Interesting facts
Interesting Facts About 5-Methyl-2-phenyl-4H-pyrazol-3-one
5-Methyl-2-phenyl-4H-pyrazol-3-one, often abbreviated as a complex pyrazolone, has garnered significant attention in various fields of chemistry due to its unique structure and diverse applications. Here are some engaging points about this intriguing compound:
- Structural Characteristics: The compound features a pyrazolone framework, characterized by a five-membered ring with two nitrogen atoms. The presence of both methyl and phenyl groups contributes to its chemical versatility.
- Biological Activity: Research has shown that derivatives of this pyrazolone exhibit notable biological activities, including anti-inflammatory and analgesic effects. This makes them valuable in medicinal chemistry.
- Applications in Organic Synthesis: 5-Methyl-2-phenyl-4H-pyrazol-3-one is often employed as a building block in organic synthesis, leading to the development of more complex molecules. Its reactivity allows for various functional group modifications.
- Role as a Ligand: This compound can act as a ligand in coordination chemistry, forming complexes with transition metals. Such metal complexes can have applications in catalysis and material science.
- Insights into Coordination Chemistry: The electron-donating properties of the nitrogen atoms in the pyrazolone ring enable interesting interactions with metal centers, leading to diverse coordination modes.
In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." Exploring compounds like 5-methyl-2-phenyl-4H-pyrazol-3-one embodies this philosophy, showcasing how one structure can lead to numerous innovative applications across different scientific domains.
As researchers continue to unveil the potential of pyrazolones, it is clear that this compound not only exemplifies the beauty of chemical diversity but also serves as a testament to the endless possibilities that lie within the realm of organic compounds.
Synonyms
edaravone
89-25-8
3-METHYL-1-PHENYL-2-PYRAZOLIN-5-ONE
Radicut
Norphenazone
1-Phenyl-3-methyl-5-pyrazolone
Developer Z
MCI-186
Methylphenylpyrazolone
C.I. Developer 1
Norantipyrine
Phenyl methyl pyrazolone
Phenylmethylpyrazolone
Radicava
3-Methyl-1-phenyl-5-pyrazolone
5-Methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one
3-Methyl-1-phenyl-1H-pyrazol-5(4H)-one
1-Phenyl-3-methyl-5-oxo-2-pyrazoline
CI Developer 1
1-Phenyl-3-methylpyrazolone
3H-Pyrazol-3-one, 2,4-dihydro-5-methyl-2-phenyl-
1-Phenyl-3-methylpyrazolone-5
2-Pyrazolin-5-one, 3-methyl-1-phenyl-
3-Methyl-1-phenylpyrazol-5-one
5-methyl-2-phenyl-4H-pyrazol-3-one
Colorex pmp
Jarocol pmp
3-Methyl-1-phenyl-2-pyrazoline-5-one
NCI-C03952
5-Pyrazolone, 3-methyl-1-phenyl-
2,4-Dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one
Edaravone (MCI-186)
NSC-2629
CCRIS 512
edaravona
NSC-26139
1-Fenyl-3-methyl-2-pyrazolin-5-on
CHEBI:31530
HSDB 4102
UNII-S798V6YJRP
EINECS 201-891-0
S798V6YJRP
MFCD00003138
BRN 0609575
DTXSID9021130
AI3-03557
3-methyl-1-phenyl-4,5-dihydro-1H-pyrazol-5-one
MLS000069602
3-METHYL-1-PHENYL-2-PYRAZOLIN-5-ONE (MCI-186)
DTXCID201130
EC 201-891-0
1-Phenyl-3-methyl-2-pyrazolin-5-one
NCGC00164015-01
SMR000059020
EDARAVONE (MART.)
EDARAVONE [MART.]
Edaravone [INN]
Monopyrazolone
WLN: T5NMV DHJ BR& E1
CAS-89-25-8
Radicut (TN)
PHENAZONE IMPURITY A (EP IMPURITY)
PHENAZONE IMPURITY A [EP IMPURITY]
3H-Pyrazol-3-one,4-dihydro-5-methyl-2-phenyl-
SR-01000000135
1-Fenyl-3-methyl-2-pyrazolin-5-on [Czech]
edaravonum
3-?Methyl-?1-?phenyl-?2-?pyrazolin-?5-?one(Edaravone)
MCI186
(Edaravone)
1 Phenyl 3 methyl 5 pyrazolone
Radicava (TN)
(MCI-186)
Edaravone (Standard)
3 Methyl 1 phenyl 2 pyrazolin 5 one
RADICAVA ORS
CDS1_000986
Spectrum_000267
Tocris-0786
EDARAVONE [JAN]
MCI-186; Edaravone
Edaravone [USAN:INN]
EDARAVONE [HSDB]
EDARAVONE [USAN]
Maybridge1_005738
Opera_ID_1057
Spectrum2_001574
Spectrum3_000971
Spectrum4_001091
Spectrum5_001217
NORPHENAZONE [MI]
M0687
EDARAVONE [WHO-DD]
N-DESMETHYLANTIPYRINE
SCHEMBL4704
BSPBio_001235
BSPBio_002601
KBioGR_000575
KBioGR_001502
KBioSS_000575
KBioSS_000747
AE-641/00371017
MLS001146878
MLS002415675
MLS006011753
DivK1c_001018
DivK1c_002026
SPECTRUM1503635
SPBio_001508
CHEMBL290916
1-pheny-3-methyl-5-pyrazolone
Edaravone (USAN/JP17/INN)
EDARAVONE [ORANGE BOOK]
BCBcMAP01_000127
GTPL11994
HMS503K17
HMS557M18
HY-B0099R
KBio1_001018
KBio2_000575
KBio2_000747
KBio2_003143
KBio2_003315
KBio2_005711
KBio2_005883
KBio3_001029
KBio3_001030
KBio3_001821
N07XX14
NSC2629
NINDS_001018
5-Methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one (Edaravone)
BCPP000246
Bio1_000438
Bio1_000927
Bio1_001416
Bio2_000448
Bio2_000928
HMS1362M17
HMS1792M17
HMS1990M17
HMS2234M19
HMS3266F04
HMS3403M17
HMS3411L05
HMS3654L15
HMS3675L05
HMS3884A11
Pharmakon1600-01503635
BCP26336
DZB76567
HY-B0099
NSC26139
Tox21_112077
Tox21_201747
Tox21_302819
BDBM50200541
CCG-39352
MSK000657
NSC758622
s1326
STK201315
1-Phenyl-3-methyl-2-pyrazolin-5-on
AKOS000313817
Tox21_112077_1
AC-4745
BCP9000635
CS-1832
DB12243
FE22642
NSC-758622
SB19128
IDI1_001018
IDI1_002203
NCGC00018218-01
NCGC00018218-02
NCGC00018218-03
NCGC00018218-04
NCGC00018218-05
NCGC00018218-06
NCGC00018218-07
NCGC00018218-08
NCGC00018218-10
NCGC00018218-17
NCGC00022665-02
NCGC00022665-04
NCGC00022665-05
NCGC00022665-06
NCGC00256515-01
NCGC00259296-01
SBI-0051836.P002
DB-002517
NS00002708
SW148216-2
5-methyl-2-phenyl-2,4-dihydro-3-pyrazolone
EN300-16234
3-Methyl-1-phenyl-2-pyrazoline-5-one, 99%
3-METHYL-1-PHENYL-2H-PYRAZOLIN-5-ONE
4E-901
5-methyl-2-phenyl-2,4-dihydro-pyrazol-3-one
D01552
D86209
1-PHENYL-3-METHYL-DELTA3-PYRAZOL-5-ONE
3-?Methyl-?1-?phenyl-?2-?pyrazolin-?5-?one
3-PYRAZOLIN-5-ONE, 3-METHYL-1-PHENYL-
AB00375776_14
AB00375776_15
2 4-Dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one
2,4-dihydro-2-phenyl-5-methyl-3H-pyrazol-3-one
Q335099
SR-01000000135-2
SR-01000000135-3
SR-01000000135-5
5-Methyl-2-phenyl-2,4-dihydro-3H-pyrazol-3-one #
BRD-K35458079-001-04-2
BRD-K35458079-001-12-5
BRD-K35458079-001-23-2
BRD-K35458079-001-27-3
BRD-K35458079-001-28-1
BRD-K35458079-001-29-9
BRD-K35458079-001-31-5
BRD-K35458079-001-33-1
Z50145861
F0391-0021
3-Methyl-1-phenyl-2-pyrazoline-5-one, SAJ special grade
3-Methyl-1-phenyl-2-pyrazoline-5-one, purum, >=98.0% (NT)
Phenazone impurity A, European Pharmacopoeia (EP) Reference Standard
InChI=1/C10H10N2O/c1-8-7-10(13)12(11-8)9-5-3-2-4-6-9/h2-6H,7H2,1H
2,4-Dihydro-5-methyl-2-phenyl-3H-pyrazol-3-one;1-Phenyl-3-methyl-1H-4,5-dihydropyrazol-5-one;Methylphenylpyrazolone
Solubility of 5-methyl-2-phenyl-4H-pyrazol-3-one (C15H12N2O)
The solubility of 5-methyl-2-phenyl-4H-pyrazol-3-one is an interesting aspect to explore. As a compound with both aromatic and nitrogen functionalities, its solubility characteristics can be intriguing. Here are some key points regarding its solubility:
In summary, while 5-methyl-2-phenyl-4H-pyrazol-3-one demonstrates some solubility in suitable solvents, its aromatic nature and nitrogen content play crucial roles in defining its overall solubility behavior. Evaluating this property is vital for any applications or research involving this compound.