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About This Item
Linear Formula:
SeO2
CAS Number:
Molecular Weight:
110.96
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352303
EC Number:
231-194-7
MDL number:
vapor pressure
1 mmHg ( 157 °C)
assay
99.999% trace metals basis
form
solid
reaction suitability
core: selenium
mp
315 °C (subl.) (lit.)
SMILES string
O=[Se]=O
InChI
1S/O2Se/c1-3-2
InChI key
JPJALAQPGMAKDF-UHFFFAOYSA-N
Application
Mild oxidizing reagent for allylic olefins and acetylenes. Conversion of 1,3-diketones to 1,2,3-triones.
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signalword
Danger
hcodes
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
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Regulatory Information
危险化学品
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Articles
Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis
Tetrahedron Letters, 34, 2979-2979 (1993)
Asian Journal of Chemistry, 19, 4107-4107 (2007)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 204315-10G | 04061838766762 |
| 204315-50G | 04061838138231 |


