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About This Item
线性分子式:
SCNCOOCH2CH3
CAS号:
分子量:
131.15
Beilstein:
606091
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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化驗
98%
形狀
liquid
折射率
n20/D 1.500 (lit.)
bp
56 °C/18 mmHg (lit.)
密度
1.112 g/mL at 25 °C (lit.)
儲存溫度
2-8°C
SMILES 字串
CCOC(=O)N=C=S
InChI
1S/C4H5NO2S/c1-2-7-4(6)5-3-8/h2H2,1H3
InChI 密鑰
BDTDECDAHYOJRO-UHFFFAOYSA-N
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一般說明
Ethoxycarbonyl isothiocyanate reacts with 2-amino-tetrahydrobenzo[b]thiophene derivatives to yield tetrahydrobenzo[b]thiophen-2-thiourea derivatives.
應用
用于以甲锡烷基芳烃合成硫脲的通用试剂，从 2-氨基-2-噁唑啉制备 1,3,5-三嗪-2-酮-4-硫酮，以及用氨基脱氧糖合成 N-酰基硫脲。
訊號詞
Danger
危險分類
Acute Tox. 3 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
122.0 °F - closed cup
閃點（°C）
50 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
其他客户在看
A new synthesis of 4-thiouracils.
Lamon RW.
Journal of Heterocyclic Chemistry, 5, 837-844 (1968)
The Reaction of 2-Aminocyclohexeno [b] thiophene Derivatives with Ethoxycarbonyl isothiocyanate: Synthesis of Fused Thiophene Derivatives with Antibacterial and Antifungal Activities.
Wardakhan WW, et al.
Acta Chimica Slovenica, 54(2), 229-241 (2007)
Tetrahedron, 50, 3273-3273 (1994)
Zhe Nie et al.
Bioorganic & medicinal chemistry letters, 17(15), 4191-4195 (2007-06-02)
The structure-based design, synthesis, and anticancer activity of novel inhibitors of protein kinase CK2 are described. Using pyrazolo[1,5-a][1,3,5]triazine as the core scaffold, a structure-guided series of modifications provided pM inhibitors with microM-level cytotoxic activity in cell-based assays with prostate and
Heterocycles, 36, 2465-2465 (1993)
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