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Merck

213365

Sigma-Aldrich

Selenium dioxide

ReagentPlus®, powder, 99.8% trace metals basis

Sinónimos:

NSC 56753, Selenium oxide

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About This Item

Fórmula lineal:
SeO2
Número de CAS:
Peso molecular:
110.96
EC Number:
MDL number:
UNSPSC Code:
12352303
PubChem Substance ID:
NACRES:
NA.23

vapor pressure

1 mmHg ( 157 °C)

Quality Level

product line

ReagentPlus®

assay

99.8% trace metals basis

form

powder

color

white

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. Conversion of 1,3-diketones to 1,2,3-triones

Other Notes

Material may contain dark crystals which are unavoidable and do not impact product quality

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

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


Certificados de análisis (COA)

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Visite la Librería de documentos

Tetrahedron Letters, 34, 2979-2979 (1993)
Asian Journal of Chemistry, 19, 4107-4107 (2007)
Zoyne Pedrero et al.
Journal of chromatography. A, 1139(2), 247-253 (2006-12-05)
Selenium speciation in Se-enriched Lens esculenta grown in hydroponic culture containing inorganic selenium as Na(2)SeO(3) and Na(2)SeO(4) was performed. After 16 days of growth, the plants were collected and divided in two parts, roots and stems and then analysed to
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
Erik A A Wallén et al.
Organic letters, 9(3), 389-391 (2007-01-26)
[reaction: see text] An efficient synthetic route to Cbz-protected 3-aminomethyl-2-aryl-8-bromo-6-chlorochromones has been developed. 3-Aryl-1-(3-bromo-5-chloro-2-hydroxyphenyl)-2-propen-1-one or 2-aryl-8-bromo-6-chlorochroman-4-one could be reacted under Mannich conditions yielding 2-aryl-8-bromo-6-chloro-3-methylenechroman-4-one, which was further converted to the target compound via an aza-Michael reaction followed by an SeO(2)

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