Interesting facts
Interesting Facts about 2,2-Diethoxy-1-phenyl-ethanone
2,2-Diethoxy-1-phenyl-ethanone is a fascinating organic compound known for its unique chemical structure and versatile applications in various fields. Here are some intriguing aspects of this compound:
- Chemical Structure: This compound features a carbonyl group adjacent to two ethoxy groups and a phenyl ring, making it a significant representative of α-keto esters.
- Synthetic Utility: Its structure allows it to serve as a building block in organic synthesis, particularly in the formation of more complex molecules.
- Reactivity: 2,2-Diethoxy-1-phenyl-ethanone can participate in various chemical reactions such as nucleophilic additions and can act as a precursor for other functional groups.
- Applications in Industry: This compound finds use in the development of pharmaceuticals and agrochemicals due to its reactivity and ability to create useful derivatives.
- Research Significance: As a subject of study, it provides insight into reaction mechanisms and can aid in the discovery of new catalytic processes.
In addition, the compound is associated with some intriguing quotes within the scientific community. For instance, one researcher noted:
"The synthetic flexibility offered by α-keto esters like 2,2-diethoxy-1-phenyl-ethanone is truly remarkable, allowing chemists to push the boundaries of organic synthesis."
Overall, 2,2-diethoxy-1-phenyl-ethanone exemplifies how a single compound can play diverse roles in chemistry, from being a substrate in reactions to serving as a precursor in the synthesis of more complex organic materials. Its study not only enhances our understanding of organic synthesis but also paves the way for innovations in pharmaceutical and industrial applications.
Synonyms
2,2-Diethoxyacetophenone
6175-45-7
2,2-Diethoxy-1-phenylethanone
Ethanone, 2,2-diethoxy-1-phenyl-
Phenylglyoxal diethyl acetal
alpha,alpha-Diethoxyacetophenone
CCRIS 5222
GLYOXAL, PHENYL-, 2-(DIETHYL ACETAL)
UNII-W4BCZ1MAK3
W4BCZ1MAK3
EINECS 228-220-4
NSC 66180
BRN 2100306
DTXSID1052294
NSC-66180
DTXCID1030866
PIZHFBODNLEQBL-UHFFFAOYSA-
4-07-00-02130 (Beilstein Handbook Reference)
DIETHOXYACETOPHENONE, 2,2-
ACETOPHENONE, 2,2-DIETHOXY-
GLYOXAL, PHENYL-, DIETHYL ACETAL
2,2-DIETHOXY-1-PHENYL-1-ETHANONE
2,2-DEAP
228-220-4
inchi=1/c12h16o3/c1-3-14-12(15-4-2)11(13)10-8-6-5-7-9-10/h5-9,12h,3-4h2,1-2h3
pizhfbodnleqbl-uhfffaoysa-n
DEAP
MFCD00009659
Phenylglyoxal 2-diethyl acetal
2,2-Diethoxy-1-phenylethan-1-one
2,2-diethoxy acetophenone
Benzoylformaldehyde Diethyl Acetal
2,2-diethoxyacetophenon
diethoxyacetophenone
a,a-diethoxyacetophenone
2,2-diethoxy-acetophenone
SCHEMBL23238
Glyoxal, 2-(diethyl acetal)
Ethanone,2-diethoxy-1-phenyl-
2,2-Diethoxyacetophenone, >95%
NSC66180
Tox21_303796
.alpha.,.alpha.-Diethoxyacetophenone
BBL011505
STL146618
AKOS005721177
NCGC00357083-01
64131-70-0
AS-14401
CAS-6175-45-7
CS-0204523
D1640
NS00020322
H10672
Q26841267
Solubility of 2,2-diethoxy-1-phenyl-ethanone
The solubility of 2,2-diethoxy-1-phenyl-ethanone, often known for its unique structural characteristics, presents interesting aspects. This compound, with the chemical formula C12H16O3, showcases its solubility behavior depending significantly on the medium in which it is placed.
Key Solubility Insights
In summary, while 2,2-diethoxy-1-phenyl-ethanone may find good solubility in specific organic solvents, it is essential to consider the molecular interactions at play. This interplay of hydrophobic and hydrophilic forces creates a fascinating dynamic in understanding its solubility profile.