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Merck
모든 사진(1)

주요 문서

163651

Sigma-Aldrich

Thioacetanilide

98%

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About This Item

Linear Formula:
CH3CSNHC6H5
CAS Number:
Molecular Weight:
151.23
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

98%

양식

powder

mp

76-79 °C (lit.)

작용기

amine

SMILES string

CC(=S)Nc1ccccc1

InChI

1S/C8H9NS/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)

InChI key

MWCGLTCRJJFXKR-UHFFFAOYSA-N

일반 설명

Metabolism and acute toxicity of thioacetanilide has been studied in rat[1]. Thioacetanilide undergoes nucleophilic addition reaction with superoxide ion in dimethyl sulfoxide[2].

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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문서 라이브러리 방문

Li-Rong Wen et al.
The Journal of organic chemistry, 73(5), 1852-1863 (2008-01-29)
A series of unusual fused tricyclic thiochromeno[2,3-b]pyridines were successfully synthesized by tandem [3 + 3] annulation and SNAr of beta-(2-chloroaroyl) thioacetanilides with activated 4-arylidene-2-phenyloxazol-5(4H)-ones or aromatic aldehydes and ethyl 2-cyanoacetate under microwave irradiation, respectively. Because of the existence of the
[Substantiation of maximum permissible levels of thioacylanilide in the air of work areas].
L G Aĭzvert et al.
Gigiena truda i professional'nye zabolevaniia, (7)(7), 51-52 (1986-07-01)
Reactivity of superoxide ion with thioamides in dimethyl sulfoxide.
Paez OA, et al.
The Journal of Organic Chemistry, 53(10), 2166-2170 (1988)
Toshiyuki Kitai et al.
Surgery today, 34(5), 424-428 (2004-04-27)
To assess the histological severity of liver cirrhosis in relation to the optical properties of liver tissue. Various grades of liver cirrhosis were induced in rats by giving intraperitoneal injections of thioacetamide (TAA) over periods ranging from 4 to 16
Xiao Li et al.
Bioorganic & medicinal chemistry, 20(18), 5527-5536 (2012-08-14)
In continuation of our efforts toward the discovery of potent HIV-1 NNRTIs with novel structures, we have employed a scaffold hopping strategy to explore the chemically diversed space of bioactive compounds. The original arylazolylthioacetanilide platform was replaced with different imidazopyridinylthioacetanilide

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