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线性分子式:
SCNCOOCH2CH3
化学文摘社编号:
分子量:
131.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
240-318-9
Beilstein/REAXYS Number:
606091
MDL number:
Assay:
98%
Form:
liquid
产品名称
乙氧羰基异硫氰酸酯, 98%
InChI key
BDTDECDAHYOJRO-UHFFFAOYSA-N
InChI
1S/C4H5NO2S/c1-2-7-4(6)5-3-8/h2H2,1H3
SMILES string
CCOC(=O)N=C=S
assay
98%
form
liquid
refractive index
n20/D 1.500 (lit.)
bp
56 °C/18 mmHg (lit.)
density
1.112 g/mL at 25 °C (lit.)
functional group
amine
isothiocyanate
storage temp.
2-8°C
Quality Level
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Application
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。
General description
Ethoxycarbonyl isothiocyanate reacts with 2-amino-tetrahydrobenzo[b]thiophene derivatives to yield tetrahydrobenzo[b]thiophen-2-thiourea derivatives.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
122.0 °F - closed cup
flash_point_c
50 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Tetrahedron, 50, 3273-3273 (1994)
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)
A new synthesis of 4-thiouracils.
Lamon RW.
Journal of Heterocyclic Chemistry, 5, 837-844 (1968)
Heterocycles, 36, 2465-2465 (1993)
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
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