- In
organic chemistry, a
thial or
thioaldehyde is a
functional group which is
similar to an aldehyde, RC(O)H, in
which a
sulfur (S) atom
replaces the oxygen...
-
Names 2013. IUPAC–RSC. ISBN 978-0-85404-182-4. Zwanenburg, B. (2004). "
Thioaldehyde and
Thioketone S-Oxides and S-Imides (Sulfines and Derivatives)". In...
- the
organosulfur compound with the
formula CH2S. It is the
simplest thioaldehyde. This
compound is not
observed in the
condensed state (solid or liquid)...
-
uncommon with
alkyl substituents, but one
example is thiobenzophenone.
Thioaldehydes are
rarer still,
reflecting their lack of
steric protection ("thioformaldehyde"...
-
member of the sulfenes, the
group of
compounds which are S,S-dioxides of
thioaldehydes and thioketones, and have the
general formula R2C=SO2. The
first general...
-
Wisconsin Colleges,
accessed on line
August 4, 2007. §R-5.6.1, Aldehydes,
thioaldehydes, and
their analogues, A
Guide to
IUPAC Nomenclature of
Organic Compounds:...
-
Isocyanides −CN −NC cyano- isocyano- -nitrile*
isocyanide 5
Aldehydes Thioaldehydes −CHO −CHS formyl- thioformyl- -al* -thial* 6
Ketones Thioketones Selones...
-
remarquable que je
nomme stilbène." (On
submitting this
sulfide [i.e.,
phenyl thioaldehyde, C6H5(CS)H] to [dry] distillation, it
gives several products, and among...
-
Several 1,2-dithiolanes form S-oxides. S-oxides of
thioketones and
thioaldehydes,
compounds with the
formula R2C=S=O and RCH=S=O, respectively....
- thioenolates.
These structures exhibit tautomerism to give
thioketones or
thioaldehydes,
analogous to keto–enol
tautomerism of
carbonyl structures. Chiang,...
