Interesting facts
Interesting Facts about 4-(4-nitrophenyl)thiazol-2-amine
4-(4-nitrophenyl)thiazol-2-amine is a fascinating compound that belongs to the broad category of amines, which play a pivotal role in organic chemistry. Here are some intriguing aspects of this compound:
- Structural Significance: The compound features a thiazole ring, which is notable for its inclusion of both nitrogen and sulfur atoms within a five-membered ring. This unique structure contributes to the compound's reactivity and potential applications in various chemical reactions.
- Bioactivity: Compounds containing nitro groups, like the one found in this molecule, are often studied for their biological activity. Several nitro-substituted compounds have shown promising properties, including antimicrobial and anti-inflammatory activities.
- Applications: 4-(4-nitrophenyl)thiazol-2-amine and its derivatives are of interest in medicinal chemistry. Research has indicated that compounds with similar structures may act as potential drugs or lead compounds in the development of new therapies, particularly in tackling drug-resistant pathogens.
- Synthetic Utility: The synthesis of thiazole-containing compounds is a notable area of interest in organic synthesis. The presence of the nitrophenyl group may facilitate further functionalization, which enhances its utility as a precursor in organic transformations.
- Research Potential: With an increasing focus on thiophene and thiazole derivatives in the field of materials science, 4-(4-nitrophenyl)thiazol-2-amine could inspire innovations in organic electronics or photonic devices due to its intriguing electronic properties.
In conclusion, the study of 4-(4-nitrophenyl)thiazol-2-amine provides a perfect intersection of synthetic chemistry and biological research, showcasing how understanding fundamental chemical structures can lead to significant advancements in both fields. As noted by one researcher, “Every molecule tells a story, and the tale of 4-(4-nitrophenyl)thiazol-2-amine is just beginning.”
Synonyms
2104-09-8
2-Amino-4-(4-nitrophenyl)thiazole
2-Thiazolamine, 4-(4-nitrophenyl)-
2-Amino-4-(p-nitrophenyl)thiazole
THIAZOLE, 2-AMINO-4-(p-NITROPHENYL)-
DTXSID9039238
BRN 0200321
DTXCID6065
AI3-62320
2-amino-4-(para-nitrophenyl)thiazole
4-27-00-04961 (Beilstein Handbook Reference)
2-ANPT
4-(4-Nitrophenyl)-1,3-thiazol-2-amine
4-(4-Nitrophenyl)-2-thiazolamine
4-(4-Nitrophenyl)thiazol-2-ylamine
4-(4-nitrophenyl)thiazol-2-amine
MFCD00170222
V5F5REB7MT
4-(4-Nitro-phenyl)-thiazol-2-ylamine
2-amino-4-{4-nitrophenyl}-1,3-thiazole
2-Amino-4-(4-nitrophenyl)-1,3-thiazole
2-amino-4-(4'-nitrophenyl)-1,3-thiazole
CA-011
UNII-V5F5REB7MT
4-(4-nitrophenyl)-1,3-thiazole-2-ylamine
Cambridge id 5156331
Oprea1_115130
Oprea1_571013
Oprea1_795143
SCHEMBL1068291
2-amino-4-p-nitrophenylthiazole
CHEMBL1625396
ALBB-001538
Tox21_200846
BBL013896
STK036236
2-amino-4-(4-nitro-phenyl)-thiazole
AKOS000103470
AKOS015894706
Thiazole, 2-amino-4-(p-nitrophenyl)
MS-6235
NCGC00248850-01
NCGC00258400-01
AC-22761
CAS-2104-09-8
2-Amino-4-(4-nitrophenyl)thiazole, 96%
4-(4-Nitrophenyl)-1,3-thiazol-2-amine #
CS-0033854
EU-0036905
AMINO-4-(P-NITROPHENYL)THIAZOLE, 2-
EN300-02221
AB00074661-01
AB-601/30964017
SR-01000407645
SR-01000407645-1
F0777-0567
Solubility of 4-(4-nitrophenyl)thiazol-2-amine
The solubility of 4-(4-nitrophenyl)thiazol-2-amine is influenced by various factors, including its molecular structure and the presence of specific functional groups. Generally, this compound exhibits a level of solubility in polar solvents due to its amine group, which can engage in hydrogen bonding.
Key Points About Solubility:
“Understanding solubility is crucial for applications involving drug formulation and environmental chemistry.”
Therefore, when working with 4-(4-nitrophenyl)thiazol-2-amine, it is essential to take into account its solubility characteristics to optimize its usage in practical applications.