Interesting facts
Interesting Facts about 4-amino-N-thiazol-2-yl-benzenesulfonamide
4-amino-N-thiazol-2-yl-benzenesulfonamide, often referred to in scientific literature as a compound with significant pharmaceutical implications, is a fascinating example of how small changes in molecular structure can lead to major differences in biological activity. Here are some key insights:
- Pharmaceutical Applications: This compound belongs to a class of molecules with potential use as antibacterial agents. Its unique structure allows it to inhibit bacterial growth, which is crucial in the development of new antibiotics.
- Thiazole Ring Benefits: The thiazole moiety in its structure has been extensively studied for its role in medicinal chemistry. It enhances the compound's interaction with biological targets, leading to higher efficacy in treatments.
- Dual Functionality: 4-amino-N-thiazol-2-yl-benzenesulfonamide showcases not only antibacterial properties but may also possess antivirulent characteristics. This dual functionality opens new avenues in infectious disease management.
- Sulfonamide Derivative: As a derivative of sulfonamides, this compound contributes to the ongoing exploration of sulfa drugs, which were among the first antibiotics ever developed. The persistence of sulfonamides in modern medicine is a testament to their significance.
In summary, the exploration of compounds like 4-amino-N-thiazol-2-yl-benzenesulfonamide is critical for the future of drug development. As chemists continue to uncover the mechanisms of action and optimize structure-activity relationships, this compound could play a vital role in combating resistant strains of bacteria. "The molecular diversity in medicinal compounds opens infinite possibilities for innovation."
Synonyms
sulfathiazole
72-14-0
Sulphathiazole
Sulfathiazol
Thiazamide
Sulfanilamidothiazole
2-Sulfanilamidothiazole
Norsulfazole
Norsulfasol
2-Sulfonamidothiazole
4-Amino-N-(thiazol-2-yl)benzenesulfonamide
Neostrepsan
Sulfatiazol
Sulfocerol
Thiozamide
Sulzol
2-(Sulfanilylamino)thiazole
Formosulfathiazole
Sulfathiazolum
Azoquimiol
Azoseptale
Cerazole
Chemosept
Eleudron
Estafilol
Norsulfazol
Planomide
Poliseptil
Sanotiazol
Septozol
Thiacoccine
Thiasulfol
Wintrazole
2-Sulfanilamidothiazol
Cibazol
Duatok
Dulana
Coco-Thiazole
2-(p-Aminobenzenesulfonamido)thiazole
N(1)-2-Thiazolylsulfanilamide
Streptosilthiazole
4-Amino-N-2-thiazolylbenzenesulfonamide
Sulfamul
Usaf sn-9
Cerazol (suspension)
2-(p-Aminobenzenesulphonamido)thiazole
Norsulfazolum
Ciba 3714
N1-(2-Thiazolyl)sulfanilamide
4-Amino-N-(1,3-Thiazol-2-Yl)Benzene-1-Sulfonamide
Solfatiazolo
N1-2-Thiazolylsulfanilamide
M&B 760
Caswell No. 809B
4-Amino-N-(1,3-thiazol-2-yl)benzenesulfonamide
Benzenesulfonamide, 4-amino-N-2-thiazolyl-
Sulfanilamide, N1-2-thiazolyl-
RP 2090
N(sup 1)-2-Thiazolylsulfanilamide
2090 R.P.
CCRIS 765
sulfthiazole
CHEBI:9337
4-amino-N-1,3-thiazol-2-ylbenzenesulfonamide
2090 rp
M+B 760
UNII-Y7FKS2XWQH
Y7FKS2XWQH
HSDB 4380
2-Sulfathiazole
4-Amino-N-thiazol-2-yl-benzenesulfonamide
Sulfanilamide, N(1)-2-thiazolyl-
Sulfathiazol [INN-French]
Sulfatiazol [INN-Spanish]
EINECS 200-771-5
Sulfathiazolum [INN-Latin]
NSC 31812
NSC-31812
Triple sulfa (sulfathiazole)
EPA Pesticide Chemical Code 077903
NSC 683531
NSC-683531
Sulfanilamide, N(sup 1)-2-thiazolyl-
DTXSID8026068
AI3-01050
Sodium sulfathiazole
MFCD00005319
CHEMBL437
DTXCID606068
N'-(2-Thiazolyl)sulfanilamide
Sulfathiazole [USP:INN:BAN]
N(sup1)-(2-Thiazolyl)sulfanilamide
TRYSUL COMPONENT SULFATHIAZOLE
NSC683531
Sulfanilamide, N(sup1)-2-thiazolyl-
SULTRIN COMPONENT SULFATHIAZOLE
VAGILIA COMPONENT SULFATHIAZOLE
CAS-72-14-0
GYNE-SULF COMPONENT SULFATHIAZOLE
NCGC00016309-02
NCGC00016309-06
4-Amino-N-(2-thiazolyl)benzenesulfonamide
Sulfanilamide, N1-4-thiazolin-2-ylidene-
Sulfathiazole 100 microg/mL in Acetonitrile
Sulfathiazol (INN-French)
Sulfatiazol (INN-Spanish)
Sulfathiazolum (INN-Latin)
SULFATHIAZOLE (MART.)
SULFATHIAZOLE [MART.]
SULFATHIAZOLE (USP-RS)
SULFATHIAZOLE [USP-RS]
Sulfathiazole (USP:INN:BAN)
Solfatiazolo [DCIT]
SULFATHIAZOLE (EP MONOGRAPH)
SULFATHIAZOLE [EP MONOGRAPH]
SULFATHIAZOLE (USP MONOGRAPH)
SULFATHIAZOLE [USP MONOGRAPH]
2-Sulfanilamidothiazol [German]
SR-05000001722
sulfatiazolo
Sulfathiazole; 4-Amino-N-(thiazol-2-yl)benzenesulfonamide
Enterobiocine
Sulfavitina
Cerazol
Sulfaplex
YTZ
Prestwick_430
Spectrum_001000
4-amino-N-2-thiazolyl Benzenesulfonamide
Benzenesulfonamide, 4 amino N 2 thiazolyl
Benzenesulfonamide, 4-amino-N-2-thiazolyl
Sulfathiazole (Standard)
Prestwick0_000016
Prestwick1_000016
Prestwick2_000016
Prestwick3_000016
Spectrum2_000841
Spectrum3_001729
Spectrum4_000348
Spectrum5_001441
Sulfathiazole (USP/INN)
N-2-Thiazolylsulfanilamide
SULFATHIAZOLE [MI]
Epitope ID:122234
SULFATHIAZOLE [INN]
Cambridge id 5251400
cid_5340
SULFATHIAZOLE [HSDB]
Oprea1_105970
Oprea1_297844
SCHEMBL94165
BSPBio_000051
BSPBio_003378
KBioGR_000755
KBioSS_001480
SULFATHIAZOLE [VANDF]
[(4-Aminophenyl)sulfonyl]-1,3-thiazol-2-ylamine
MLS002154174
N-1-2-Thiazolylsulfanilamide
DivK1c_000560
SPECTRUM1500553
SPBio_000821
SPBio_001972
SULFATHIAZOLE [WHO-DD]
BPBio1_000057
WLN: T5N CSJ BMSWR DZ
GTPL12699
HMS501L22
HY-B0507R
KBio1_000560
KBio2_001480
KBio2_004048
KBio2_006616
KBio3_002598
D06BA02
J01EB07
N(sup1)-2-Thiazolylsulfanilamide
NINDS_000560
HMS1568C13
HMS1921C07
HMS2092K09
HMS2095C13
HMS2259A13
HMS3652A03
HMS3712C13
Pharmakon1600-01500553
SULFATHIAZOLE [GREEN BOOK]
SULFATHIAZOLE [ORANGE BOOK]
HY-B0507
NSC31812
SULFATHIAZOLE (TRIPLE SULFA)
Tox21_110363
Tox21_202243
Tox21_303238
BDBM50027796
CCG-40296
NSC757331
s3116
STK043870
2-(4-Aminobenzenesulfonamido)thiazole
AKOS000108630
Tox21_110363_1
DB06147
FS27944
NSC-757331
SDCCGMLS-0065585.P001
IDI1_000560
N(SUP1)-2-THIAZOYLSULFANILAMIDE
SULFATHIAZOLE COMPONENT OF TRYSUL
NCGC00016309-01
NCGC00016309-03
NCGC00016309-04
NCGC00016309-05
NCGC00016309-07
NCGC00016309-08
NCGC00016309-09
NCGC00016309-10
NCGC00016309-14
NCGC00091133-01
NCGC00091133-02
NCGC00091133-03
NCGC00091133-04
NCGC00257187-01
NCGC00259792-01
SULFATHIAZOLE COMPONENT OF SULTRIN
SULFATHIAZOLE COMPONENT OF VAGILIA
AC-12783
DS-17245
NCI60_002730
SMR000017368
Pyridine,2-(chloromethyl)-3,4-dimethoxy-
SBI-0051527.P004
thiazole, 2-(p-amino)benzenesulphonamido-
DB-055610
SULFATHIAZOLE COMPONENT OF GYNE-SULF
4-amino-N-(thiazol-2-yl)-benzenesulfonamide
AB00052102
N-(2-Thiazolyl)benzenesulfonamide, 4-amino-
NS00000201
SW149625-4
4-[(1,3-Thiazol-2-yl)aminosulfonyl]aniline
EN300-18132
Sulfathiazole 1000 microg/mL in Acetonitrile
Sulfathiazole, analytical standard, >=98.0%
D01047
D70411
AB00052102_14
AB00052102_15
Q408427
Sulfathiazole, VETRANAL(TM), analytical standard
TRIPLE SULFA (SULFATHIAZOLE) [ORANGE BOOK]
4-Amino-N-(1,3-thiazol-2-yl)benzenesulfonamide #
SR-05000001722-1
SR-05000001722-3
BRD-K14705039-001-05-7
BRD-K14705039-001-08-1
BRD-K14705039-001-15-6
BRD-K14705039-001-16-4
Z57198680
F1443-4816
Sulfathiazole, European Pharmacopoeia (EP) Reference Standard
Sulfathiazole, United States Pharmacopeia (USP) Reference Standard
200-771-5
Solubility of 4-amino-N-thiazol-2-yl-benzenesulfonamide
The solubility of a chemical compound is a crucial aspect that governs its applications in various fields, including pharmaceuticals and industrial processes. For 4-amino-N-thiazol-2-yl-benzenesulfonamide (C9H9N3O2S2), the solubility characteristics can be summarized as follows:
In conclusion, the solubility of 4-amino-N-thiazol-2-yl-benzenesulfonamide is influenced by multiple factors such as solvent choice, temperature, pH, and polarity. Understanding these factors is essential for optimizing its use in various applications.