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216186

Sigma-Aldrich

Potassium selenocyanate

reagent grade, 97%

Synonym(s):

Selenocyanic acid potassium

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10 G
$99.75
50 G
$385.00
250 G
$1,350.00

About This Item

Linear Formula:
KSeCN
CAS Number:
Molecular Weight:
144.08
Beilstein/REAXYS Number:
3912121
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23
assay:
97%
grade:
reagent grade
form:
solid

$99.75

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grade

reagent grade

Quality Level

assay

97%

form

solid

technique(s)

NMR: suitable

mp

100 °C

SMILES string

[K][Se]C#N

InChI

1S/CHNSe.K/c2-1-3;/h3H;/q;+1/p-1

InChI key

KYEKHFSRAXRJBR-UHFFFAOYSA-M

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General description

Potassium selenocyanate is a crystalline solid and a reagent for the conversion of alkyl halides to nitriles, and the production of pharmaceutical intermediates. It also finds application in the field of energy storage devices.[1][2]

Application

Potassium selenocyanate can be used as a:
  • Redox-active electrolyte to enhance the performance of carbon-based supercapacitors.[1]
  • Starting material for the one-pot stereoselective synthesis of alkyl styryl selenides.[2]
  • Precursor to synthesize Cu and Ni complexes with antioxidant/anti-inflammatory activities.[3]
  • Selenylating agent to prepare stereoselective selenoglycosides and selenium-linked disaccharides.[4]

signalword

Danger

Hazard Classifications

Acute Tox. 2 Oral - Acute Tox. 3 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Stereoselective synthesis of alkyl styryl selenides in one-pot: a straightforward approach by in situ dialkyl diselenide formation under transition metal-free conditions
Adrian A Heredia, et al.
Royal Society of Chemistry Advances, 5, 105699-105706 (2015)
Synthesis, structural characterization and antioxidant/anti-inflammatory activity of pentacoordinated bis(isoselenocyanato) and bis(isothiocyanato) CuII and NiII complexes with Me5dien: Crystal structure of [Cu(Me5dien)(NCSe)2]
Zacharias D. Georgousis, et al.
Journal of Molecular Structure, 837, 30-37 (2007)
Glycosyl selenoacetates: Versatile building blocks for the preparation of stereoselective selenoglycosides and selenium linked disaccharides
Tapasi Manna and Anup Kumar Misra
Organic & Biomolecular Chemistry, 17, 8902-8912 (2019)
Journal of the Chemical Society. Chemical Communications, 860-860 (1991)
J. Ind. Chem. Soc., 62, 800-800 (1985)

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