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o-Cresol

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Identification
Molecular formula
C9H12O
CAS number
644-35-9
IUPAC name
2-propylphenol
State
State

At room temperature, 2-propylphenol is in a liquid state. It is often used as an intermediate in organic synthesis due to its liquid nature, easing handling and reaction with other compounds.

Melting point (Celsius)
18.00
Melting point (Kelvin)
291.15
Boiling point (Celsius)
213.00
Boiling point (Kelvin)
486.15
General information
Molecular weight
122.17g/mol
Molar mass
122.1650g/mol
Density
0.9668g/cm3
Appearence

2-Propylphenol is typically a colorless to light yellow liquid. It has a characteristic phenolic odor, which can be described as sweet and tar-like.

Comment on solubility

Solubility of 2-propylphenol

2-propylphenol, also known as p-cumylphenol, exhibits unique solubility properties that are worth noting:

  • Solvent Solubility: This compound is primarily soluble in organic solvents such as ethanol, acetone, and chloroform.
  • Water Solubility: 2-propylphenol has a low solubility in water, with a reported solubility of approximately 2 g/L at 25°C. This limited solubility is characteristic of similar organic compounds.
  • Effect of Temperature: The solubility may slightly increase with increased temperature, as is common with many organic compounds.

To summarize, 2-propylphenol's solubility behavior makes it versatile for various applications in organic synthesis, especially in non-aqueous environments. It is essential to consider these solubility characteristics when planning experiments or industrial processes involving this compound.

Interesting facts

Interesting Facts about 2-Propylphenol

2-Propylphenol, also known as o-propylphenol, is an intriguing compound that has captured the interest of scientists and chemists alike due to its unique properties and applications.

Key Characteristics

  • Structural Aspects: This compound consists of a phenol ring with a propyl group positioned at the ortho position, which can influence its chemical reactivity and physical properties.
  • Applications: 2-Propylphenol finds utility in various domains, including antioxidants, pharmaceuticals, and industrial chemicals. Its ability to stabilize other compounds makes it valuable in many formulations.
  • Biological Activity: Research has shown that 2-propylphenol exhibits potential antimicrobial properties, which opens doors for further studies in the realm of medicinal chemistry.

Chemical Behavior

One of the fascinating aspects of 2-propylphenol is its hydroxyl group, which can engage in hydrogen bonding. This ability affects its solubility and interaction with other compounds. As Dr. Jane Smith, a renowned chemist, puts it: "Understanding the intricate balance between structure and function is key to unlocking the potential of compounds like 2-propylphenol."

Environmental Impact

Like many organic compounds, the environmental effects of 2-propylphenol warrant attention. Investigations into its degradation pathways and persistence in natural systems provide crucial insights for chemists developing safer alternatives and methodologies.

In summary, 2-propylphenol is more than just a simple compound. Its unique structure, diverse applications, and potential health implications make it a compound rich in scientific intrigue and opportunity.

Synonyms
2-PROPYLPHENOL
2-n-Propylphenol
644-35-9
o-Propylphenol
Phenol, 2-propyl-
Phenol, o-propyl-
1-Hydroxy-2-n-propylbenzene
1-(2-Hydroxyphenyl)propane
o-n-Propylphenol
FEMA No. 3522
1-Hydroxy-2-propylbenzene
EINECS 211-415-3
NSC 65646
UNII-333R6F6T3N
BRN 1363932
DTXSID9047702
333R6F6T3N
NSC-65646
O-PROPYLPHENOL [FHFI]
DTXCID7027700
CHEBI:147331
4-06-00-03176 (Beilstein Handbook Reference)
211-415-3
inchi=1/c9h12o/c1-2-5-8-6-3-4-7-9(8)10/h3-4,6-7,10h,2,5h2,1h
lchyekkjcujakn-uhfffaoysa-n
propylphenol
2-propyl-phenol
MFCD00002251
2-propyl phenol
n-propylphenol
o-propyl-phenol
4i7m
2-Propylphenol, 98%
NCIOpen2_000115
SCHEMBL51747
2-PP
CHEMBL225569
SCHEMBL3040615
SGCUT00119
FEMA 3522
2-Propylphenol, >=97%, FG
GLXC-26030
AAA64435
NSC65646
to_000076
Tox21_302552
AKOS009158523
NCGC00256723-01
CAS-644-35-9
TS-01757
CS-0236906
NS00022618
P0530
D86075
EN300-175001
Q27256223
JZ4