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Home  > Triruthenium dodecacarbonyl

AB51914

15243-33-1 | Triruthenium dodecacarbonyl

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $32.00 $22.00 -   +
1g 98% in stock $62.00 $44.00 -   +
5g >98% in stock $195.00 $136.00 -   +
25g 98% in stock $714.00 $500.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB51914
Chemical Name: Triruthenium dodecacarbonyl
CAS Number: 15243-33-1
Molecular Formula: C12O12Ru3
Molecular Weight: 639.3312
MDL Number: MFCD00011209
SMILES: [O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[O+]#[C-].[Ru].[Ru].[Ru]

 

Upstream Synthesis Route
  • Triruthenium dodecacarbonyl, also known as Ru3(CO)12, is a useful reagent in chemical synthesis due to its unique properties and reactivity. This complex organometallic compound consists of three ruthenium atoms bonded together with twelve carbonyl ligands.In chemical synthesis, Triruthenium dodecacarbonyl is commonly used as a source of ruthenium in various reactions. Its high solubility in a variety of solvents allows for easy manipulation in solution-phase reactions. This compound is particularly valuable in catalytic applications, where ruthenium's ability to undergo multiple oxidation states can facilitate a wide range of transformations.One prominent application of Triruthenium dodecacarbonyl is in the synthesis of organic molecules through carbonylation reactions. By serving as a carbon monoxide source, this compound enables the introduction of carbonyl groups into organic substrates, leading to the formation of a diverse array of functionalized products. Additionally, the reactivity of the ruthenium center allows for selective and efficient transformations, making it a versatile tool in organic synthesis.Overall, Triruthenium dodecacarbonyl plays a crucial role in modern chemical synthesis by providing a reliable source of ruthenium and enabling selective transformations through carbonylation reactions. Its broad applicability and reactivity make it a valuable reagent for the synthesis of complex organic molecules.
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