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About This Item
Linear Formula:
CH3CSNHC6H5
CAS Number:
Molecular Weight:
151.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
form
powder
mp
76-79 °C (lit.)
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
General description
Metabolism and acute toxicity of thioacetanilide has been studied in rat. Thioacetanilide undergoes nucleophilic addition reaction with superoxide ion in dimethyl sulfoxide.
Signal Word
Warning
Hazard Statements
Precautionary Statements
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Anna Michta et al.
Acta crystallographica. Section C, Crystal structure communications, 64(Pt 8), o411-o413 (2008-08-07)
The title compound, C(8)H(9)NS, has four symmetry-independent molecules in the asymmetric unit. These molecules link into two independent infinite N-H...S hydrogen-bonded chains in the a-axis direction with graph-set notation C(2)(2)(8). The NH-CS group adopts a trans conformation and forms a
Peng Zhan et al.
Bioorganic & medicinal chemistry, 17(16), 5775-5781 (2009-08-01)
A series of 2-(1-aryl-1H-imidazol-2-ylthio)acetamide [imidazole thioacetanilide (ITA)] derivatives were synthesized and evaluated as potent inhibitors of human immunodeficiency virus type-1 (HIV-1). Among them, the most potent HIV-1 inhibitors were 4a5 (EC(50)=0.18microM), and 4a2 (EC(50)=0.20microM), which were more effective than the
Reactivity of superoxide ion with thioamides in dimethyl sulfoxide.
Paez OA, et al.
The Journal of Organic Chemistry, 53(10), 2166-2170 (1988)
[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)
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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