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261262

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

Signal Word

Danger

Hazard Statements

H228

Precautionary Statements

P210

Hazard Classifications

Flam. Sol. 1

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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
Jacob S Kanady et al.
Journal of the American Chemical Society, 135(3), 1073-1082 (2012-12-18)
The oxygen-evolving complex (OEC) of photosystem II contains a Mn(4)CaO(n) catalytic site, in which reactivity of bridging oxidos is fundamental to OEC function. We synthesized structurally relevant cuboidal Mn(3)MO(n) complexes (M = Mn, Ca, Sc; n = 3,4) to enable
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