595187
Lithium
~40 wt % dispersion in mineral oil
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About This Item
Linear Formula:
Li
CAS Number:
Molecular Weight:
6.94
EC Number:
231-102-5
UNSPSC Code:
12352000
MDL number:
InChI key
WHXSMMKQMYFTQS-UHFFFAOYSA-N
InChI
1S/Li
SMILES string
[Li]
reaction suitability
reagent type: reductant
concentration
~40 wt % dispersion in mineral oil
resistivity
9.446 μΩ-cm, 20°C
bp
1342 °C (lit.)
mp
180 °C (lit.)
density
0.534 g/mL at 25 °C (lit.)
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Enikö Zörgö et al.
PLoS genetics, 9(3), e1003388-e1003388 (2013-04-05)
The number of chromosome sets contained within the nucleus of eukaryotic organisms is a fundamental yet evolutionarily poorly characterized genetic variable of life. Here, we mapped the impact of ploidy on the mitotic fitness of baker's yeast and its never
Dongyun Chen et al.
Nanoscale, 5(17), 7890-7896 (2013-07-16)
Two-dimensional nanosheets can leverage on their open architecture to support facile insertion and removal of Li(+) as lithium-ion battery electrode materials. In this study, two two-dimensional nanosheets with complementary functions, namely nitrogen-doped graphene and few-layer WS2, were integrated via a
John R Geddes et al.
Lancet (London, England), 381(9878), 1672-1682 (2013-05-15)
We review recent developments in the acute and long-term treatment of bipolar disorder and identify promising future routes to therapeutic innovation. Overall, advances in drug treatment remain quite modest. Antipsychotic drugs are effective in the acute treatment of mania; their
Jian Jiang et al.
Nanoscale, 5(17), 8105-8113 (2013-07-26)
Controlled integration of multiple semiconducting oxides into each single unit of ordered nanotube arrays is highly desired in scientific research for the realization of more attractive applications. We herein report a diffusion-controlled solid-solid route to evolve simplex Co(CO3)0.5(OH)0.11H2O@TiO2 core-shell nanowire
Sureshbabu Guduguntla et al.
The Journal of organic chemistry, 78(17), 8274-8280 (2013-08-22)
An efficient one-pot synthesis of optically active β-alkyl-substituted alcohols through a tandem copper-catalyzed asymmetric allylic alkylation (AAA) with organolithium reagents and reductive ozonolysis is presented. Furthermore, hydroboration-oxidation following the Cu-catalyzed AAA leads to the corresponding homochiral γ-alkyl-substituted alcohols.
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