Interesting facts
Exploring 4-amino-N-(2-phenylpyrazol-3-yl)benzenesulfonamide
4-amino-N-(2-phenylpyrazol-3-yl)benzenesulfonamide is a fascinating compound that intersects the fields of pharmaceuticals and organic chemistry. This compound is particularly notable due to its diverse applications and the complexity of its structure. Here are some intriguing facts about this compound:
- Pharmaceutical Applications: This compound belongs to a class of sulfonamides, which have historically played a crucial role in medicinal chemistry. They're primarily known for their antibacterial properties, making them valuable in treating various infections.
- Structural Complexity: The presence of a pyrazole ring enhances its activity and selectivity. This five-membered aromatic ring is not only interesting from a synthetic perspective but also significant in designing drugs that target specific biological pathways.
- Targeted Therapeutics: Compounds of this category can act as enzyme inhibitors, potentially affecting several biological processes. They are often researched for their effectiveness in various therapeutic areas, including anti-inflammatory and anticancer treatments.
- Research Potential: The structure of 4-amino-N-(2-phenylpyrazol-3-yl)benzenesulfonamide is a subject of ongoing research. Scientists are continually exploring modifications to enhance efficacy and reduce side effects, showcasing the *dynamic nature of compound development*.
- Interdisciplinary Approach: Studying this compound requires knowledge from multiple scientific disciplines, including organic synthesis, medicinal chemistry, and molecular biology. This multidisciplinary interaction often sparks innovative research and collaborations.
In summary, 4-amino-N-(2-phenylpyrazol-3-yl)benzenesulfonamide is a remarkable compound with significant implications in medicinal chemistry. As scientists continue to unravel its potential, the exploration of its various effects presents opportunities for groundbreaking therapeutic advancements.
Synonyms
sulfaphenazole
526-08-9
Sulphaphenazole
Sulfabid
Sulfafenazol
Sulfaphenazol
Sulfaphenazon
4-Amino-N-(1-phenyl-1H-pyrazol-5-yl)benzenesulfonamide
Plisulfan
Raziosulfa
Sulphenazole
Depocid
Sulfaphenylpyrazole
Depotsulfonamide
Sulfaphenylpipazol
Sulfaphenazolum
Sulfafenazolo
Firmazolo
Paidazolo
Eftolon
Inamil
Isarol
Merian
Orisul
Microtan pirazolo
1-Phenyl-5-sulfanilamidopyrazole
5-Sulfanilamido-1-phenylpyrazole
Sulfaphenylpyrazol
Phenylsulfapyrazole
N'-(1-Phenylpyrazol-5-yl)sulfanilamide
Solfafenazolo
3-(p-Aminobenzenesulfonamido)-2-phenylpyrazole
Sulfafenazolo [Italian]
4-amino-N-(2-phenylpyrazol-3-yl)benzenesulfonamide
Benzenesulfonamide, 4-amino-N-(1-phenyl-1H-pyrazol-5-yl)-
Sulfafenazol [INN-Spanish]
Sulfaphenazol [INN-French]
Sulfaphenazolum [INN-Latin]
N1-(1-Phenylpyrazol-5-yl)sulfanilamide
UNII-0J8L4V3F81
N(sup 1)-(1-Phenylpyrazol-5-yl)sulfanilamide
4-amino-N-(1-phenyl-1H-pyrazol-5-yl)benzene-1-sulfonamide
EINECS 208-384-3
NSC-757859
Sulfaphenazole-d4
BRN 0308518
DTXSID2044131
CHEBI:77780
N(1)-(1-Phenylpyrazol-5-yl)sulfanilamide
0J8L4V3F81
MFCD00057226
Sulfanilamide, N(sup 1)-(1-phenylpyrazol-5-yl)-
CHEMBL1109
DTXCID0024131
5-25-09-00415 (Beilstein Handbook Reference)
NSC 757859
1420043-53-3
NCGC00015925-02
CAS-526-08-9
Solfafenazolo [DCIT]
Sulfafenazol (INN-Spanish)
Sulfaphenazol (INN-French)
Sulfaphenazolum (INN-Latin)
SULFAPHENAZOLE (MART.)
SULFAPHENAZOLE [MART.]
Orisulf
4-Amino-N-(2-phenyl-2H-pyrazol-3-yl)-benze-ne-13C6-sulfonamide
Isarol V
SMR000326684
Prestwick_454
SR-01000075649
Lopac-S-0758
Sulfaphenazole (JAN/INN)
Sulfonylpyrazol
Sulfaphenazole?
Sulfaphenazole [INN:BAN:JAN]
Sulfabid (TN)
Spectrum_001406
Prestwick0_000021
Prestwick1_000021
Prestwick2_000021
Prestwick3_000021
Spectrum2_001943
Spectrum3_001741
Spectrum4_000443
Spectrum5_001185
Sulfaphenazole (Standard)
Sulfaphenazole, >=98%
Sulfanilamide, N1-(1-phenylpyrazol-5-yl)-
Sulfaphenazole 100 microg/mL in Acetonitrile
SULFAPHENAZOLE [MI]
SULFAPHENAZOLE [INN]
SULFAPHENAZOLE [JAN]
Lopac0_001095
BSPBio_000081
BSPBio_003442
KBioGR_000826
KBioSS_001886
MLS000859612
MLS001056713
DivK1c_000303
SCHEMBL122040
SPECTRUM1501143
SPBio_002002
SPBio_002005
BPBio1_000091
SULFAPHENAZOLE [WHO-DD]
GTPL11352
HMS500P05
HY-B1218R
KBio1_000303
KBio2_001886
KBio2_004454
KBio2_007022
KBio3_002662
4-Amino-N-(1-phenyl-1H-pyrazol-5-yl)-benzenesulfonamide
4-Amino-N-(2-phenyl-2H-pyrazol-3-yl)-benzenesulfonamide
J01ED08
NINDS_000303
HMS1568E03
HMS1921J13
HMS2095E03
HMS2235J21
HMS3263K12
HMS3373E16
HMS3712E03
Pharmakon1600-01501143
Sulfaphenazole, >=98% (HPLC)
ALBB-025160
BCP27626
HY-B1218
STR05485
SULFAPHENAZOLE [ORANGE BOOK]
Tox21_110262
Tox21_501095
BDBM50090677
CCG-39431
NSC757859
Pyrazole, 1-phenyl-5-sulfanilamido-
s3673
STK663863
AKOS003348743
Tox21_110262_1
1ST4057
CS-4843
DB06729
FS35017
LP01095
SDCCGSBI-0051065.P004
IDI1_000303
NCGC00015925-01
NCGC00015925-03
NCGC00015925-04
NCGC00015925-05
NCGC00015925-06
NCGC00015925-07
NCGC00015925-08
NCGC00015925-09
NCGC00015925-10
NCGC00015925-12
NCGC00015925-13
NCGC00015925-17
NCGC00094368-01
NCGC00094368-02
NCGC00094368-03
NCGC00094368-04
NCGC00094368-05
NCGC00261780-01
DA-67841
SBI-0051065.P003
AB00052218
EU-0101095
NS00006369
BIM-0051065.0001
D01954
D70410
S 0758
AB00052218_10
EN300-7419010
Q6577293
SR-01000075649-2
SR-01000075649-7
SR-01000075649-8
SR-01000075649-9
BRD-K10671814-001-05-6
BRD-K10671814-001-09-8
BRD-K10671814-001-14-8
BRN-0308518; BRN0308518; BRN 0308518;Sulfabid;Sulfaphenylpyrazol;Sulphaphenazole
208-384-3
Solubility of 4-amino-N-(2-phenylpyrazol-3-yl)benzenesulfonamide
The solubility of 4-amino-N-(2-phenylpyrazol-3-yl)benzenesulfonamide, with the chemical formula C15H14N4O2S, can be complex and influenced by various factors. Here are some key points to consider:
In conclusion, while the solubility of 4-amino-N-(2-phenylpyrazol-3-yl)benzenesulfonamide is influenced by its functional groups and the solvent environment, it is essential to conduct empirical investigations to accurately determine its solubility parameters under various conditions.