추천 제품
Quality Level
제품 라인
ReagentPlus®
분석
≥99.0%
양식
powder or crystals
pH
5.3-8.7 (25 °C, 97.2 g/L)
mp
173 °C (lit.)
SMILES string
[K]SC#N
InChI
1S/CHNS.K/c2-1-3;/h3H;/q;+1/p-1
InChI key
ZNNZYHKDIALBAK-UHFFFAOYSA-M
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관련 카테고리
일반 설명
Potassium thiocyanate (KSCN) is a potassium salt of thiocyanate anion. Its crystalline structure has been analyzed based on polarized infrared spectral data. The inhibition efficiency of KSCN dissolved in 1M HCl against the corrosion of carbon-steel has been evaluated. It facilitates the ring opening of aziridines with high regioselectivity.
애플리케이션
Potassium thiocyanate may be used in the synthesis of the following:
- α-Amino nitriles from tertiary amines.
- Polysubstituted 2-aminothiazoles from vinyl azides.
- Benzisothiazol-3(2H)-one derivatives from o-bromobenzamides.
- Diaryl thioethers from aryl halides.
법적 정보
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1
보충제 위험성
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
이미 열람한 고객
Regioselective ring-opening of aziridines with potassium thiocyanate in the presence of β-cyclodextrin in water.
Reddy MS, et al.
Tetrahedron Letters, 46(38), 6437-6439 (2005)
Synthesis of diaryl thioethers from aryl halides and potassium thiocyanate.
Hajipour AR, et al.
Applied Organometallic Chemistry, 28(12), 879-879 (2014)
Potassium Thiocyanate as Source of Cyanide for the Oxidative α-Cyanation of Tertiary Amines.
Wagner A and Ofial AR.
The Journal of Organic Chemistry, 80(5), 2848-2854 (2015)
Iron (II)-Promoted Synthesis of 2-Aminothiazoles via C=N Bond Formation from Vinyl Azides and Potassium Thiocyanate.
Zhang G, et al.
Advanced Synthesis & Catalysis, 357(5), 1065-1069 (2015)
Polarized infrared spectrum of potassium thiocyanate.
Jones LH.
J. Chem. Phys., 28(6), 1234-1236 (1958)
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