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GF01913419

Copper - O.F.H.C.

foil, 0.5m coil, thickness 0.006mm, hard, 99.95+%

Synonyme(s) :

Copper, CV000305

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About This Item

Formule empirique (notation de Hill):
Cu
Numéro CAS:
7440-50-8
Poids moléculaire :
63.55
Numéro MDL:
MFCD00010965
Code UNSPSC :
12141711
ID de substance PubChem :
329800286
Nomenclature NACRES :
NA.23

Essai

99.95%

Forme

foil

Fabricant/nom de marque

Goodfellow 019-134-19

Résistivité

1.673 μΩ-cm, 20°C

L × épaisseur

0.5 m × 0.006 mm

pb

2567 °C (lit.)

Pf

1083.4 °C (lit.)

Densité

8.94 g/mL at 25 °C (lit.)

Chaîne SMILES 

[Cu]

InChI

1S/Cu

Clé InChI

RYGMFSIKBFXOCR-UHFFFAOYSA-N

Description générale

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Informations légales

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Julie E Gleason et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(16), 5866-5871 (2014-04-09)
The human fungal pathogens Candida albicans and Histoplasma capsulatum have been reported to protect against the oxidative burst of host innate immune cells using a family of extracellular proteins with similarity to Cu/Zn superoxide dismutase 1 (SOD1). We report here
Alina Fedoseienko et al.
Annals of the New York Academy of Sciences, 1314, 6-14 (2014-04-05)
Copper is an important cofactor in numerous biological processes in all living organisms. However, excessive copper can be extremely toxic, so it is vital that the copper level within a cell is tightly regulated. The damaging effect of copper is
Adam Southon et al.
Metallomics : integrated biometal science, 5(10), 1346-1356 (2013-08-02)
Copper (Cu) is an essential redox active metal that is potentially toxic in excess. Multicellular organisms acquire Cu from the diet and must regulate uptake, storage, distribution and export of Cu at both the cellular and organismal levels. Systemic Cu
Gwilherm Evano et al.
Natural product reports, 30(12), 1467-1489 (2013-10-25)
Copper-catalyzed Ullmann-Goldberg-type cross-coupling reactions have undergone nothing short of a renaissance over the last decade and an impressive number of procedures are now available for the formation of C-N, C-O and C-S bonds with remarkable efficiencies and surgical precision. These
Lelita T Braiterman et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(14), E1364-E1373 (2014-04-08)
Wilson disease (WD) is a monogenic autosomal-recessive disorder of copper accumulation that leads to liver failure and/or neurological deficits. WD is caused by mutations in ATP7B, a transporter that loads Cu(I) onto newly synthesized cupro-enzymes in the trans-Golgi network (TGN)
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