Interesting facts
Interesting Facts About 9H-fluoren-2-amine
9H-fluoren-2-amine, often simply referred to as fluoren-2-amine, is a captivating compound that sits at the intersection of organic chemistry and material science. Here are some compelling facts that showcase its importance:
- Structure and Aromaticity: The structure of 9H-fluoren-2-amine features a fluorenyl group, which is a fused bicyclic aromatic compound. This unique arrangement imparts strong aromatic characteristics, making it quite stable and integral in various chemical reactions.
- Chemical Reactivity: As an amine, it can participate in a *variety of chemical reactions*, including nucleophilic substitutions and couplings. This versatility makes it a valuable precursor in organic synthesis.
- Applications in Material Science: Due to its distinct electronic properties, 9H-fluoren-2-amine is often utilized in the development of **organic light-emitting diodes (OLEDs)** and other optoelectronic materials, showcasing its relevance in modern technology.
- Role in Medicinal Chemistry: This compound has garnered attention for its potential agrochemical and pharmaceutical applications. It can serve as a starting material for the synthesis of bioactive compounds with *medicinal properties*.
- Historical Importance: The study of fluorenes dates back to the early 20th century, contributing significantly to the development of synthetic methodologies in organic chemistry.
In conclusion, 9H-fluoren-2-amine exemplifies the interplay between structure and function in organic compounds. Its applications span from electronics to pharmaceuticals, paving the way for innovations in multiple scientific fields.
Synonyms
2-aminofluorene
9H-Fluoren-2-amine
153-78-6
2-Fluorenamine
Aminofluoren
Fluorene, 2-amino-
2-Fluoreneamine
Fluoren-2-amine
2-Fluorenylamine
2-Fluroenylamine
Fluoren-2-ylamine
Aminofluoren [German]
CCRIS 31
HSDB 4026
EINECS 205-817-8
NSC 12274
UNII-3A69OS195N
BRN 1945861
DTXSID1049223
3A69OS195N
MFCD00001125
NSC-12274
AMINOFLUORENE, 2-
2-AMINOFLUORENE [HSDB]
DTXCID3029079
4-12-00-03370 (Beilstein Handbook Reference)
AMINOFLUOREN (GERMAN)
WLN: L B656 HHJ EZ
9H-Fluoren-2-ylamine
2Fluorenylamine
Fluoren2ylamine
2Fluorenamine
2Fluoreneamine
Fluoren2amine
2-Aminoflurene
9HFluoren2amine
2-amino-fluorene
Fluorene, 2amino
Fluorene, 2-amino
2-Amino-9H-fluorene
9H-fluoren-2-yl-amine
2-Aminofluorene, 98%
N-2-FLUORENYLAMINE
Oprea1_099026
MLS000589201
CHEMBL84472
SCHEMBL225901
SCHEMBL4185603
SGCUT00125
HMS1608K17
HMS2538L16
KNA08108
NSC12274
NSC26328
to_000026
Tox21_202971
NSC-26328
STK093094
AKOS000111311
AC-4871
CS-W017149
FA33811
HY-W016433
NCGC00246308-01
NCGC00260517-01
AS-14460
BP-12358
CAS-153-78-6
NCI60_000536
PD196987
SMR000219736
SY049251
DB-043201
A0621
EU-0034581
NS00024998
EN300-17389
D70520
SR-01000398070
SR-01000398070-1
Q26840753
F0037-4040
205-817-8
Solubility of 9H-Fluoren-2-amine (C13H11N)
9H-fluoren-2-amine is an organic compound whose solubility can be influenced by various factors including temperature, pH, and the presence of other solvents. Below are some key points regarding its solubility:
In summary, while 9H-fluoren-2-amine possesses certain solubility traits, its behavior can be versatile based on the environment it is placed in. Understanding these aspects is crucial for its effective use in chemical processes.