Interesting facts
Interesting Facts about N-(4-Nitro-2-phenoxy-phenyl)methanesulfonamide
N-(4-nitro-2-phenoxy-phenyl)methanesulfonamide is a fascinating compound that belongs to the category of sulfonamides, well-known for their diverse applications, especially in pharmaceuticals. Here are some intriguing aspects of this compound:
- Pharmaceutical Relevance: Compounds in the sulfonamide class have played a crucial role in antimicrobial therapy, with historical significance dating back to the early 20th century.
- Structure and Function: The molecular structure features a sulfonamide functional group, which is essential for its biological activity, illustrating the importance of functional groups in chemistry. The presence of the nitro group can enhance the compound's reactivity and biological properties.
- Application Potential: Researchers are continually exploring the potential of such compounds in drug design, where modifications can lead to enhanced efficacy against various diseases.
- Environmental Considerations: The phenoxy group hints at many applications beyond pharmaceuticals, including agrochemicals, wherein the compound's properties can influence plant growth and pest resistance.
As noted by chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This compound exemplifies how modifying known chemical structures can lead to novel applications and ultimately improve our understanding of chemistry and its applicability.
In summary, N-(4-nitro-2-phenoxy-phenyl)methanesulfonamide serves as an excellent example of the intersection between organic chemistry and medicinal applications, showcasing the continuous innovation within the field.
Synonyms
nimesulide
51803-78-2
N-(4-Nitro-2-phenoxyphenyl)methanesulfonamide
Mesulid
Flogovital
Sulidene
Nimed
Nimesulida
4-NITRO-2-PHENOXYMETHANESULFONANILIDE
R-805
Methanesulfonamide, N-(4-nitro-2-phenoxyphenyl)-
Nimesulidum
R 805
4'-Nitro-2'-phenoxymethanesulfonanilide
Nisulid
4-Nitro-2-phenoxy-methanesulfonanilide
EINECS 257-431-4
UNII-V4TKW1454M
4'-Nitro-2'-phenoxymethansulfonanilid
NSC-758412
BRN 2421175
CCRIS 8225
V4TKW1454M
DTXSID3037250
CHEBI:44445
Methanesulfonanilide, 4'-nitro-2'-phenoxy-
MFCD00079470
CHEMBL56367
MLS000069680
DTXCID1017250
NSC 758412
NCGC00015725-02
SMR000058484
CAS-51803-78-2
NIMESULIDE (MART.)
NIMESULIDE [MART.]
NIMESULIDE (EP IMPURITY)
NIMESULIDE [EP IMPURITY]
NIMESULIDE (EP MONOGRAPH)
NIMESULIDE [EP MONOGRAPH]
Antifloxil
Guaxan
Nimesulidum [INN-Latin]
Nimesulida [INN-Spanish]
NIM
Nimesulide [INN:BAN]
SR-01000000218
Aldoron
Nimedex
Orthobid
Nise Gel
Nimesulide,(S)
N-(4-Nitro-2-phenoxyphenyl)methanesulfonamide;4-Nitro-2-phenoxymethane-sulfonamide;4'-Nitro-2'-phenoxymethanesulfonanilide
Prestwick_618
Nimesulide (Standard)
Spectrum_001577
NIMESULIDE [MI]
Nimesulide (JAN/INN)
NIMESULIDE [INN]
NIMESULIDE [JAN]
Opera_ID_1247
Prestwick0_000194
Prestwick1_000194
Prestwick2_000194
Prestwick3_000194
Spectrum2_001541
Spectrum3_001576
Spectrum4_000178
Spectrum5_000964
Lopac-N-1016
NIMESULIDE [WHO-DD]
Lopac0_000855
SCHEMBL24882
BSPBio_000147
BSPBio_001103
BSPBio_003112
KBioGR_000443
KBioGR_000695
KBioSS_000443
KBioSS_002057
MLS001148268
DivK1c_000693
SPECTRUM1503231
SPBio_001382
SPBio_002068
N-(4-nitro-2-phenoxyphenyl)
BPBio1_000163
GTPL7401
NIM-03
Nimesulide - Bio-X trade mark
BCBcMAP01_000034
HMS502C15
HY-B0363R
KBio1_000693
KBio2_000443
KBio2_002057
KBio2_003011
KBio2_004625
KBio2_005579
KBio2_007193
KBio3_000825
KBio3_000826
KBio3_002612
M01AX17
Nimesulide for peak identification
NINDS_000693
Bio2_000382
Bio2_000862
HMS1362G05
HMS1568H09
HMS1792G05
HMS1922K17
HMS1990G05
HMS2089B14
HMS2095H09
HMS2234K19
HMS3262L11
HMS3269G17
HMS3371J19
HMS3403G05
HMS3414P09
HMS3649A04
HMS3655D13
HMS3678P07
HMS3712H09
HMS3884C22
Pharmakon1600-01503231
BCP10076
FDC18022
HY-B0363
Tox21_110207
Tox21_301850
Tox21_500855
BDBM50056999
CCG-39319
EI-287
NSC758412
s2040
STL018679
AKOS015897356
Tox21_110207_1
AC-4524
DB04743
FN26223
KS-1277
LP00855
SDCCGSBI-0050831.P004
IDI1_000693
IDI1_002137
NCGC00015725-01
NCGC00015725-03
NCGC00015725-04
NCGC00015725-05
NCGC00015725-06
NCGC00015725-07
NCGC00015725-08
NCGC00015725-09
NCGC00015725-10
NCGC00015725-11
NCGC00015725-12
NCGC00015725-13
NCGC00015725-15
NCGC00015725-16
NCGC00015725-29
NCGC00021842-03
NCGC00021842-04
NCGC00021842-05
NCGC00021842-06
NCGC00021842-07
NCGC00021842-08
NCGC00255661-01
NCGC00261540-01
BN166246
Nimesulide 100 microg/mL in Acetonitrile
R805
N-(4-Nitro-2-Phenoxy)Methanesulfonanilide
SBI-0050831.P003
DB-052029
AB00052332
EU-0100855
N0984
NS00006725
SW196785-3
D01049
D70376
M02164
N 1016
Q20994
AB00052332-16
AB00052332_17
AB00052332_18
EN300-7388636
N-[4-nitro-2-(phenoxy)phenyl]methanesulfonamide
SR-01000000218-2
SR-01000000218-6
SR-01000000218-7
BRD-K76775527-001-06-2
BRD-K76775527-001-18-7
BRD-K76775527-001-28-6
BRD-K76775527-001-29-4
BRD-K76775527-001-30-2
SR-01000000218-11
Nimesulide, European Pharmacopoeia (EP) Reference Standard
Nimesulide, Pharmaceutical Secondary Standard; Certified Reference Material
Nimesulide for peak identification, European Pharmacopoeia (EP) Reference Standard
1364966-82-4
257-431-4
Solubility of N-(4-nitro-2-phenoxy-phenyl)methanesulfonamide
N-(4-nitro-2-phenoxy-phenyl)methanesulfonamide, with the chemical formula C13H12N2O5S, exhibits intriguing solubility characteristics due to its unique structural components. Understanding the solubility of this compound requires considering several factors:
As a general observation, compounds with similar structures often show variable solubility profiles, leading to statements such as: "The solubility can be case-dependent, influenced by temperature, pH, and solvent choice." In practice, N-(4-nitro-2-phenoxy-phenyl)methanesulfonamide is expected to have moderate solubility in polar solvents like methanol or ethanol and may be less soluble in non-polar organic solvents. Therefore, careful consideration should be given during experimental procedures to ensure proper solubility and utilization.