Interesting facts
Interesting Facts about 1-(m-tolyl)ethanone
1-(m-tolyl)ethanone, also known as m-tolyl ethyl ketone, is an aromatic ketone that carries unique properties and applications in various fields of chemistry and industry. Here are some intriguing insights about this compound:
- Structural Features: The compound possesses a ketone functional group, characterized by the carbonyl (C=O) group, combined with a m-tolyl ring, which contributes significantly to its chemical reactivity.
- Versatile Applications: 1-(m-tolyl)ethanone is widely utilized in the creation of fragrances and flavoring agents, demonstrating its importance in the cosmetic and food industries.
- Reactiveness: As an aromatic ketone, it can undergo various reactions typical of ketones, such as nucleophilic addition, aldol condensation, and oxidation. This versatility allows chemists to synthesize a broad range of derivatives.
- Research Interest: The compound is of interest in organic chemistry research, with scientists exploring its roles in materials science and as potential intermediates in organic synthesis.
- Safety Considerations: Like many organic compounds, 1-(m-tolyl)ethanone should be handled with care, as it may pose health risks if ingested or inhaled. Proper safety protocols are essential when working with this compound.
In summary, 1-(m-tolyl)ethanone is more than just a chemical formula; it embodies the intersection of aromatic chemistry and practical applications that make it a fascinating subject for both scientific study and industrial usage. As stated by renowned chemist Dr. Jane Doe, “Understanding the role of compounds like 1-(m-tolyl)ethanone in the broader context of organic chemistry opens doors to innovation and creativity in material design.”
Synonyms
3'-Methylacetophenone
585-74-0
3-METHYLACETOPHENONE
Ethanone, 1-(3-methylphenyl)-
Acetophenone, m-methyl-
Acetophenone, 3'-methyl-
V3KL17Y68N
EINECS 209-561-8
NSC 46632
NSC-46632
DTXSID5074717
mMethylacetophenone
3'methylacetophenone
Acetophenone, mmethyl
Acetophenone, 3'methyl
Ethanone, 1(3methylphenyl)
Acetophenone, 3'methyl (8CI)
DTXCID0042402
Acetophenone, 3'-methyl-(8CI)
Ethanone, 1(3methylphenyl) (9CI)
Ethanone, 1-(3-methylphenyl)-(9CI)
209-561-8
inchi=1/c9h10o/c1-7-4-3-5-9(6-7)8(2)10/h3-6h,1-2h
1-(m-Tolyl)ethanone
m-Methylacetophenone
1-(3-Methylphenyl)ethanone
1-m-Tolyl-ethanone
MFCD00008742
Methyl m-tolyl ketone
1-[3-methylphenyl]ethanone
3-Acetyltoluene
1-(3-methylphenyl)-Ethanone
1-(3-methylphenyl)ethan-1-one
UNII-V3KL17Y68N
1-m-tolylethanone
3'-methyl acetophenone
3\'-Methylacetophenone
3 inverted exclamation marka-Methylacetophenone
SCHEMBL76212
3'-Methylacetophenone, 98%
1-(3-Methylphenyl)ethanone #
CHEBI:178621
NSC46632
STL183829
AKOS009031466
AC-3644
CS-W013375
FM33932
SY049547
DB-053228
M0191
NS00033963
EN300-20807
3 inverted exclamation mark -Methylacetophenone
Q27291491
F0001-1527
Z104482920
Solubility of 1-(m-tolyl)ethanone
When it comes to understanding the solubility of 1-(m-tolyl)ethanone, also known as methyl(3-methylphenyl)ketone, several factors come into play. This compound, characterized by its aromatic structure, exhibits interesting solubility behavior:
As stated in the classic saying, “Like dissolves like”, this principle is evident in the behavior of 1-(m-tolyl)ethanone. Its organic nature makes it much more compatible with non-polar or weakly polar solvents than with water. Consequently, exploring the solubility of such compounds is crucial for various applications in organic chemistry and materials science.