163651
Thioacetanilide
98%
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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
Assay
98%
form
powder
mp
76-79 °C (lit.)
functional group
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
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
Regulatory Information
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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
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
Ester Muraglia et al.
Bioorganic & medicinal chemistry letters, 16(10), 2748-2752 (2006-03-01)
A series of aryltetrazolylacetanilides was synthesized and evaluated as HIV-1 non-nucleoside reverse transcriptase inhibitors on wild-type virus and on the clinically relevant K103N mutant strain. Extensive SAR investigation led to potent compounds, with nanomolar activity on K103N, and orally bioavailable
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
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
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