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3'-methoxyacetophenone

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Identification
Molecular formula
C9H10O2
CAS number
586-37-8
IUPAC name
1-(3-methoxyphenyl)ethanone
State
State

At room temperature, 3'-methoxyacetophenone is typically found in a crystalline solid state if purified, but it can also exist in a liquid form depending on the environmental conditions.

Melting point (Celsius)
32.00
Melting point (Kelvin)
305.15
Boiling point (Celsius)
248.00
Boiling point (Kelvin)
521.15
General information
Molecular weight
150.17g/mol
Molar mass
150.1740g/mol
Density
1.1000g/cm3
Appearence

3'-Methoxyacetophenone appears as a colorless to pale yellow liquid. It has a distinctive aromatic odor characteristic of ketones. This compound can be found as a crystalline solid when it is cooled or at lower temperatures.

Comment on solubility

Solubility of 1-(3-methoxyphenyl)ethanone

The compound 1-(3-methoxyphenyl)ethanone, with its distinctive structure, presents interesting solubility characteristics that depend significantly on its molecular interactions.

Its solubility can generally be described as follows:

  • Polar Solvents: It displays moderate solubility in polar solvents such as water. This is primarily due to the presence of the methoxy group, which can engage in hydrogen bonding.
  • Non-Polar Solvents: Conversely, it is more soluble in non-polar organic solvents such as hexane and benzene, as the larger aromatic components favor dispersion forces.
  • Temperature Dependence: Like many organic compounds, its solubility is also affected by temperature. Increased temperatures generally enhance solubility in both polar and non-polar solvents.
  • pH Influence: The solubility can be altered with changes in pH, particularly in aqueous solutions, where protonation states may affect interactions with solvent molecules.

In summary, the solubility of 1-(3-methoxyphenyl)ethanone is a complex interplay of its structural properties and the nature of the solvent. The combination of both polar and non-polar features in its structure allows it to adapt its solubility profile based on the surrounding environment. This compound serves as a fascinating example of how molecular design influences solubility characteristics.

Interesting facts

Interesting Facts About 1-(3-Methoxyphenyl)ethanone

1-(3-methoxyphenyl)ethanone, commonly known as a derivative of acetophenone, is a fascinating compound with several notable features:

  • Functional Groups: This compound contains both an ethanone (ketone) group and a methoxy-substituted aromatic ring, contributing to its interesting chemical reactivity.
  • Synthesis and Applications: It can be synthesized through Friedel-Crafts acylation, a method that highlights the importance of electrophilic aromatic substitution in organic chemistry.
  • Precursor in Organic Chemistry: Due to its structure, it serves as a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals.
  • Uses in Flavor and Fragrance: Its pleasant aromatic properties are utilized in producing flavoring agents and fragrances, making it popular in the food and cosmetic industries.
  • Biological Activity: Research suggests that compounds with similar structures may exhibit antimicrobial and antifungal properties, emphasizing the importance of studying such derivatives.

As a scientist, understanding the intricate details of 1-(3-methoxyphenyl)ethanone opens doors to exploring deeper chemical reactions and their potential applications in the real world. The combination of its unique functional groups makes it a compound of interest for both research and industrial applications.

Synonyms
3'-Methoxyacetophenone
586-37-8
3-Methoxyacetophenone
3-Acetylanisole
m-Methoxyacetophenone
1-(3-METHOXYPHENYL)ETHANONE
Ethanone, 1-(3-methoxyphenyl)-
Acetophenone, m-methoxy-
NSC 65593
Acetophenone, 3'-methoxy-
1K3UR56Z4N
EINECS 209-573-3
NSC-65593
AI3-26011
DTXSID10207321
RIVASTIGMINE HYDROGEN TARTRATE IMPURITY H [EP IMPURITY]
RIVASTIGMINE HYDROGEN TARTRATE IMPURITY H (EP IMPURITY)
mMethoxyacetophenone
3'Methoxyacetophenone
Acetophenone, mmethoxy
Acetophenone, 3'methoxy
Ethanone, 1(3methoxyphenyl)
Acetophenone, 3'methoxy (8CI)
DTXCID10129812
Acetophenone, 3'-methoxy-(8CI)
Ethanone, 1(3methoxyphenyl) (9CI)
Ethanone, 1-(3-methoxyphenyl)-(9CI)
209-573-3
1-(3-Methoxyphenyl)ethan-1-one
MFCD00008736
1-(3-methoxy-phenyl)-ethanone
meta-Methoxyacetophenone
m-Acetylanisole; m-Methoxyacetophenone
m-Acetanisole
3-METHOXYACETOPHENONE (D3)
1-Acetyl-3-methoxybenzene
UNII-1K3UR56Z4N
m-Acetylanisole
3-acetanisole
3-Acetoanisole
m-Metoxyacetophenone
m-Methoxy acetophenone
3-methoxy acetophenone
3?-Methoxyacetophenone
3/'-Methoxyacetophenone
3\'-Methoxyacetophenone
3-Methoxy-1-acetylbenzene
NCIOpen2_000067
SCHEMBL52445
Methyl 3-methoxyphenyl ketone
1-(3-methoxyphenyl)-ethanone
3'-Methoxyacetophenone, 97%
1-(3-Methoxyphenyl)ethanone #
CHEMBL5270199
SCHEMBL12015247
1-[3-(methyloxy)phenyl]ethanone
NSC65593
STK802448
AKOS000119490
CS-W020599
FM34460
PS-5287
AC-10020
SY003673
DB-028538
m-Acetylanisole;1-(3-Methoxyphenyl)ethanone
M0104
NS00020529
EN300-16173
3 inverted exclamation marka-Methoxyacetophenone
L10020
3 inverted exclamation mark -Methoxyacetophenone
Q27252520
Z54179675
F0001-1530
m-Acetanisole; m-Acetylanisole; m-Acetylanisole; m-Acetanisole
InChI=1/C9H10O2/c1-7(10)8-4-3-5-9(6-8)11-2/h3-6H,1-2H