Interesting facts
Interesting Facts About 2-Phenylindane-1,3-Dione
2-Phenylindane-1,3-dione is a fascinating organic compound that belongs to the class of diones, which are compounds containing two carbonyl groups. This compound is particularly interesting for several reasons:
- Versatile Applications: 2-Phenylindane-1,3-dione has been studied for its potential uses in pharmaceuticals and organic synthesis, making it a valuable compound for medicinal chemistry.
- Structure Significance: The structure features an indane ring fused with a phenyl group, which is essential for its chemical behavior and reactivity. This unique arrangement allows for various substitution reactions, enhancing its versatility.
- Analytical Chemistry: The detection and analysis of this compound can be performed using techniques like NMR (Nuclear Magnetic Resonance) and mass spectrometry. Such methods are invaluable for understanding its molecular structure and interactions.
- Synthetic Pathways: The synthesis of 2-phenylindane-1,3-dione often involves intricate reactions, showcasing how organic chemists can manipulate molecular structures to create desired compounds.
- Biological Activity: Some studies suggest that compounds structurally related to 2-phenylindane-1,3-dione exhibit biological activity, which could be beneficial in drug development. This opens avenues for further exploration in cancer research and other medical fields.
In summary, 2-phenylindane-1,3-dione embodies the intersection of synthetic organic chemistry and biological potential. The study of such compounds not only expands our understanding of organic reactions but also fuels innovations in therapeutic applications. As you delve deeper into the realm of organic chemistry, this compound serves as an enlightening case of how chemistry can lead to significant advancements.
Synonyms
phenindione
83-12-5
2-Phenyl-1,3-indandione
2-Phenyl-1H-indene-1,3(2H)-dione
Rectadione
Phenylindanedione
Danilone
Dindevan
Hedulin
Phenylindione
Athrombon
Danedion
Diophindane
Emandione
Fenhydren
Phenhydren
Phenillin
Theradione
Fenindion
Hemolidione
Phenyline
Danilon
Diadilan
Dineval
Emandion
Eridione
Fenilin
Phenylen
Phenylin
Pindione
Tromazal
Trombol
Bindan
Indema
Indon
Cronodione
Thrombasal
Indion
Fenindiona
2-Phenylindandione
2-Phenyl-1,3-diketohydrindene
Phenindionum
1H-Indene-1,3(2H)-dione, 2-phenyl-
Phenyllin
2-Phenyl-1,3-indanedione
2-phenylindene-1,3-dione
1,3-Indandione, 2-phenyl-
2-phenyl-2,3-dihydro-1H-indene-1,3-dione
2-Fenyloindandion-1,3
Fenindiona [INN-Spanish]
Phenindionum [INN-Latin]
2-phenyl-1,3(2H)-Indenedione
PID
HSDB 3155
2-Phenylindan-1,3-dione
EINECS 201-454-4
NSC 41693
NSC-41693
Phenindione (INN)
UNII-5M7Y6274ZE
CHEBI:8066
DTXSID5023453
5M7Y6274ZE
MFCD00003782
CHEMBL711
Phenindione [USP:INN:BAN]
MLS000069422
DTXCID803453
CAS-83-12-5
NCGC00016329-01
SMR000059058
PHENINDIONE [INN]
Fenindiona (INN-Spanish)
Phenindionum (INN-Latin)
PHENINDIONE (MART.)
PHENINDIONE [MART.]
Phenindione (USP:INN:BAN)
Fenindione
2-Fenyloindandion-1,3 [Polish]
2 Phenyl 1,3 indandione
2-phenylindane-1,3-dione
Hedulin (TN)
SR-01000721861
Phenindion
Prestwick_872
HEDUCIN
Phenindione (Standard)
Phenindione(Rectadione)
Spectrum_000927
Phenindione (Rectadione)
PHENINDIONE [MI]
Opera_ID_1966
Prestwick0_000538
Prestwick1_000538
Prestwick2_000538
Prestwick3_000538
Spectrum2_000999
Spectrum3_000710
Spectrum4_000476
Spectrum5_001070
P1029
Rectadione;phenylindandione
PHENINDIONE [HSDB]
2-Phenyl-indan-1,3-dione
1H-Indene-1, 2-phenyl-
Oprea1_684242
SCHEMBL33831
BSPBio_000555
BSPBio_002499
KBioGR_000952
KBioSS_001407
PHENINDIONE [WHO-DD]
MLS001148439
DivK1c_000307
SPECTRUM1500477
SPBio_001097
SPBio_002476
BPBio1_000611
GTPL6838
HMS500P09
HY-B0325R
KBio1_000307
KBio2_001407
KBio2_003975
KBio2_006543
KBio3_001719
B01AA02
PHENINDIONE [ORANGE BOOK]
NINDS_000307
WLN: L56 BV DV CHJ CR
2-PHENYLINDAN-1-3-DIONE
HMS1569L17
HMS1920F20
HMS2091N22
HMS2096L17
HMS2234N06
HMS3651M04
HMS3713L17
Pharmakon1600-01500477
2-Phenyl-1,3-indandione, 97%
HY-B0325
NSC41693
1,3(2H)-Indenedione, 2-phenyl-
Tox21_110375
BDBM50280157
CCG-40217
NSC757269
s1921
STK395038
AKOS000445019
Tox21_110375_1
DB00498
FP63877
NSC-757269
IDI1_000307
NCGC00016329-02
NCGC00016329-03
NCGC00016329-04
NCGC00016329-05
NCGC00016329-07
NCGC00094756-01
NCGC00094756-02
NCGC00094756-03
NCGC00094756-04
BS-18169
SY051560
SBI-0051480.P003
AB00052069
NS00003441
SW196997-3
C07584
D08354
D92057
EN300-123539
AB00052069_13
AB00052069_14
Q1640947
SR-01000721861-2
SR-01000721861-3
BRD-K70592963-001-21-7
BRD-K70592963-001-26-6
BRD-K70592963-001-27-4
BRD-K70592963-001-28-2
BRD-K70592963-001-29-0
BRD-K70592963-001-31-6
BRD-K70592963-001-32-4
Z276115700
201-454-4
InChI=1/C15H10O2/c16-14-11-8-4-5-9-12(11)15(17)13(14)10-6-2-1-3-7-10/h1-9,13
UAS
Solubility of 2-phenylindane-1,3-dione
The solubility of 2-phenylindane-1,3-dione (C15H10O2) can be quite intriguing, as it may vary significantly depending on the solvent and conditions used. Generally, this compound exhibits the following characteristics:
To summarize, while 2-phenylindane-1,3-dione may exhibit moderate solubility in non-polar organic solvents, its solubility in polar solvents remains quite limited—an important consideration for applications involving this intriguing compound.