-
Fluorenone is an
organic compound with the
chemical formula (C6H4)2CO, a
ketone with
fluorene moiety. It is
bright fluorescent yellow solid. It is synthesised...
-
carbon between the two
benzene rings.
Hydroxyfluorene can be
converted to
fluorenone by oxidation. It is a white-cream
colored solid at room temperature. Fluorenol...
- diphenylmethane. Alternatively, it can be
prepared by the
reduction of
fluorenone with zinc or
hypophosphorous acid–iodine. The
fluorene molecule is nearly...
- the
Pschorr cyclization: The
group Z can be CH2, CH2CH2, NH and CO (to
fluorenone) to name just a few. Graebe–Ullmann
synthesis Meerwein arylation Sandmeyer...
- trioxide) by
sulfuric acid.
Sodium dichromate can be used in
fluorene to
fluorenone conversion. Like all
hexavalent chromium compounds,
sodium dichromate...
-
solutions of
rubicene emit
strong yellow fluorescence. It's
synthesized from
fluorenone by
reduction of
calcium or magnesium, or it can be
obtained by reacting...
-
addition to regioselectivity, the
degree of
nitration is of interest.
Fluorenone, for example, can be
selectively trinitrated or tetranitrated. The direct...
- 4394-00-7 C13H9N
acridine 260-94-6 C13H9N
phenanthridine 229-87-8 C13H9NO
fluorenone oxime 2157-52-0 C13H9P
acridophosphine 398-14-1 C13H10
fluorene 86-73-7...
-
discharge cycles in tests,
although it was not water-soluble.
Quinone and
fluorenone molecules can be
reengineered to
increase water solubility. In 2021 a...
- Wolff-Kishner reaction. 6.
Comparison of the
hydrazones of benzophenone,
fluorenone, dibenzotropone, and dibenzosuberone". The
Journal of
Organic Chemistry...
