Interesting facts
Interesting Facts about 5,5-Diphenylimidazolidine-2,4-dione
5,5-Diphenylimidazolidine-2,4-dione, often referred to as a versatile compound in organic chemistry, belongs to the imidazolidine class of compounds. This specific compound is notable for its unique structure and chemical properties, which contribute to its various applications in scientific research and industrial processes.
Chemical Structure and Features
The compound contains:
- Two phenyl groups that enhance its reactivity and provide unique electronic properties.
- A cyclic imidazolidine ring that is characteristic of its chemical family.
- Multiple keto groups, which play a crucial role in its stability and reactivity.
Applications
The diverse applications of 5,5-diphenylimidazolidine-2,4-dione include:
- Synthesis of pharmaceuticals: It is often used as an intermediate in the formulation of various medicinal compounds.
- Research in organic chemistry: The compound serves as a useful model for studying reaction mechanisms and chemical behavior.
- Polymer chemistry: Its properties make it a candidate for the development of advanced materials with specific characteristics.
Scientific Significance
As a scientist or chemistry student, one might find this compound particularly interesting for several reasons:
- The compound is a fine example of how molecular structure can influence reactivity and application.
- Studies involving this compound can lead to a deeper understanding of non-covalent interactions, further enhancing its applicability in biological systems.
- It demonstrates the balance between stability and reactivity, showcasing a critical concept in chemical synthesis.
In conclusion, 5,5-diphenylimidazolidine-2,4-dione is more than just a compound; it’s a fundamental building block with extensive potential in both academic and industrial chemistry. Its ability to bridge various fields makes it a fascinating subject of study!
Synonyms
phenytoin
5,5-DIPHENYLHYDANTOIN
57-41-0
Diphenylhydantoin
Dilantin
5,5-diphenylimidazolidine-2,4-dione
Phenytoine
Zentropil
Epamin
Lepitoin
Dihydantoin
Diphenylan
Dilabid
Aleviatin
Difenin
Diphantoin
Fenitoina
Phentytoin
Diphedan
Fenylepsin
Sodanton
Dihycon
Lehydan
Dilantin acid
Diphenylhydatanoin
Dantoinal
Di-Hydan
Dilantine
Dillantin
Diphenine
Diphentyn
Ditoinate
Elepsindon
Epilantin
Fenytoine
Hidantilo
Hidantina
Hidantomin
Hydantoinal
Kessodanten
Phanantin
Phanatine
Phenatoine
Sodantoin
Sylantoic
Thilophenyl
Zentronal
Auranile
Dantinal
Dantoine
Difetoin
Difhydan
Dintoin
Dintoina
Diphedal
Diphenin
Enkelfel
Epifenyl
Epihydan
Fentoin
Hidantal
Hydantal
Hydantol
Idantoil
Idantoin
Labopal
Phentoin
Ritmenal
Saceril
Sanepil
Silantin
Solantin
Danten
Denyl
Epelin
Epinat
Epised
Eptal
Hidan
Lepsin
Oxylan
Ekko
Ictalis simple
Toin unicelles
Dantoinal klinos
Om-Hydantoine
Di-Phetine
Epdantoine simple
Hidantina vitoria
Gerot-epilan-D
Epilan-D
2,4-Imidazolidinedione, 5,5-diphenyl-
Neosidantoina
Comitoina
Epanutin
Hidantina senosian
Minetoin
Novantoina
Phenhydanin
Phenytoinum
Sinergina
Sodanthon
Causoin
Convul
Iphenylhydantoin
Di-Lan
Ekko capsules
Neos-Hidantoina
Phenytoin-Gerot
Difenilhidantoina
Fenytoin Dak
Epdantoin Simple
Dilantin-125
Om hidantoina simple
Phenytoin AWD
Didan TDC 250
Epilan D
TOIN
Novophenytoin
Hindatal
Phenytex
5,5-Diphenyl-2,4-imidazolidinedione
Fenitoina [INN-Spanish]
Phenytoine [INN-French]
Phenytoinum [INN-Latin]
Citrulliamon
Diphentoin
Diphenat
Hydantin
Phenitoin
Difenilhidantoina [Spanish]
Diphenylhydantoine [French]
Fenidantoin s
Fenantoin Mn Pharma
Diphenylhydantoine
Epasmir 5
5,5-Dwufenylohydantoina
Antisacer
Diphenylhydantoin (VAN)
Eptoin
DILANTIN-30
Di-Lan (VAN)
PHENYTOIN SODIUM
Solantoin
Solantyl
5,5-Diphenylimidazolidin-2,4-dione
DPH (VAN)
5,5-Diphenylhydantoin (IUPAC)
Didan-tdc-250
5,5-Diphenyl-imidazolidine-2,4-dione
CCRIS 515
5,5-diphenyl hydantoin
CHEBI:8107
Dilantin (TN)
5,5-Dwufenylohydantoina [Polish]
Hydantoin, 5,5-diphenyl-
NCI-C55765
5,5-Diphenylhydantoin (phenytoin)
AI3-52498
NSC 8722
NSC-8722
EINECS 200-328-6
MFCD00005264
DTXSID8020541
HSDB 3160
6158TKW0C5
SM-88 COMPONENT PHENYTOIN
PHENYTOIN [INN]
PHENYTOIN [JAN]
PHENYTOIN [MI]
PHENYTOIN [HSDB]
PHENYTOIN [IARC]
PHENYTOIN [USAN]
5,5-diphenyltetrahydro-1H-2,4-imidazoledione
Fenitoin
PHENYTOIN [VANDF]
PHENYTOIN [MART.]
Phenytoin [USAN:USP:INN:BAN:JAN]
PHENYTOIN [USP-RS]
PHENYTOIN [WHO-DD]
PHENYTOIN [WHO-IP]
DTXCID60541
MLS000069789
PHENYTOIN [ORANGE BOOK]
PHENYTOIN [EP MONOGRAPH]
PHENYTOIN [USP IMPURITY]
PHENYTOIN [USP MONOGRAPH]
NSC8722
PHENYTOINUM [WHO-IP LATIN]
Dilantin Infatabs
5,5-di(phenyl)imidazolidine-2,4-dione
NCGC00021139-03
SMR000059026
PHENYTOIN (IARC)
Fenitoina (INN-Spanish)
Phenytoine (INN-French)
Phenytoinum (INN-Latin)
PHENYTOIN (MART.)
Fenidantoin "s"
PHENYTOIN (USP-RS)
5,5-DIPHENYLHYDANTOIN-D5 98 ATOM % D
Epasmir "5"
PHENYTOIN (EP MONOGRAPH)
PHENYTOIN (USP IMPURITY)
PHENYTOIN (USP MONOGRAPH)
Phenytoin (USAN:USP:INN:BAN:JAN)
CAS-57-41-0
phenytoin (PHN)
component of Mebroin
fenidantoin ''s''
epasmir ''5''
Redox-phenytoin
UNII-6158TKW0C5
SR-01000075211
IFLab1_000214
Fenidantoin 's'
Phenytoin Infatabs
Episar (Salt/Mix)
Epasmir '5'
Aladdin (Salt/Mix)
Alepsin (Salt/Mix)
Epsolin (Salt/Mix)
Phenytoin (Lepitoin)
Phenytoin (Standard)
Tacosal (Salt/Mix)
Antisacer (Salt/Mix)
Epdantoin (Salt/Mix)
Epileptin (Salt/Mix)
Hydantoin,5-diphenyl-
FENIDANTOIN "S
Spectrum_001105
Fenigramon (Salt/Mix)
Citrullamon (Salt/Mix)
Opera_ID_394
2, 5,5-diphenyl-
CHEMBL16
Spectrum2_001281
Spectrum3_000890
Spectrum4_000984
Spectrum5_001369
Lopac-D-4007
EPASMIR "5
Epitope ID:117723
D 4007
SCHEMBL3440
BIDD:PXR0090
Lopac0_000329
Lopac0_000378
Oprea1_373280
PR-122 (redox-phenytoin)
BSPBio_001437
KBioGR_001387
KBioSS_001585
MLS001074087
MLS002454401
BIDD:GT0625
DivK1c_000507
Soluble phenytoin (Salt/Mix)
SPBio_001281
Phenytoin (JP18/USP/INN)
Phenytoin, 1mg/ml in Methanol
GTPL2624
2-hydroxy-5,5-diphenyl-3,5-dihydro-4H-imidazol-4-one
HY-B0448R
KBio1_000507
KBio2_001585
KBio2_004153
KBio2_006721
KBio3_001780
N03AB02
WLN: T5MVMV EHJ ER& ER
5,5-Diphenylhydantoin, >=99%
NINDS_000507
Phenytoin 1.0 mg/ml in Methanol
HMS1412J16
HMS1694O05
HMS1791H19
HMS1989H19
HMS2089E11
HMS2236J06
HMS3261K17
HMS3402H19
HMS3657O03
BCP05960
HY-B0448
Hydantoin, 5,5-diphenyl- (8CI)
Tox21_110861
Tox21_202299
Tox21_300281
Tox21_500378
AC-376
BDBM50003655
BDBM50101816
s2525
STK058029
STK182871
STL454130
AKOS000416887
AKOS003245432
Tox21_110861_1
CCG-104011
CCG-221682
DB00252
FD22484
LP00378
Phenytoin 1000 microg/mL in Methanol
IDI1_000507
IDI1_008433
NCGC00015342-01
NCGC00015342-02
NCGC00015342-03
NCGC00015342-04
NCGC00015342-05
NCGC00015342-06
NCGC00015342-07
NCGC00015342-08
NCGC00015342-09
NCGC00015342-10
NCGC00015342-11
NCGC00015342-12
NCGC00021139-01
NCGC00021139-02
NCGC00021139-04
NCGC00021139-05
NCGC00021139-06
NCGC00021139-07
NCGC00021139-08
NCGC00021139-09
NCGC00021139-10
NCGC00021139-11
NCGC00091492-01
NCGC00091492-02
NCGC00091492-03
NCGC00091492-04
NCGC00091492-05
NCGC00093810-01
NCGC00093810-02
NCGC00254135-01
NCGC00259848-01
NCGC00261063-01
5,5-?Diphenyl-?2,4-?imidazolidinedione
DA-56808
imidazolidine-2,4-dione, 5,5-diphenyl-
5,5-Diphenyl-1H-imidazolidine-2,4-dione
D0894
EU-0100378
NS00010290
SW203757-2
EN300-16818
5,5-Diphenyl-2,4-imidazolidinedione;Phenytoin
C07443
D00512
E76094
2,4-Imidazolidinedione, 5,5-diphenyl- (9CI)
AB00374253-10
AB00374253-11
AB00374253_13
Q410400
SR-01000003141
SR-01000003141-8
SR-01000075211-2
BRD-K55930204-001-02-7
BRD-K55930204-001-20-9
BRD-K55930204-236-11-0
BRD-K55930204-236-23-5
BRD-K55930204-236-24-3
Z56786458
4-hydroxy-5,5-diphenyl-1,5-dihydro-2H-imidazol-2-one
F0020-1370
Phenytoin, European Pharmacopoeia (EP) Reference Standard
Phenytoin, United States Pharmacopeia (USP) Reference Standard
Phenytoin, Pharmaceutical Secondary Standard; Certified Reference Material
Phenytoin for system suitability, European Pharmacopoeia (EP) Reference Standard
200-328-6
Solubility of 5,5-Diphenylimidazolidine-2,4-dione
5,5-Diphenylimidazolidine-2,4-dione, with the chemical formula C15H12N2O2, exhibits interesting solubility characteristics influenced by its molecular structure. Here’s an overview of its solubility:
In conclusion, while 5,5-diphenylimidazolidine-2,4-dione can exhibit solubility in several organic solvents, its overall solubility profile will depend on the specific conditions and solvent interactions. As noted, "Solubility is not just a property; it's an intricate dance of molecular interactions."