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About This Item
Empirical Formula (Hill Notation):
Os
CAS Number:
Molecular Weight:
190.23
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
11101711
EC Number:
231-114-0
MDL number:
InChI key
SYQBFIAQOQZEGI-UHFFFAOYSA-N
InChI
1S/Os
SMILES string
[Os]
assay
99.9% trace metals basis
form
powder
resistivity
8.12 μΩ-cm, 20°C
bp
5027 °C (lit.)
mp
3045 °C (lit.)
density
22.61 g/cm3 (lit.)
Quality Level
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
4.1B - Flammable solid hazardous materials
wgk
nwg
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves, type P3 (EN 143) respirator cartridges
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Isolda Romero-Canelón et al.
Journal of medicinal chemistry, 56(3), 1291-1300 (2013-02-02)
Organometallic half-sandwich complexes [M(p-cymene)(azo/imino-pyridine)X](+) where M = Ru(II) or Os(II) and X ═ Cl or I, exhibit potent antiproliferative activity toward a range of cancer cells. Not only are the iodido complexes more potent than the chlorido analogues, but they
Bastien Boff et al.
Inorganic chemistry, 52(5), 2705-2715 (2013-02-23)
A library of 29 organoosmium compounds has been built up with known and novel cyclometalated compounds obtained with C-N, N(∧)C(∧)N, and C(∧)N(∧)N ligands. All compounds have been tested for their in vitro cytotoxic properties against A172, a tumor cell line
Kilian Muñiz
Chemical Society reviews, 33(3), 166-174 (2004-03-18)
Imido complexes of osmium tetroxide are versatile compounds for olefin functionalisation. This tutorial review offers a brief historical overview on these compounds and discusses the electronic properties and reactivities of isolated imido osmium compounds in what had been the original
Hideki Sugimoto et al.
Journal of the American Chemical Society, 134(46), 19270-19280 (2012-11-02)
For the synthesis of the 1,2-diols, cis-1,2-dihydroxylation of alkenes catalyzed by osmium(VIII) tetroxide (OsO(4)) is a powerful method. However, OsO(4) is quite toxic due to its highly volatile and sublimable nature. Thus, the development of alternative catalysts for cis-1,2-dihydroxylation of
Michael H Stewart et al.
ACS nano, 6(6), 5330-5347 (2012-06-08)
The ability of luminescent semiconductor quantum dots (QDs) to engage in diverse energy transfer processes with organic dyes, light-harvesting proteins, metal complexes, and redox-active labels continues to stimulate interest in developing them for biosensing and light-harvesting applications. Within biosensing configurations
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