-
Sulfinylmethane or
sulfine is an
organic compound with
molecular formula H2CSO. It is the
simplest sulfine.
Sulfines are
chemical compounds with the general...
-
class of
organosulfur compounds known as
thiocarbonyl S-oxides (formerly "
sulfines"), is a
volatile liquid that acts as a
lachrymatory agent (triggers tearing...
- S-dioxides or sulfenes, R2C=SO2). The
thione S-oxides have also been
known as
sulfines, and
while IUPAC considers this term obsolete, the name
persists in the...
- 107-13-1 H2CO
formaldehyde 19710-56-6 H2CO3
carbonic acid 107-32-4 H2CSO
sulfine 40100-16-1 H2C2O4
oxalic acid 144-62-7 H2C4H4O6
tartaric acid 87-69-4 H2C8H4O4...
- (1980). "Rearrangement of
penicillin sulfoxides in base. Penicillin-derived
sulfines".
Journal of the
American Chemical Society. 102 (26): 7815–7816. doi:10...
- m****: 61.9826 u) may
refer to:
Thioformic acid, a
thiocarboxylic acid
Sulfine (sulfinylmethane) This set
index page
lists chemical structure articles...
- CH2O
hydroxymethylene 19710-56-6 CH2O
polyoxymethylene 9002-81-7 CH2OS
sulfine 40100-16-1 CH2O2
dioxirane 157-26-6 CH2O2
formic acid 64-18-6 CH2O3 carbonic...
- of use in
organic synthesis for
reducing sulfoxides to thioethers, and
sulfines to thioketones. Greenwood,
Norman N.; Earnshaw, Alan (1997). Chemistry...
-
thioacyl chlorides.
Oxygen transfer to a
dithiocarboxylate ester gives a
sulfine-like S-oxide that
rearranges to an
acylsulfenyl thiolate. Grote, Johanna;...
- the
action of
alcoholic potash and
methyl iodide on
ethylidene diethyl sulfine, CH3CH(SO2C2H5)2 (which is
formed by the
oxidation of
dithioacetal with...
