-
Organoiodine chemistry is the
study of the
synthesis and
properties of
organoiodine compounds, or organoiodides,
organic compounds that
contain one or...
- hydrophobic. The
melting and
boiling points of chloro-, bromo-, and
iodoalkanes are
higher than the
analogous alkanes,
scaling with the
atomic weight...
-
preventing the
reformation of
disulfide linkages.
Halogen exchange to
produce iodoalkanes by the
Finkelstein reaction is
slightly complicated by the fact that...
- carbon–halogen bond. This bond can be
relatively weak (in the case of an
iodoalkane) or
quite stable (as in the case of a fluoroalkane). In general, with...
- in
demethylation of aryl
methyl ethers in DMF
under reflux condition.
Iodoalkanes Iodobenzene "B24840 Iodocyclohexane, 98%, stab. with copper". Alfa Aesar...
- aryl, and acyl
substituted cyclopropanes via
organometallic reactions.
Iodoalkanes "Iodocyclopropane".
Manchester Organics.
Retrieved 31 May 2023. "Iodocyclopropane"...
- any 540–760 weak to
medium bromoalkanes any 500–600
medium to
strong iodoalkanes any 500
medium to
strong N─O
nitro compounds aliphatic 1540 stronger...
- Iodomethane, also
called methyl iodide, and
commonly abbreviated "MeI", is the
chemical compound with the
formula CH3I. It is a dense, colorless, volatile...
-
Iodoform (also
known as triiodomethane) is the
organoiodine compound with the
chemical formula CHI3. It is a pale yellow, crystalline,
volatile substance...
-
reacts with
alkyl ethers (ROR′),
forming silyl ethers (ROSiMe3) and
iodoalkanes (RI) that can be
hydrolyzed to
alcohols (ROH).
Trimethylsilyl iodide...
