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381411

Sigma-Aldrich

Triirondodecacarbonyl

greener alternative

contains 1-10% methyl alcohol

Synonym(s):

Dodecacarbonyltriiron, tri-Irondodecacarbonyl

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About This Item

Linear Formula:
Fe3(CO)12
CAS Number:
Molecular Weight:
503.66
MDL number:
UNSPSC Code:
12161600
PubChem Substance ID:
NACRES:
NA.22

contains

1-10% methyl alcohol

reaction suitability

core: iron
reagent type: catalyst

greener alternative product characteristics

Catalysis
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mp

165 °C (dec.) (lit.)

greener alternative category

storage temp.

2-8°C

SMILES string

[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].O=C1[Fe]23[Fe][Fe]12C3=O

InChI

1S/12CO.3Fe/c12*1-2;;;

InChI key

HLYRMDDXFDINCB-UHFFFAOYSA-N

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General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

Application

Eliminates sulfur from substituted thiophene complexes, leading to ferroles. Access to new areas of organometallic chemistry is promising using the reaction of Fe3(CO)12 with tellurium-nitrogen heterocycles such as benzoisotellurazole.

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Sol. 1

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 3

Flash Point(F)

49.5 °F - closed cup

Flash Point(C)

9.7 °C - closed cup


Certificates of Analysis (COA)

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Organometallics, 10, 1002-1002 (1991)
Badyal, K. et al.
Organometallics, 16, 3194-3194 (1997)
Weissensteiner,W.; Gutierrez, A. et al.
The Journal of Organic Chemistry, 50, 5822-5822 (1985)
Iranpoor, N.; Mottaghinejad, E.
Journal of Organometallic Chemistry, 423, 399-399 (1992)
Alper, H.; Gopal, M.
Journal of the Chemical Society. Chemical Communications, 821-821 (1980)

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