-
Thioanisole is an
organic compound with the
formula CH3SC6H5. It is a
colorless liquid that is
soluble in
organic solvents. It is the
simplest alkyl–aryl...
-
intermediate to
alkylate other nucleophiles;
scavengers such as
anisole or
thioanisole may be used.
Selective cleavage of the N-Boc
group in the
presence of...
- CH3S(O)C6H5. A low-melting
white solid, it is an
oxidized derivative of
thioanisole. The
compound is a
prototypical chiral sulfoxide. As such it has been...
- C7H8S (molar m****: 124.20 g/mol,
exact m****: 124.0347 u) may
refer to:
Thioanisole Benzyl mercaptan (phenylmethanethiol) This set
index page
lists chemical...
- is
oxidation of
thioethers to form sulfoxides, such as
conversion of
thioanisole to
methyl phenyl sulfoxide: Ph-S-CH3 + H2O2 → Ph-S(O)-CH3 + H2O Alkaline...
- example, C6H5SCH3 is
methyl phenyl sulfide, but is more
commonly called thioanisole,
since its
structure is
related to that for anisole, C6H5OCH3. The modern...
-
intermediate to
alkylate other nucleophiles;
scavengers such as
anisole or
thioanisole may be used.
Selective cleavage of the N-Boc
group in the
presence of...
-
gives methyl phenyl sulfide, C6H5SCH3, a
thioether often referred to as
thioanisole. Such
reactions are
fairly irreversible. C6H5SH also adds to α,β-unsaturated...
