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Merck
CN

GF52166943

Samarium

foil, not light tested, 25x25mm, thickness 0.005mm, as rolled, 99%

Synonym(s):

Samarium, SM000205

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About This Item

Empirical Formula (Hill Notation):
Sm
CAS Number:
7440-19-9
Molecular Weight:
150.36
MDL number:
MFCD00011233
UNSPSC Code:
12141612
PubChem Substance ID:
329807881
NACRES:
NA.23

Key Documents

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Assay

99%

form

foil

manufacturer/tradename

Goodfellow 521-669-43

resistivity

91.4 μΩ-cm, 0°C

size × thickness

25x25 mm × 0.005 mm

bp

1794 °C (lit.)

mp

1074 °C (lit.)

density

7.47 g/mL at 25 °C (lit.)

SMILES string

[Sm]

InChI

1S/Sm

InChI key

KZUNJOHGWZRPMI-UHFFFAOYSA-N

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General description

For updated SDS information please visit www.goodfellow.com.

Legal Information

Product of Goodfellow

Pictograms

Flame
GHS02

Signal Word

Warning

Hazard Statements

H261

Hazard Classifications

Water-react 3

Storage Class Code

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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A N Serafini
Cancer, 88(12 Suppl), 2934-2939 (2000-07-18)
In patients with bone pain due to metastatic disease, intravenous systemic radioisotope therapy may be a useful adjunct to other methods for palliating pain. Various studies have been performed utilizing a short-lived radioisotope conjugated to a tetraphosphonate (samarium 153 lexidronam)
Jose M Concellón et al.
Chemical Society reviews, 33(9), 599-609 (2004-12-14)
The development of methodologies for the formation of carbon-carbon double bonds could be considered one of the most important challenges in organic synthesis. To this end, beta-elimination reactions in 1,2-difunctionalised substrates have been one of the most important means of
Y Kamochi et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 120(3), 245-255 (2000-03-21)
This review deals with the rapid reduction of a variety of organic functionalities, including a new selective reduction of carboxylic acid, with samarium diiodide in the presence of additives under mild conditions. The single electron donor ability of samarium diiodide
K C Nicolaou et al.
Angewandte Chemie (International ed. in English), 48(39), 7140-7165 (2009-08-29)
Introduced by Henri Kagan more than three decades ago, samarium diiodide (SmI(2)) has found increasing application in chemical synthesis. This single-electron reducing agent has been particularly useful in C-C bond formations, including those found in total synthesis endeavors. This Review
José M Concellón et al.
Chemical Society reviews, 39(11), 4103-4113 (2010-08-05)
Samarium metal and samarium diiodide have become important tools as selective cyclopropanating agents in organic synthesis due to their high chemo- and stereoselectivity. Therefore, Sm and SmI(2) are the ideal reagents to prepare cyclopropane derivatives. This tutorial review highlights C-C
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