes." This statement rings true in the evolving research surrounding compounds like 4-methylbenzaldehyde oxime.

In summary, the significance of 4-methylbenzaldehyde oxime goes beyond its simple structure. Its capacity for various applications and its role in ongoing research pave the way for future innovations in chemistry.

Synonyms
p-Tolualdoxime
p-methylbenzaldehyde oxime
4-Methylbenzaldehyde oxime #
3717-15-5
MFCD01235928
4-methyl benzaldoxime
(alphaE)-N-Hydroxy-4-methylbenzenemethaneimine
SCHEMBL10603278
(hydroxyimino)(4-methylphenyl)methane
AKOS017263823
SY133551