All Photos(1)
About This Item
Linear Formula:
C2H5NHCSNH2
CAS Number:
Molecular Weight:
104.17
Beilstein:
1699551
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
99%
form
solid
mp
108-110 °C (lit.)
solubility
methanol: soluble 25 mg/mL, clear, colorless
functional group
amine
thiourea
SMILES string
CCNC(N)=S
InChI
1S/C3H8N2S/c1-2-5-3(4)6/h2H2,1H3,(H3,4,5,6)
InChI key
GMEHFXXZSWDEDB-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
N-Ethylthiourea forms adduct with silver halides and their single crystal X-ray structural and spectroscopic characterizations are described.
Application
N-Ethylthiourea was used in the preparation of Re (III) complexes, which are precursors for the new rhenium complexes, potentially useful in nuclear medicine. It was also used in two-step protocol for the first chemoselective cleavage of 2-hydroxy acid amides.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Dinorah Gambino et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 58(14), 3085-3092 (2003-01-04)
Complexes of the type [Re(III)L6]X3, with L = thiourea, N-methylthiourea, N-ethylthiourea or N,N'-dimethytlthiourea and X = Cl- or PF6-, were prepared as suitable precursors for the synthesis of new rhenium complexes potentially useful in nuclear medicine. The infrared (IR) spectra
Erwin P Schreiner et al.
The Journal of organic chemistry, 67(24), 8299-8304 (2002-11-26)
A two-step protocol for the first chemoselective cleavage of 2-hydroxy acid amides has been developed. Mesylation of the model substrate 2-(hydroxypropionylamino)-4-methylpentanoic acid methyl ester (11) followed by treatment with N-ethylthiourea (13) allows cleavage of 2-hydroxy acid amides under smooth conditions.
Xutong Sun et al.
American journal of respiratory cell and molecular biology, 50(6), 1084-1095 (2014-01-08)
Recent studies have indicated that, during the development of pulmonary hypertension (PH), there is a switch from oxidative phosphorylation to glycolysis in the pulmonary endothelium. However, the mechanisms underlying this phenomenon have not been elucidated. Endothelin (ET)-1, an endothelial-derived vasoconstrictor
Graham A Bowmaker et al.
Dalton transactions (Cambridge, England : 2003), 39(18), 4391-4404 (2010-04-28)
Syntheses, single crystal X-ray structural and spectroscopic characterizations are described for a variety of adducts of silver halides with thiourea ('tu'), N-ethylthiourea ('ettu' = EtNH.CS.NH(2)) and N,N'-diethylthiourea ('detu' = EtNH.CS.EtNH). This study greatly extends our knowledge of the complex chemistry
M N Preobrazhenskaya et al.
The Journal of antibiotics, 44(2), 192-199 (1991-02-01)
A series of phenylthiourea and ethylthiourea derivatives of daunorubicin and its congeners was prepared by reaction of the 3'-amino group of the antibiotic with phenylisothiocyanate or ethylisothiocyanate. S-Methylation yielded S-methylisothiouromium salts which when reacted with amines resulted in an intramolecular
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service