Interesting facts
Interesting Facts about 1-(1-naphthyl)ethanone
1-(1-naphthyl)ethanone, often referred to as an aryl ketone, is a fascinating compound due to its chemical structure and diverse applications. Here are some intriguing aspects of this compound:
- Chemical Structure: This compound consists of a naphthalene ring system attached to an ethanone group, giving it a unique aromatic character and the ability to participate in various chemical reactions.
- Reactivity: The presence of the carbonyl group (C=O) allows for reactivity towards nucleophiles, making it a pivotal compound in organic synthesis. It can undergo nucleophilic addition reactions and can also be transformed into other functional groups.
- Applications: 1-(1-naphthyl)ethanone serves as a critical intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its derivatives often exhibit interesting biological activities.
- Spectroscopy Significance: Due to its distinct structure, it provides challenging yet rewarding insights using techniques like NMR spectroscopy, where the unique hydrogen environments can yield rich spectra.
- Photoactive Properties: This compound can also exhibit photochemical behavior, making it valuable in the study of photoredox chemistry, an essential area in developing new materials and solar energy applications.
- Historical Context: Compounds similar to 1-(1-naphthyl)ethanone have been studied for over a century and have significantly contributed to the field of organic synthesis and mechanistic studies.
In conclusion, 1-(1-naphthyl)ethanone not only showcases intriguing chemical properties but also emphasizes the versatility of aromatic ketones in synthetic chemistry. Its multifaceted roles highlight the ongoing importance of studying and utilizing such compounds in various scientific fields.
Synonyms
1'-Acetonaphthone
941-98-0
1-Acetylnaphthalene
1-Acetonaphthone
1-Acetonaphthalene
Ethanone, 1-(1-naphthalenyl)-
1-(1-Naphthalenyl)ethanone
1-Naphthyl methyl ketone
alpha-Acetonaphthone
alpha-Acetylnaphthalene
alpha-Naphthyl methyl ketone
1-(1-Naphthyl)ethanone
Methyl alpha-naphthyl ketone
NSC 7659
Ethanone, 1-(naphthalenyl)-
EINECS 213-384-1
BRN 1100618
U44R403XVS
AI3-00673
NSC-7659
LIQUID U-80
alpha-Methyl naphthyl ketone
DTXSID4052635
4-07-00-01292 (Beilstein Handbook Reference)
1-ACETONAPHTHONE [INCI]
DTXCID1031208
213-384-1
inchi=1/c12h10o/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-8h,1h
Methyl 1-naphthyl ketone
1-(naphthalen-1-yl)ethanone
1-naphthalen-1-ylethanone
1-(naphthalen-1-yl)ethan-1-one
1`-Acetonaphthone
MFCD00004013
.alpha.-Acetonaphthone
.alpha.-Acetylnaphthalene
1-naphthalen-1-yl-ethanone
.alpha.-Naphthyl methyl ketone
Methyl .alpha.-naphthyl ketone
UNII-U44R403XVS
1-Acetonaphtone
Acetyl naphthalene
methylnaphthylketone
1\'-Acetonaphthone
1'-Acetylnaphthalene
1-Acetonaphthone, 97%
1-(1-Naphthyl)ethanone #
SCHEMBL50651
ghl.PD_Mitscher_leg0.724
1-(naphthalen-4-yl)ethanone
.alpha.-Methyl naphthyl ketone
Monomethylnaphthalene Formaldehyde
NSC7659
HY-I0717
STR04053
STL183335
1-Acetonaphthone, analytical standard
AKOS000118730
CS-W020048
FS-3189
SY013630
DB-287152
A0052
A1044
NS00012937
EN300-19188
D70015
Q27290663
F0001-2262
Z104473080
Solubility of 1-(1-naphthyl)ethanone
1-(1-naphthyl)ethanone, also known as α-naphthylacetone, exhibits unique solubility characteristics influenced by its molecular structure. This compound is primarily considered to be soluble in organic solvents, making it particularly useful in various chemical applications. Here are some key points regarding its solubility:
To summarize, the solubility of 1-(1-naphthyl)ethanone can be best described as:
These solubility properties are essential for chemists when selecting solvents for synthesis and extraction processes involving 1-(1-naphthyl)ethanone.