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204315

Sigma-Aldrich

Selenium dioxide

99.999% trace metals basis

Synonym(s):

NSC 56753, Selenium oxide

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10 G
$158.00
50 G
$594.00

About This Item

Linear Formula:
SeO2
CAS Number:
Molecular Weight:
110.96
EC Number:
MDL number:
UNSPSC Code:
12352303
PubChem Substance ID:
NACRES:
NA.23

$158.00


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vapor pressure

1 mmHg ( 157 °C)

Quality Level

assay

99.999% trace metals basis

form

solid

mp

315 °C (subl.) (lit.)

SMILES string

O=[Se]=O

InChI

1S/O2Se/c1-3-2

InChI key

JPJALAQPGMAKDF-UHFFFAOYSA-N

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Application

Mild oxidizing reagent for allylic olefins and acetylenes.[1] Conversion of 1,3-diketones to 1,2,3-triones.[2]

signalword

Danger

Hazard Classifications

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

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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Tetrahedron Letters, 34, 2979-2979 (1993)
Asian Journal of Chemistry, 19, 4107-4107 (2007)
Zhangrong Lou et al.
Chemical communications (Cambridge, England), 49(24), 2445-2447 (2013-02-19)
Based on a novel strategy for modulating the fluorescence of selenide and selenoxide, we have designed and developed a reversible fluorescent probe for hypochloric acid. And the synthesis, characterization, fluorescence properties, as well as the biological applications in living cells
Gary S Bañuelos et al.
Plant physiology, 155(1), 315-327 (2010-11-10)
The organ-specific accumulation, spatial distribution, and chemical speciation of selenium (Se) were previously unknown for any species of cactus. We investigated Se in Opuntia ficus-indica using inductively coupled plasma mass spectrometry, microfocused x-ray fluorescence elemental and chemical mapping (μXRF), Se
Vijay P Singh et al.
Chemistry, an Asian journal, 6(6), 1431-1442 (2011-05-11)
The syntheses of selenenate/seleninate esters and related derivatives by aromatic nucleophilic substitution (S(N)Ar) reactions of 2-bromo-3-nitrobenzylalcohol (13) and 2-bromo-3-nitrobenzaldehyde (17) with Na(2)Se(2)/nBuSeNa are described. The reaction of 13 with Na(2)Se(2) at room temperature afforded 7-nitro-1,2-benzisoselenole(3H) (15) instead of the desired

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Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis

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