Merck
CN
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文件

263257

Sigma-Aldrich

锇

powder, 99.9% trace metals basis

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经验公式（希尔记法）:
Os
CAS号:
7440-04-2
分子量:
190.23
EC 号:
231-114-0
MDL编号:
MFCD00011147
PubChem化学物质编号:
24855959
NACRES:
NA.23

质量水平

100

检测方案

99.9% trace metals basis

形式

powder

电阻率

8.12 μΩ-cm, 20°C

bp

5027 °C (lit.)

mp

3045 °C (lit.)

密度

22.61 g/cm3 (lit.)

SMILES字符串

[Os]

InChI

1S/Os

InChI key

SYQBFIAQOQZEGI-UHFFFAOYSA-N

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相关类别

警示用语：

Danger

危险分类

Eye Dam. 1 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

4.1B - Flammable solid hazardous materials

WGK

nwg

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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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
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
Werner Ginzinger et al.
Journal of medicinal chemistry, 55(7), 3398-3413 (2012-03-16)
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Vladimir B Arion et al.
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A modified paullone ligand bearing a TEMPO free-radical unit (HL) and its ruthenium(II) and osmium(II)-arene complexes [M(p-cymene)(HL)Cl]Cl·nH(2)O (M = Ru, Os) exhibit high antiproliferative activity in human cancer cell lines.
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