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アッセイ
99%
形状
foil
メーカー／製品名
Goodfellow 216-586-42
抵抗性
91.4 μΩ-cm, 0°C
サイズ×厚み
25 x 25 mm × 0.025 mm
bp
1794 °C (lit.)
mp
1074 °C (lit.)
密度
7.47 g/mL at 25 °C (lit.)
SMILES記法
[Sm]
InChI
1S/Sm
InChI Key
KZUNJOHGWZRPMI-UHFFFAOYSA-N
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詳細
For updated SDS information please visit www.goodfellow.com.
法的情報
Goodfellow製品
シグナルワード
Warning
危険有害性情報
危険有害性の分類
Water-react 3
保管分類コード
4.3 - Hazardous materials which set free flammable gases upon contact with water
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
GF21658642-5EA:
GF21658642-2EA:
GF21658642-1EA:
最新バージョンのいずれかを選択してください：
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)
Christine Beemelmanns et al.
Chemical Society reviews, 40(5), 2199-2210 (2011-01-19)
In this tutorial review we discuss recent advances in the field of ketyl-(het)arene cyclisations promoted by samarium diiodide and related processes. Couplings of samarium ketyls with carbon-carbon multiple bonds are perhaps the most useful reactions to create carbocycles and heterocycles
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
Hiroshi Suizu et al.
Organic letters, 17(1), 126-129 (2014-12-17)
A new synthetic route to clavilactone B, a naturally occurring inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase, is disclosed. The route features a sequential samarium-mediated radical cyclization-fragmentation of an indanone derivative, which provides rapid access to a 10-membered
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