-
Diethylaluminium cyanide ("Nagata's reagent") is the
organoaluminium compound with
formula ((C2H5)2AlCN)n. This
colorless compound is
usually handled as...
-
Diethylaluminium chloride,
abbreviated DEAC, is an
organoaluminium compound.
Although often given the
chemical formula (C2H5)2AlCl, it
exists as a dimer...
-
Partially or
fully alkylated derivatives of
metal and
nonmetal hydrides (
diethylaluminium hydride, trimethylaluminium, triethylaluminium, butyllithium), with...
-
discovered that a
combination of
titanium tetrachloride (TiCl4) and
diethylaluminium chloride (Al(C2H5)2Cl) gave
comparable activities for the production...
-
treatment with
active metals, such as
sodium or magnesium. For example,
diethylaluminium chloride or
triethylaluminium can be
produced from
ethylaluminium sesquichloride...
-
niche uses as a
precursor to
other organoaluminium compounds, such as
diethylaluminium cyanide: 1 2 Al 2 Et 6 + HCN ⟶ 1 n [ Et 2 AlCN ] n + C 2 H 6 {\displaystyle...
-
compound with the
chemical formula [(CH3)2AlCl]2. It
behaves similarly to
diethylaluminium chloride but is more expensive. Hence, it is less
commonly used. Like...
-
Number class Proper Shipping Name UN 1101 ? (UN No. no
longer in use)
Diethylaluminium chloride (UN No. no
longer in use) UN 1102 ? (UN No. no
longer in use)...
-
weight linear polyethylene in the
presence of
methylaluminoxane or
diethylaluminium chloride as cocatalysts. It does not
polymerize propylene....
-
vanadium complexes are
activated with
alkylaluminium chlorides, e.g.
diethylaluminium chloride. The
organoaluminium reagent installs alkyl groups on the...
