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Merck
CN

196126

乙氧羰基异硫氰酸酯

98%

别名:

异硫氰酰甲酸乙酯

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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
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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

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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