A22858
Acetylthiourea
99%
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About This Item
Linear Formula:
CH3CONHCSNH2
CAS Number:
Molecular Weight:
118.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-699-9
Beilstein/REAXYS Number:
969960
MDL number:
Assay:
99%
Form:
powder
InChI
1S/C3H6N2OS/c1-2(6)5-3(4)7/h1H3,(H3,4,5,6,7)
InChI key
IPCRBOOJBPETMF-UHFFFAOYSA-N
SMILES string
CC(=O)NC(N)=S
assay
99%
form
powder
mp
165-169 °C (lit.)
signalword
Danger
hcodes
pcodes
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 P2 (EN 143) respirator cartridges
Regulatory Information
危险化学品
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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
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
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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