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Merck
CN

V900086

Sigma-Aldrich

硫代乙酰胺

Vetec, reagent grade, 98%

别名:

乙硫酰胺

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About This Item

线性分子式:
CH3CSNH2
CAS号:
分子量:
75.13
Beilstein:
506006
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

等级

reagent grade

产品线

Vetec

检测方案

98%

mp

108-112 °C (lit.)

SMILES字符串

CC(N)=S

InChI

1S/C2H5NS/c1-2(3)4/h1H3,(H2,3,4)

InChI key

YUKQRDCYNOVPGJ-UHFFFAOYSA-N

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法律信息

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

象形图

Health hazardExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 1B - Eye Irrit. 2 - Skin Irrit. 2

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Hong Ling et al.
PloS one, 8(1), e54499-e54499 (2013-01-26)
Considerable evidence has demonstrated that transforming growth factor β (TGF-β) plays a key role in hepatic fibrosis, the final common pathway for a variety of chronic liver diseases leading to liver insufficiency. Although a few studies have reported that blocking
Peng Zhan et al.
Archives of pharmacal research, 35(6), 975-986 (2012-08-09)
In continuation of our endeavor to develop new, potent, selective and less toxic antiviral agents, a novel series of 2-(2-amino/chloro-4-(2,4-dibromophenyl) thiazol-5-ylthio)acetamide derivatives was synthesized via an expeditious route and evaluated for their anti-HIV activities against wild-type virus and clinically relevant
Chiung-Kuei Huang et al.
Hepatology (Baltimore, Md.), 57(4), 1550-1563 (2012-11-15)
Transplantation of bone marrow mesenchymal stem cells (BM-MSCs) has been considered as an alternative therapy, replacing liver transplantation in clinical trials, to treat liver cirrhosis, an irreversible disease that may eventually lead to liver cancer development. However, low survival rate
M Jamshidi et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 153, 257-267 (2015-09-01)
In this work, central composite design (CCD) combined with response surface methodology (RSM) and desirability function approach (DFA) gives useful information about operational condition and also to obtain useful information about interaction and main effect of variables concerned to simultaneous
Heather Hajovsky et al.
Chemical research in toxicology, 25(9), 1955-1963 (2012-08-08)
The hepatotoxicity of thioacetamide (TA) has been known since 1948. In rats, single doses cause centrolobular necrosis accompanied by increases in plasma transaminases and bilirubin. To elicit these effects, TA requires oxidative bioactivation, leading first to its S-oxide (TASO) and

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