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Merck
CN

A22858

Sigma-Aldrich

乙酰硫脲

99%

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About This Item

线性分子式:
CH3CONHCSNH2
CAS号:
分子量:
118.16
Beilstein:
969960
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

99%

表单

powder

mp

165-169 °C (lit.)

SMILES字符串

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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象形图

Skull and crossbones

警示用语:

Danger

危险声明

预防措施声明

危险分类

Acute Tox. 2 Oral

储存分类代码

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

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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