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223220
Thiocarbohydrazid
98%
Synonym(e):
Thiocarbonyldihydrazid
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About This Item
Lineare Formel:
(NH2NH)2CS
CAS-Nummer:
Molekulargewicht:
106.15
Beilstein:
506657
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
eCl@ss:
39093513
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Qualitätsniveau
Assay
98%
Form
solid
mp (Schmelzpunkt)
171-174 °C (dec.) (lit.)
Funktionelle Gruppe
amine
hydrazine
thiourea
SMILES String
NNC(=S)NN
InChI
1S/CH6N4S/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)
InChIKey
LJTFFORYSFGNCT-UHFFFAOYSA-N
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Anwendung
- Review of transition metal complexes with thiocarbohydrazides: This comprehensive review discusses the coordination chemistry of thiocarbohydrazides with various metals, highlighting their relevance in the synthesis of complex metal compounds used in catalysis and pharmaceutical research (Aly et al., 2023).
- Pd-doped nanocomposites for organometallic catalysis: Thiocarbohydrazide was employed in the fabrication of Pd-doped SBA-15 nanocomposites, applied as catalysts in the synthesis of organometallic compounds, showcasing its utility as a catalyst support material (Kalhor and Dadras, 2021).
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Acute Tox. 2 Oral
Lagerklassenschlüssel
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Kamaleddin Haj Mohammad Ebrahim Tehrani et al.
Iranian journal of pharmaceutical research : IJPR, 12(2), 331-346 (2013-11-20)
In this work, we reported the synthesis and evaluation of antimycobacterial and antifungal activity of a series of thiocarbohydrazone derivatives which are thiacetazone congeners. The target compounds were synthesized in superior yields by reacting thiocarbohydrazide with different aromatic aldehydes and
F Murata et al.
Journal of electron microscopy, 41(1), 14-20 (1992-02-01)
Sulfated glycoconjugates in epithelial cells and mesenchymal cells were investigated after staining with high iron diamine-thiocarbohydrazide-silver proteinate. One purpose of the experiment was to apply a new physical developed to the staining. Instead of silver nitrate, silver lactate or silver
M Goldberg et al.
European journal of oral sciences, 104(3), 269-277 (1996-06-01)
The appearance of the junction between predentin and dentin of rat incisors was investigated after chemical fixation (aldehyde), physical fixation (high pressure freezing and freeze substitution) and by histochemistry. Physical fixation revealed a 1-2 micron wide intermediary zone, in which
O Fujimori et al.
The Histochemical journal, 23(2), 91-99 (1991-02-01)
A method has been developed for the histochemical demonstration of unsaturated lipids in light microscopy. It is a peracetic acid-thiocarbohydrazide-silver protein sequence followed by a physical development procedure. In the present study on paraffin and cryostat sections of liver, brain
Debabrata Maity et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(40), 11152-11161 (2011-09-02)
We present novel Schiff base ligands julolidine-carbonohydrazone 1 and julolidine-thiocarbonohydrazone 2 for selective detection of Cu(2+) in aqueous medium. The planar julolidine-based ligands can sense Cu(2+) colorimetrically with characteristic absorbance in the near-infrared (NIR, 700-1000 nm) region. Employing molecular probes
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