Interesting facts
Interesting Facts about 1-phenylbutane-1,3-dione
1-phenylbutane-1,3-dione, often referred to as a fluoroacetone derivative, is an intriguing organic compound that has garnered interest due to its versatile applications in various fields. Here are some notable aspects:
- Structure & Functionality: This compound features a unique diketone structure, characterized by two carbonyl groups. This structure enables it to participate in numerous chemical reactions, particularly in organic synthesis.
- Biological Activity: 1-phenylbutane-1,3-dione has been studied for its potential biological activities. Some research suggests it may exhibit antimicrobial properties, which could be essential in the development of new pharmaceutical agents.
- Synthetic Applications: The compound serves as an effective building block in organic synthesis. It can be used to create complex molecules, making it a valuable asset in both academic and industrial laboratories.
- Historical Significance: Compounds like 1-phenylbutane-1,3-dione have emerged in many pivotal studies in the field of organic chemistry. Research surrounding diketones has fostered advancements in understanding reaction mechanisms and catalysis.
- Experimental Insights: Chemists often utilize 1-phenylbutane-1,3-dione to explore reaction conditions, such as temperature and catalyst choice, to study their effects on product formation. This makes it not only a useful compound but also a tool for educational purposes.
In summary, the fascinating properties and applications of 1-phenylbutane-1,3-dione make it a compound worth examining in both academic and practical chemistry settings. As research continues to uncover its potential, this diketone will likely remain a subject of interest.
Synonyms
Benzoylacetone
93-91-4
1-Phenylbutane-1,3-dione
1-PHENYL-1,3-BUTANEDIONE
1-Benzoylacetone
1,3-Butanedione, 1-phenyl-
Acetoacetophenone
Acetylbenzoylmethane
1-Benzoyl-2-propanone
2-Propanone, benzoyl-
Benzoyl-aceton
2-Acetylacetophenone
benzoyl acetone
1-phenyl-butane-1,3-dione
Benzoyl-aceton [German]
MFCD00008786
.alpha.-Acetylacetophenone
NSC 4015
AI3-10572
EINECS 202-286-4
UNII-I3RUV8U115
BRN 0742413
DTXSID3021803
NSC-4015
1-phenylbutan-1,3-dione
NSC-100655
DTXCID901803
I3RUV8U115
4-PHENYL-2,4-BUTANEDIONE
4-07-00-02151 (Beilstein Handbook Reference)
4-OXO-4-PHENYLBUTAN-2-ONE
NSC-83580
NSC-83581
NSC-87898
NSC-88942
NSC-97232
NSC-97233
PHENYL-1,3-BUTANEDIONE, 1-
NSC-404283
NSC-405722
NSC-405723
NSC-405724
1-METHYL-3-PHENYL-1,3-PROPANEDIONE
alpha-Acetylacetophenone
1-phenyl-1,3-butandione
benzoylaceton
1Benzoylacetone
acetyl acetophenone
1Benzoyl2propanone
2Acetylacetophenone
2Propanone, benzoyl
alphaAcetylacetophenone
1Phenyl1,3butanedione
1Phenylbutane1,3dione
1,3Butanedione, 1phenyl
1-phenyl-butane-1,3 dione
SCHEMBL15116
CHEMBL3186793
NSC4015
1-Phenyl-1,3-butanedione, 99%
STR01075
Tox21_202879
NSC100655
STK802149
AKOS000119529
CS-W014323
FB00886
HY-W013607
PS-3611
CAS-93-91-4
NCGC00260425-01
SY011141
DB-013671
NS00022887
EN300-19842
1-Phenyl-1,3-butanedione, purum, >=98.0% (GC)
Q27280358
F3098-2657
Solubility of 1-phenylbutane-1,3-dione
1-phenylbutane-1,3-dione, with its intriguing structure, exhibits interesting solubility characteristics that are mostly influenced by its molecular composition. Here are some key points regarding its solubility:
In summary, 1-phenylbutane-1,3-dione is soluble in polar organic solvents but shows limited solubility in water, reflecting the classic behavior of many organic compounds. As with many such substances, understanding its solubility can be crucial for applications in synthesis and formulation.