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3,4-Dimethoxyacetophenone

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Identification
Molecular formula
C10H12O3
CAS number
1131-62-0
IUPAC name
1-(3,4-dimethoxyphenyl)ethanone
State
State
3,4-Dimethoxyacetophenone is typically found in a solid crystalline state at room temperature.
Melting point (Celsius)
38.00
Melting point (Kelvin)
311.15
Boiling point (Celsius)
293.00
Boiling point (Kelvin)
566.15
General information
Molecular weight
180.20g/mol
Molar mass
180.2030g/mol
Density
1.0832g/cm3
Appearence

3,4-Dimethoxyacetophenone appears as a white to slightly yellow solid. It is crystalline in nature and is often described as having a pleasant floral or sweet odor.

Comment on solubility

Solubility of 1-(3,4-dimethoxyphenyl)ethanone

1-(3,4-dimethoxyphenyl)ethanone is an organic compound that exhibits varying degrees of solubility depending on the solvent used. When examining its solubility, several key factors come into play:

  • Polarity: This compound features both hydrophobic and hydrophilic characteristics due to the presence of methoxy groups, which can influence its solubility in different environments.
  • Solvent Interaction: 1-(3,4-dimethoxyphenyl)ethanone is generally soluble in organic solvents such as alcohols and ethers. However, it demonstrates limited solubility in polar solvents like water.
  • Temperature Effects: Increased temperature often enhances solubility, which is particularly notable in this compound's interactions with organic solvents.

As a result, 1-(3,4-dimethoxyphenyl)ethanone may be described as:

  • Moderately soluble in ethanol and methanol.
  • Poorly soluble in water.

In summary, understanding the solubility of 1-(3,4-dimethoxyphenyl)ethanone is crucial for its practical applications in various chemical processes, especially in organic synthesis and pharmaceutical formulations.

Interesting facts

Interesting Facts about 1-(3,4-Dimethoxyphenyl)ethanone

1-(3,4-Dimethoxyphenyl)ethanone, often referred to in the scientific community for its intriguing structural features, is a notable compound in organic chemistry. This molecule serves as a bridge between simple carbonyl compounds and more complex aromatic systems, highlighting the diverse reactivity within organic frameworks.

Key Highlights:

  • Structural Versatility: The presence of both the ethyl and aromatic groups makes this compound a fascinating study in reactivity and interaction with other chemical species.
  • Applications: This compound has been investigated in the field of medicinal chemistry due to its potential biological activity and could serve as a template for the development of pharmaceuticals.
  • Synthetic Routes: It can be synthesized through various methods, such as Friedel-Crafts acylation, which adds value to its functionalization and application in synthetic chemistry.
  • Research Scope: Ongoing research focuses on its role in materials science and organic synthesis, where it can act as an intermediate or a building block for constructing more complex molecules.

As a chemistry student, one might appreciate the compound’s subtle variations and their implications:

  • This compound's dimethoxy groups offer an interesting look into electron-donating effects, which can influence reaction pathways.
  • The aromatic system not only provides stability but also participates in various substitution reactions, making it a significant subject for study in reaction mechanisms.

In the words of a noted organic chemist, "Understanding the unique properties of compounds like 1-(3,4-dimethoxyphenyl)ethanone is crucial to unlocking the secrets of organic synthesis."

This compound is an excellent example of how even simple molecules can have profound impacts in the realms of chemistry and medicine, making it a worthy subject for both academic and practical exploration.

Synonyms
1131-62-0
3',4'-Dimethoxyacetophenone
1-(3,4-Dimethoxyphenyl)ethanone
3,4-DIMETHOXYACETOPHENONE
Acetoveratrone
Ethanone, 1-(3,4-dimethoxyphenyl)-
3,4-Dimethoxyphenyl methyl ketone
1-(3,4-Dimethoxyphenyl)ethan-1-one
Acetophenone, 3',4'-dimethoxy-
4-Acetylveratrole
NSC 18708
5RV6436S8A
EINECS 214-468-0
3,4-dimethoxyphenylacetal
NSC 16944
NSC-16944
NSC-18708
AI3-11163
DTXSID4061549
CHEBI:86576
1-(4,5-DIMETHOXYPHENYL)ETHANONE
DTXCID2033316
Acetophenone, 3',4'-dimethoxy-(8CI)
MFCD00008737
Acetophenone,4'-dimethoxy-
Ethanone,4-dimethoxyphenyl)-
UNII-5RV6436S8A
bmse010033
3, 4-dimethoxyacetophenone
3,4-dimethoxy acetophenone
SCHEMBL76834
3',4'-dimethyoxyacetophenone
3,'-4'-Dimethoxyacetophenone
CHEMBL4218890
1-(3,4-dimethoxyphenyl)-ethanone
NSC16944
NSC18708
STR01828
3?,4?-DIMETHOXYACETOPHENONE
1-(3,4-Dimethoxy-phenyl)-ethanone
1-(3,4-Dimethoxyphenyl)ethanone #
3',4'-Dimethoxyacetophenone, 98%
AC7907
STK399977
1-(3,4-dimethoxyphenyl)-1-ethanone
AKOS000120461
CS-W005151
GF-0115
3',4'-Dimethoxyacetophenone, >=98%
AC-15467
SY015105
DB-041153
D1878
NS00010736
EN300-16176
3',4'-Dimethoxyacetophenone, analytical standard
4'-Hydroxy-3'-methoxyacetophenone, methyl ether
AQ-917/40710349
Q222993
Z54182939
F0191-0032
3 inverted exclamation mark ,4 inverted exclamation mark -Dimethoxyacetophenone