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A22858

Sigma-Aldrich

Acetylthiourea

99%

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About This Item

Linear Formula:
CH3CONHCSNH2
CAS Number:
591-08-2
Molecular Weight:
118.16
Beilstein/REAXYS Number:
969960
EC Number:
209-699-9
MDL number:
MFCD00004937
UNSPSC Code:
12352100
PubChem Substance ID:
24890644
NACRES:
NA.22

assay

99%

form

powder

mp

165-169 °C (lit.)

SMILES string

CC(=O)NC(N)=S

InChI

1S/C3H6N2OS/c1-2(6)5-3(4)7/h1H3,(H3,4,5,6,7)

InChI key

IPCRBOOJBPETMF-UHFFFAOYSA-N

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pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H300

Hazard Classifications

Acute Tox. 2 Oral

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Olufunke Olagunju et al.
The journal of physical chemistry. A, 110(7), 2396-2410 (2006-02-17)
The oxidation reactions of N-acetylthiourea (ACTU) by chlorite and chlorine dioxide were studied in slightly acidic media. The ACTU-ClO(2)(-) reaction has a complex dependence on acid with acid catalysis in pH > 2 followed by acid retardation in higher acid
Chunlian Qin et al.
Talanta, 199, 131-139 (2019-04-07)
Detection and identification of bitter compounds draw great attention in pharmaceutical and food industry. Several well-known agonists of specific bitter taste receptors have been found to exhibit anti-cancer effects. For example, N-C=S-containing compounds, such as allyl-isothiocyanates, have shown cancer chemo-preventive
László Somogyi et al.
Carbohydrate research, 344(1), 134-135 (2008-11-04)
Treatment with concd HCl/MeOH transformed N-(tetra-O-acetyl-beta-D-glucopyranosyl)-N'-acetylthiourea, via selective cleavage of the primary alcoholic ester group, into the title compound.
V S Gudumak et al.
Laboratornoe delo, (9)(9), 15-18 (1989-01-01)
The authors have examined the possibility of replacing sodium arsenite with acetyl thiourea and of using butanol acidified with phosphoric acid in measuring sialic acids in biologic material. The results evidence a sufficient specificity, reproducibility, higher sensitivity and lower toxicity
Raushan K Singh et al.
Bioorganic & medicinal chemistry letters, 21(19), 5920-5923 (2011-08-26)
We report, for the first time, that certain N-acetylthiourea derivatives serve as highly potent and isozyme selective activators for the recombinant form of human histone deacetylase-8 in the assay system containing Fluor-de-Lys as a fluorescent substrate. The experimental data reveals

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