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4-Methoxybenzophenone

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Identification
Molecular formula
C14H12O2
CAS number
611-94-9
IUPAC name
(4-methoxyphenyl)-(p-tolyl)methanone
State
State

This compound is typically found in a solid state at room temperature.

Melting point (Celsius)
59.00
Melting point (Kelvin)
332.15
Boiling point (Celsius)
347.00
Boiling point (Kelvin)
620.15
General information
Molecular weight
226.27g/mol
Molar mass
226.2740g/mol
Density
1.1440g/cm3
Appearence

4-Methoxybenzophenone is a pale yellow solid. It typically appears as crystalline powder.

Comment on solubility

Solubility of (4-methoxyphenyl)-(p-tolyl)methanone

The solubility of (4-methoxyphenyl)-(p-tolyl)methanone can be influenced by several factors related to its chemical structure. This compound features aromatic rings, which generally play a significant role in its solubility profile.

Factors Affecting Solubility

  • Polarity: The presence of the methoxy group increases the polarity of the molecule, which can enhance solubility in polar solvents such as alcohols.
  • Hydrogen Bonding: The ability of the methoxy group to form hydrogen bonds may facilitate solubility in polar solvents.
  • Aromatic Nature: The aromatic rings may lead to limited solubility in water due to their hydrophobic characteristics.

In summary, the solubility of (4-methoxyphenyl)-(p-tolyl)methanone can be characterized as follows:

  1. It is likely soluble in organic solvents like ethanol and acetone.
  2. Its solubility in water is expected to be limited due to the hydrophobic nature of the aromatic components.

As a general observation, the solubility of aromatic compounds tends to vary significantly based on their molecular structure, so factors such as temperature and the specific solvent employed can also greatly influence the results.

Interesting facts

Interesting Facts About (4-methoxyphenyl)-(p-tolyl)methanone

(4-methoxyphenyl)-(p-tolyl)methanone, often referred to as a derivative of ketones, belongs to a fascinating class of compounds that have garnered significant attention in both synthetic and medicinal chemistry. Here are some notable facts about this intriguing compound:

  • Functional Groups: The presence of a methoxy group and a phenyl group contributes to the compound's reactivity and ability to form various derivatives, making it a versatile building block in organic synthesis.
  • Reactivity: Ketones, such as this compound, are known for their ability to undergo nucleophilic addition reactions. This characteristic opens up avenues for various chemical transformations essential in organic synthesis.
  • Pharmaceutical Relevance: Compounds containing methoxy and aromatic ring systems frequently exhibit biological activity. Researchers are exploring their potential use in developing pharmaceutical agents due to their unique structural features.
  • Synthetic Pathways: The synthesis of (4-methoxyphenyl)-(p-tolyl)methanone typically involves Friedel-Crafts acylation, showcasing how established reactions can be tailored to produce complex molecules efficiently.
  • Research Potential: Ongoing studies are delving into the compound's applications in materials science, particularly in creating functional materials that can be used in electronics and photonics.

As a student or scientist, exploring (4-methoxyphenyl)-(p-tolyl)methanone can deepen your understanding of ketonic compounds and their roles in both nature and industry. Whether it's for synthesizing new materials or developing innovative drugs, this compound is a reminder of the *infinite possibilities* that lie within organic chemistry.

Synonyms
(4-methoxyphenyl)(4-methylphenyl)methanone
RefChem:402952
839-795-1
23886-71-7
4-Methoxy-4'-methylbenzophenone
(4-Methoxyphenyl)(p-tolyl)methanone
(4-methoxyphenyl)-(4-methylphenyl)methanone
MFCD00025812
BENZOPHENONE, 4-METHOXY-4'-METHYL-
(4-Methoxy-phenyl)-p-tolyl-methanone
NSC 163357
BRN 2049977
NSC163357
SCHEMBL758577
4-methyl-4'methoxybenzophenone
DTXSID50178586
HMS1607H06
YAA88671
STK285988
(4-methoxyphenyl)-(p-tolyl)methanone
AKOS001482630
HS-3167
NSC-163357
Benzophenone, 4-methoxy-4//'-methyl-
4-methoxyphenyl-4-methylphenyl methanone
NCGC00338263-01
DB-046283
CS-0251178
EN300-53905
G27596
AB01331605-02
886M717
AK-918/40897229
SR-01000392949
SR-01000392949-1
Z276846040