Interesting facts
Interesting Facts about 4-Phenylbutan-2-one
4-Phenylbutan-2-one, also known as ethyl phenylacetate, is a fascinating compound with a variety of applications and noteworthy characteristics. Here are some engaging insights:
- Synthesis: This compound can be synthesized through various methods, including the crossed aldol condensation reaction. This reaction underscores the importance of carbonyl chemistry in organic synthesis.
- Applications: 4-Phenylbutan-2-one is not just a chemical curiosity; it has applications in the flavor and fragrance industry. It can impart a sweet, fruity scent, making it valuable in perfumery and as a flavoring agent.
- Use in Research: Due to its reactivity and utility, this compound is often utilized in organic synthesis as a precursor for various chemical transformations, paving the way for the production of more complex molecules.
- Structural Features: The presence of the phenyl group in its structure contributes to its stability and reactivity, providing an excellent platform for further functionalization in synthetic pathways.
- Physiological Effects: Research into the physiological effects of 4-phenylbutan-2-one suggests that it may have a role in influencing the central nervous system, although more studies are needed to fully understand its impact.
In summary, 4-phenylbutan-2-one is a compound that bridges practical applications in everyday products with complex chemical behavior, representing the intersection of science and industry.
Synonyms
BENZYLACETONE
4-Phenylbutan-2-one
4-Phenyl-2-butanone
2-Butanone, 4-phenyl-
Benzyl acetone
UNII-UZM5QH16YW
UZM5QH16YW
EINECS 219-847-4
BRN 1907123
DTXSID6033241
AI3-15123
NSC-813
4-PHENYL BUTANONE
NSC-44829
DTXCID4013241
EC 219-847-4
4-07-00-00713 (Beilstein Handbook Reference)
1082501-60-7
1Phenyl3butanone
4Phenylbutan2one
2Butanone, 4phenyl
Methyl 2phenylethyl ketone
betaPhenylethyl methyl ketone
801-687-7
akggybadqzyzpd-uhfffaoysa-n
2550-26-7
4-Penylbutan-2-one
1-Phenyl-3-butanone
Methyl phenethyl ketone
Phenethyl methyl ketone
Methyl 2-phenylethyl ketone
4-Phenyl-butan-2-one
Methyl phenylethyl ketone
NSC 813
MFCD00008790
NSC 44829
2-Phenylethyl methyl ketone
beta-Phenylethyl methyl ketone
CAS-2550-26-7
4-phenylbutanone
1-phenylbutan-3-one
Methyl 2-phenethyl ketone
SCHEMBL1346
MLS001055395
4-Phenyl-2-butanone, 98%
NSC813
QSPL 147
CHEMBL1490851
.beta.-Phenylethyl methyl ketone
CHEBI:195507
HMS2270M10
NSC44829
Tox21_201240
Tox21_303341
BBL011439
s9376
STL146547
AKOS000119009
CCG-266189
CS-W016332
FP32146
HY-W015616
SB40570
NCGC00090923-01
NCGC00090923-02
NCGC00257254-01
NCGC00258792-01
4-Phenyl-2-butanone, analytical standard
AS-54099
DA-51037
SMR000112390
SY013502
B0405
NS00007656
EN300-19146
A25848
P17497
Q410405
F0001-0855
1-Phenyl-3-butanone;2-Butanone, 4-phenyl-;4-Phenyl-2-butanoine
Solubility of 4-phenylbutan-2-one
4-phenylbutan-2-one, a compound with the formula C10H12O, exhibits solubility characteristics that are quite intriguing and relevant in various chemical contexts. Due to its structural properties, this compound presents the following solubility behavior:
In summary, understanding the solubility of 4-phenylbutan-2-one is crucial for its application in synthetic chemistry and materials science, where solubility can dictate its usability in reactions and formulations.