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223220

Thiocarbohydrazide

98%

Synonym(s):

Thiocarbonyldihydrazide

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About This Item

Linear Formula:
(NH2NH)2CS
CAS Number:
2231-57-4
Molecular Weight:
106.15
NACRES:
NA.22
PubChem Substance ID:
24853371
eCl@ss:
39093513
UNSPSC Code:
12352100
EC Number:
218-769-8
MDL number:
MFCD00007616
Beilstein/REAXYS Number:
506657
Assay:
98%
Form:
solid
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Quality Level

100

assay

98%

form

solid

mp

171-174 °C (dec.) (lit.)

functional group

amine, hydrazine, thiourea

SMILES string

NNC(=S)NN

InChI

1S/CH6N4S/c2-4-1(6)5-3/h2-3H2,(H2,4,5,6)

InChI key

LJTFFORYSFGNCT-UHFFFAOYSA-N

Application


  • 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).

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pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB8328
SDBB4869
STBL2996
STBK9373
STBK3832

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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
D P Singh et al.
Journal of enzyme inhibition and medicinal chemistry, 22(2), 177-182 (2007-05-24)
A novel series of complexes of the type [M(TML)X2]; where TML is Tetradentate Macrocyclic Ligand; M = Co(II), Ni(II), Cu(II), Zn(II)or Cd(II); X = Cl-, CH3COO- or NO3- have been synthesized by template condensation of glyoxal and thiocarbohydrazide in the
D Levanon et al.
The Histochemical journal, 31(1), 71-73 (1999-07-16)
Samples from seven sectors of the rabbit knee articular cartilage were shaved and prepared for the scanning electron microscope using either tannic acid, thiocarbohydrazide or nothing (control). Surface morphology was found to be more typical to a given sector and
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Global Trade Item Number

SKUGTIN
223220-5G04061838778253
223220-25G04061838778246