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Sigma-Aldrich

Scandium

powder, 99.9% trace rare earth metals basis

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About This Item

Empirical Formula (Hill Notation):
Sc
CAS Number:
7440-20-2
Molecular Weight:
44.96
EC Number:
231-129-2
MDL number:
MFCD00016323
UNSPSC Code:
12141613
PubChem Substance ID:
24855801
NACRES:
NA.23

assay

99.9% trace rare earth metals basis

form

powder

resistivity

50.5 μΩ-cm, 0°C

bp

2836 °C (lit.)

mp

1540 °C (lit.)

density

2.99 g/mL at 25 °C (lit.)

SMILES string

[Sc]

InChI

1S/Sc

InChI key

SIXSYDAISGFNSX-UHFFFAOYSA-N

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Application

Employed in solid state synthesis of unusual clusters, Sc19Br28Z4, (Z=Mn, Fe, Ru or Os). These clusters are of interest for their structure and magnetic properties.

accessory

Product No.
Description
Pricing

pictograms

Flame
GHS02

signalword

Danger

hcodes

H228

pcodes

P210

Hazard Classifications

Flam. Sol. 1

Storage Class

4.1B - Flammable solid hazardous materials

wgk_germany

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

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Vincent Tran et al.
Organic letters, 14(23), 6100-6103 (2012-11-23)
Treatment of ynol ether-tethered dialkyl acetals with catalytic quantities of scandium triflate in CH(3)CN gives rise to five-, six-, and seven-membered alkoxycycloalkene carboxylates in good to excellent yields. Tri- and tetrasubstituted carbocyclic and heterocyclic alkenes may be formed by this
Marek Pruszyński et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 70(6), 974-979 (2012-04-03)
The positron-emitting radionuclide (44)Sc with a half-life of 3.97 h and a β(+) branching of 94.3% is of potential interest for clinical PET. As so far it is available from a (44)Ti/(44)Sc generator in Mainz, where long-lived (44)Ti decays to
Nadine V Hanhan et al.
Organic letters, 14(9), 2218-2221 (2012-04-18)
The scandium(III)-catalyzed enantioselective Hosomi-Sakurai allylation of isatins with various substituted allylic silanes is described. A catalyst loading as low as 0.05 mol % is utilized at room temperature to afford the 3-allyl-3-hydroxy-2-oxindoles in excellent yields and enantioselectivity up to 99%
Yunfei Cai et al.
Organic letters, 14(11), 2726-2729 (2012-05-17)
Catalytic asymmetric sulfenylation of unprotected 3-substituted oxindoles has been developed via cooperative catalysis of a chiral N,N'-dioxide-Sc(OTf)(3) complex and a Brønsted base. Utilizing readily available N-(phenylthio)phthalimide as the sulfur source, a wide range of optically active 3-phenylthiooxindoles were obtained in
Andrea Olmos et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(16), 4894-4901 (2012-03-15)
This study demonstrates the first zeolite-catalyzed synthesis of piperidine derivatives, including peptidomimetics and indoloquinolizidine alkaloids. The approach developed utilizes a highly effective one-pot reaction cascade, through imine formation and imino-Diels-Alder reactions, promoted by scandium-loaded zeolites as a heterogeneous catalyst. The
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