Interesting facts
Interesting Facts about 4-amino-N-(2-pyridyl)benzenesulfonamide
4-amino-N-(2-pyridyl)benzenesulfonamide, commonly known in various chemistry circles, is a fascinating compound with a range of significant applications and properties worth noting. This compound holds a prominent place in medicinal chemistry due to its potential pharmacological activities. Here are some intriguing aspects:
- Pharmaceutical Relevance: It is widely studied for its role as a sulfonamide antibiotic, which works by inhibiting bacterial growth. This mechanism makes it pivotal in treating bacterial infections.
- Structural Features: The compound has a unique structure featuring both a sulfonamide group and a pyridine moiety, which contribute to its biological activity. This combination often leads to enhanced interactions with biological targets.
- Research Interest: Ongoing research aims to explore its efficacy in treating not only bacterial infections but also potential applications in cancer therapy and other diseases, showcasing its versatile chemical nature.
- Potential Derivatives: The synthesis of derivatives of this compound has shown promise in creating new drugs with improved activity and reduced side effects, leading to a vibrant field of investigation in synthetic organic chemistry.
- Environmental Impact: Understanding the environmental fate and transport of sulfonamide compounds, including 4-amino-N-(2-pyridyl)benzenesulfonamide, is becoming increasingly important due to their widespread use in agriculture and healthcare.
In summary, 4-amino-N-(2-pyridyl)benzenesulfonamide is more than just a compound; it embodies a rich tapestry of chemical behaviors and applications that continue to inspire scientists and researchers alike. As stated by one prominent chemist, "The study of such compounds reveals the intricate dance of atoms and bonds that drives life itself."
Synonyms
sulfapyridine
144-83-2
Sulphapyridine
2-Sulfapyridine
2-Sulfanilamidopyridine
Sulfidin
Sulfidine
Streptosilpyridine
2-Sulfanilylaminopyridine
Coccoclase
Eubasinum
Haptocil
Piridazol
Plurazol
Pyridazol
Dagenan
Eubasin
Relbapiridina
Septipulmon
Sulfapiridina
Thioseptal
Adiplon
Pyriamid
Trianon
Ronin
2-Sulfanilamidopyridin
Solfapiridina
Sulfapyridinum
N-2-Pyridylsulfanilamide
N1-2-Pyridylsulfanilamide
4-amino-N-pyridin-2-ylbenzenesulfonamide
4-amino-N-(pyridin-2-yl)benzenesulfonamide
N(sup 1)-2-Pyridylsulfanilamide
2-(p-Aminobenzenesulphonamido)pyridine
4-amino-N-pyridin-2-yl-benzenesulfonamide
Benzenesulfonamide, 4-amino-N-2-pyridinyl-
2-Sulfanilyl aminopyridine
4-(2-Pyridinylsulfonyl)aniline
2-(4-Aminobenzenesulfonamido)pyridine
N(1)-Pyridylsulfanilamide
4-[(2-Pyridylamino)sulfonyl]aniline
M+B 693
N(sup1)-Pyridylsulfanilamide
N(1)-2-Pyridylsulfanilamide
Sulfanilamide, N1-2-pyridyl-
A-499
M&B 693
4-Amino-N,2-pyridinylbenzenesulfonamide
M and B 693
Sulfapyridinum [INN-Latin]
NSC 4753
Sulfapiridina [INN-Spanish]
M + B 693
NSC 41791
Sulfanilamide, N(sup 1)-2-pyridyl-
4-amino-N-(pyridin-2-yl)benzene-1-sulfonamide
CHEBI:132842
UNII-Y5V2N1KE8U
NSC-4753
EINECS 205-642-7
Y5V2N1KE8U
NSC-41791
4-AMINO-N-2-PYRIDINYLBENZENESULFONAMIDE
Sulfapyridine-13C6
DTXSID3026067
4-amino-n-(2-pyridinyl)benzenesulfonamide
AI3-01049
MLS000069725
DTXCID206067
Sulfapyridine [USP:INN:BAN]
Sulphapyridin
A 499
NSC4753
EC 205-642-7
NCGC00016408-01
Sulfanilamide, N1-2(1H)-pyridylidene-
CAS-144-83-2
SMR000058213
SULFAPYRIDINE MELTING POINT STANDARD
Solfapiridina [DCIT]
Sulfapyridinum (INN-Latin)
Sulfapiridina (INN-Spanish)
WLN: T6NJ BMSWR DZ
4-amino-N-(2-pyridyl)benzenesulfonamide
SULFAPYRIDINE (MART.)
SULFAPYRIDINE [MART.]
SULFAPYRIDINE (USP-RS)
SULFAPYRIDINE [USP-RS]
Sulfapyridine (USP:INN:BAN)
2-Sulfanilamidopyridin [German]
SULFAPYRIDINE (USP IMPURITY)
SULFAPYRIDINE [USP IMPURITY]
4-((2-Pyridylamino)sulfonyl)aniline
SULFAPYRIDINE (USP MONOGRAPH)
SULFAPYRIDINE [USP MONOGRAPH]
Sulfapyridine (TN)
4-Amino-n-2-pyridinyl-benzenesulfonamide
SULFASALAZINE IMPURITY J (EP IMPURITY)
SULFASALAZINE IMPURITY J [EP IMPURITY]
SR-01000000207
N'-2-Pyridylsulfanilide
Sulfapyridine (USP/INN)
ulfapyridine
Sulfapyridin
sulfapyridine III
SFY
ALBB-006215
MFCD00038036
Prestwick_1015
Spectrum_000996
Sulfapyridine (Dagenan)
Sulfapyridine (Standard)
Prestwick0_000762
Prestwick1_000762
Prestwick2_000762
Prestwick3_000762
Spectrum2_001323
Spectrum3_001773
Spectrum4_000346
Spectrum5_001182
SULFAPYRIDINE [MI]
CHEMBL700
Epitope ID:122235
Benzenesulfonamide, 4-amino-N-(2-pyridinyl)-
SULFAPYRIDINE [INN]
cid_5336
Sulfapyridine, >=99.0%
Oprea1_344996
SCHEMBL44219
BSPBio_000804
BSPBio_003265
KBioGR_000751
KBioSS_001476
AO-801/41077453
DivK1c_000216
SPECTRUM1500551
SPBio_001445
SPBio_002743
SULFAPYRIDINE [WHO-DD]
BPBio1_000886
BDBM39340
GECHUMIMRBOMGK-UHFFFAOYSA-
GTPL12698
HMS500K18
HY-B0212R
KBio1_000216
KBio2_001476
KBio2_004044
KBio2_006612
KBio3_002766
J01EB04
NINDS_000216
4-(2-Pyridinylsulfonyl)aniline #
HMS1570I06
HMS1921C03
HMS2092K05
HMS2097I06
HMS2233H20
HMS3372N13
HMS3714I06
Pharmakon1600-01500551
SULFAPYRIDINE [ORANGE BOOK]
HY-B0212
NSC41791
Tox21_110426
aniline, N-2-pyridyl-4-sulphamoyl-
CCG-39261
M&B693
NSC757329
s1617
STK292439
AKOS000121424
Tox21_110426_1
CS-2157
DB00891
FS27939
HS-0063
M&B-693
NSC-757329
IDI1_000216
UPCMLD0ENAT5889155:001
NCGC00016408-02
NCGC00016408-03
NCGC00016408-04
NCGC00016408-05
NCGC00016408-06
NCGC00016408-09
NCGC00016408-10
NCGC00022008-03
NCGC00022008-04
AC-26818
SBI-0051525.P003
4-azanyl-N-pyridin-2-yl-benzenesulfonamide
DB-042750
N1-2(1H)-PYRIDYLIDENESULFANILAMIDE
AB00052100
NS00000225
EN300-21145
Sulfapyridine 1000 microg/mL in Acetonitrile
D02434
AB00052100_14
AB00052100_15
benzenesulfonamide, 4-amino-N(S)-(2-pyridyl)-
A808279
Sulfapyridine, VETRANAL(TM), analytical standard
Q3976827
SR-01000000207-2
SR-01000000207-3
BRD-K41406082-001-05-5
BRD-K41406082-001-09-7
BRD-K41406082-001-15-4
BRD-K41406082-001-16-2
Z104492884
4-amino-N-(1,2-dihydropyridin-2-ylidene)benzenesulfonamide
Sulfapyridine, European Pharmacopoeia (EP) Reference Standard
4-Amino-N-(pyrimidin-2-yl) benzenesulfonamide (Sulfadiazine) (14)
Sulfapyridine, United States Pharmacopeia (USP) Reference Standard
4-Amino-N-2-pyridinylbenzenesulfonamide;2-Sulfanilamidopyridine;2-Sulfapyridine
Sulfapyridine Melting Point Standard, United States Pharmacopeia (USP) Reference Standard
205-642-7
InChI=1/C11H11N3O2S/c12-9-4-6-10(7-5-9)17(15,16)14-11-3-1-2-8-13-11/h1-8H,12H2,(H,13,14)
Sulfapyridine melting point standard, Pharmaceutical Secondary Standard; Certified Reference Material
Solubility of 4-amino-N-(2-pyridyl)benzenesulfonamide (C11H11N3O2S)
The solubility of 4-amino-N-(2-pyridyl)benzenesulfonamide in various solvents is an interesting subject due to its specific chemical structure. This compound exhibits moderate solubility characteristics, largely influenced by the presence of both polar and non-polar functional groups. Here are some key points regarding its solubility:
To summarize, the solubility of 4-amino-N-(2-pyridyl)benzenesulfonamide can be described as:
Understanding these solubility characteristics is crucial for applications in pharmaceuticals and materials science, enabling researchers to predict behavior in different environments. As the saying goes, "Like dissolves like," and this compound showcases the nuances of that principle well.