Interesting facts
Interesting Facts about 1,2-Diphenylethane-1,2-dione
1,2-Diphenylethane-1,2-dione, commonly recognized in the field of organic chemistry for its unique structure and reactivity, is an intriguing compound. Here are some compelling points about this compound:
- Structural Significance: The compound features a symmetrical arrangement of phenyl groups bonded to a central dione group. This symmetrical structure plays a critical role in its chemical behavior and interactions.
- Reactivity: As a diketone, 1,2-diphenylethane-1,2-dione can undergo various chemical transformations, making it a valuable intermediate in synthetic organic chemistry.
- Applications: It serves as a precursor in the synthesis of several biologically active molecules and can also function as a ligand in coordination chemistry due to the presence of electron-withdrawing carbonyl groups.
- Significance in Research: The compound has been studied for its potential applications in medicinal chemistry, specifically for its contribution to the development of pharmaceuticals.
- Known Reactions: It is involved in various reactions such as nucleophilic addition and condensation, which are pivotal in the development of more complex organic molecules.
In summary, 1,2-diphenylethane-1,2-dione represents an essential building block in organic synthesis and research. Its intriguing properties and versatility in reactions make it a subject of continued study and interest within the chemical community.
Synonyms
BENZIL
134-81-6
Dibenzoyl
Diphenylethanedione
Diphenylglyoxal
1,2-Diphenylethane-1,2-dione
Bibenzoyl
Ethanedione, diphenyl-
1,2-Diphenylethanedione
diphenylethane-1,2-dione
Glyoxal, diphenyl-
Diphenyldiketon
1,2-ethanedione, 1,2-diphenyl-
Esacure KBO
Diphenyl-alpha,beta-diketone
Wy 20910
CCRIS 6179
NSC 220315
WY-20910
EINECS 205-157-0
MFCD00003080
UNII-S85X61172J
CHEBI:51507
AI3-00898
Diphenyl-.alpha.,.beta.-diketone
NSC-4041
NSC-220315
S85X61172J
Diphenylethanedione (Benzil)
CHEMBL189886
DTXSID3044380
1,2-diphenyl-ethane-1,2-dione
EC 205-157-0
1,2-dione
WLN: RVVR
diphenyl-alpha-beta-ketone
PHENYTOIN IMPURITY B (EP IMPURITY)
PHENYTOIN IMPURITY B [EP IMPURITY]
1,2-Diphenyl-1,2-ethanedione
PHENYTOIN SODIUM IMPURITY B (EP IMPURITY)
PHENYTOIN SODIUM IMPURITY B [EP IMPURITY]
Benzil, 98%
SCHEMBL66
BENZIL [MI]
Diphenylethanedione;Dibenzoyl
DTXCID1024380
BDBM22722
NSC4041
Benzil(Diphenylethane-1,2-Dione)
HMS3755K05
Tox21_302031
NSC220315
STL283960
AKOS000120196
FB34685
NCGC00255924-01
Benzil-Melting Point 94.90 degrees C
BS-15243
CAS-134-81-6
Benzil Zone Refined (number of passes:22)
B0050
B0221
Benzil - Melting Point 94.90 masculineC
CS-0012125
NS00004291
EN300-19182
Benzil (96 degrees C) Melting Point Standard
C20226
G81221
1,2-ETHANEDIONE,1,2-DIPHENYL BENZIL
AB-131/13435226
Q818497
F3096-2306
Z104473066
Benzil;Diphenylethanedione;Diphenylglyoxal;1,2-Diphenylethanedione;Dibenzoyl
103852-36-4
205-157-0
InChI=1/C14H10O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10
Solubility of 1,2-diphenylethane-1,2-dione
1,2-diphenylethane-1,2-dione, often referred to in the realm of organic chemistry, exhibits some distinct characteristics when it comes to its solubility. Here are some key points to consider:
Overall, it is noteworthy that 1,2-diphenylethane-1,2-dione's solubility profile predominantly favors non-polar solvents which reflects its molecular structure and interactions. As one researcher aptly stated, "Understanding the solubility can lead to greater insights into the reactivity and application of the compound."