모든 사진(1)
About This Item
Linear Formula:
SCNCOOCH2CH3
CAS Number:
Molecular Weight:
131.15
Beilstein:
606091
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
98%
양식
liquid
refractive index
n20/D 1.500 (lit.)
bp
56 °C/18 mmHg (lit.)
density
1.112 g/mL at 25 °C (lit.)
작용기
amine
isothiocyanate
저장 온도
2-8°C
SMILES string
CCOC(=O)N=C=S
InChI
1S/C4H5NO2S/c1-2-7-4(6)5-3-8/h2H2,1H3
InChI key
BDTDECDAHYOJRO-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Ethoxycarbonyl isothiocyanate reacts with 2-amino-tetrahydrobenzo[b]thiophene derivatives to yield tetrahydrobenzo[b]thiophen-2-thiourea derivatives.
애플리케이션
Ethoxycarbonyl isothiocyanate has been used in the synthesis of:
- pyrazolo[1,5-a][1,3,5]triazine derivatives, potential inhibitors of protein kinase CK2
- fused thiophene derivatives, having antibacterial and antifungal activities
- 4-thiouracil derivatives
- thiocarbamides from stannylarenes
- 1,3,5-triazin-2-one-4-thiones from 2-amino-2-oxazolines
- N-acylthioureas from aminodeoxy sugars
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 3 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
122.0 °F - closed cup
Flash Point (°C)
50 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
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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