推薦產品
化驗
98%
形狀
powder
mp
76-79 °C (lit.)
官能基
amine
SMILES 字串
CC(=S)Nc1ccccc1
InChI
1S/C8H9NS/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)
InChI 密鑰
MWCGLTCRJJFXKR-UHFFFAOYSA-N
訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
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
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
Reactivity of superoxide ion with thioamides in dimethyl sulfoxide.
Paez OA, et al.
The Journal of Organic Chemistry, 53(10), 2166-2170 (1988)
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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