- an
isothiourea, can be
encountered in
substituted compounds such as
isothiouronium salts. On the
other hand, some
compounds depicted as
isothioureas and...
- ICD-10 code for
Anthrax Chemical compound A22 (S-[3,4-dichlorobenzyl]
isothiourea hydrochloride) with
antibiotic activity A22
Sports Management, company...
-
phenylenediamine derivative (4).
Reaction of that
intermediate with S-methyl
isothiourea proceeds first by
aromatic cyclisation to the
guanidine derivative followed...
-
calculated as Keq is 1.04×10−3. The
thiol form,
which is also
known as an
isothiourea, can be
encountered in
substituted compounds such as
isothiouronium salts...
- S-(2-Aminoethyl)
isothiourea dihydrobromide,
commonly knwn as AET, is a isothiouronium-group-containing
reducing agent with
textbook uses as a disulfide...
-
asymmetric acyl
transfer on an
enantiomeric mixture catalyzed by a
chiral isothiourea. The acyl
group is
first transfer on to the
chiral catalyst which is...
- with the
formula [RSC(NH2)2]+ (R = alkyl, aryl) and is the acid salt of
isothiourea. The H
centres can also be
replaced by
alkyl and aryl. Structurally,...
-
amine featuring a
thiazole core. It can also be
considered a
cyclic isothiourea. It
possesses an odor
similar to
pyridine and is
soluble in water, alcohols...
- was
first prepared by
chemists at Ciba
Geigy in 1991. S-Methyl-N-nitro-
isothiourea is
treated with
methylamine to give N-methyl nitroguanidine. This intermediate...
- Alcohols, thiols, and
amines react analogously to give alkylisoureas,
isothioureas, and guanidines. The anti-ulcer drug
cimetidine is
generated using such...
