Interesting facts
Interesting Facts About 2-phenyl-1H-benzimidazole
2-Phenyl-1H-benzimidazole is a fascinating compound with a variety of applications and properties that make it significant in both academic research and industrial applications. Here are some noteworthy aspects of this compound:
- Structure and Composition: The unique structure of 2-phenyl-1H-benzimidazole incorporates a benzimidazole backbone, which is a fused ring system that is known for its stability and reactivity. This core allows for interesting interactions with other chemical species.
- Biological Activity: Studies have shown that 2-phenyl-1H-benzimidazole exhibits noteworthy biological properties. It has been investigated for its potential as an anti-cancer agent, showcasing the promise of benzimidazole derivatives in medicinal chemistry.
- Fluorescent Properties: Many benzimidazole derivatives, including 2-phenyl-1H-benzimidazole, are praised for their fluorescent characteristics. This property can be exploited in fluorescence labeling used in imaging applications.
- Applications: Beyond its biological relevance, this compound has applications in several fields, including organic electronics and photovoltaic devices due to its semiconductor properties.
- Research Interest: The chemical community continues to explore 2-phenyl-1H-benzimidazole for various applications, driven by its potential to lead to new discoveries in drug development and material science.
"The study of compounds like 2-phenyl-1H-benzimidazole open up new frontiers in chemistry that blend the boundaries between organic synthesis and medicinal research."
Overall, 2-phenyl-1H-benzimidazole serves as a prime example of how a single compound can bridge numerous scientific disciplines, illustrating the importance of interdisciplinary approaches in modern chemistry.
Synonyms
2-Phenylbenzimidazole
716-79-0
2-Phenyl-1H-benzimidazole
2-phenyl-1H-benzo[d]imidazole
Phenizidole
Phenzidol
Phenzidole
Gainex
1H-Benzimidazole, 2-phenyl-
BENZIMIDAZOLE, 2-PHENYL-
NSC 251956
EINECS 211-939-2
CB9ZJ140SB
BRN 0007087
DTXSID5052460
NSC-251956
DTXCID2031033
5-23-08-00437 (Beilstein Handbook Reference)
N,N'-BENZENYL-O-PHENYLENEDIAMINE
2-PHENYL-1H-BENZIMIDAZOLE [MI]
2-phenyl-1H-benzo(d)imidazole
211-939-2
inchi=1/c13h10n2/c1-2-6-10(7-3-1)13-14-11-8-4-5-9-12(11)15-13/h1-9h,(h,14,15
2-Phenylbenzimdazole
2-Phenyl-1H-benzoimidazole
MFCD00005592
2-phenyl-1H-1,3-benzodiazole
UNII-CB9ZJ140SB
phenylbenzimidazole
phenyl benzimidazole
2-phenyl benzimidazole
2-phenyl-benzimidazole
1H-Benzimidazole, phenyl-
2-Phenylbenzimidazole, 97%
cid_12855
MLS000701325
BIDD:GT0186
SCHEMBL105095
BDBM3789
CHEMBL153535
HMS1728H19
HMS2235H23
HMS3372F02
ALBB-033235
BCP27606
Tox21_303711
BBL000186
g 570
NSC251956
STK227880
AKOS000275572
AC-7237
CS-W010651
NCGC00247174-01
NCGC00357026-01
AS-11952
CAS-716-79-0
SMR000526282
SY005301
NS00005205
P1105
EN300-16230
O10849
AB00876270-08
AF-407/01228019
BRD-K90551865-001-05-1
Q27275387
Z50129842
F0853-0315
Solubility of 2-phenyl-1H-benzimidazole
2-phenyl-1H-benzimidazole is a fascinating compound when it comes to its solubility properties. This compound exhibits moderate solubility in organic solvents, which is characteristic of many benzimidazole derivatives. Here are some key points regarding its solubility:
In summary, the solubility of 2-phenyl-1H-benzimidazole can be described as limited in aqueous environments, yet viable in organic solvents, making it essential for specific applications in medicinal chemistry and material science. Understanding these solubility characteristics is key for optimal formulation and utilization in various chemical processes.