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PrimorTrace™, ≥99.999% metals basis PrimorTrace™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Argon charged Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product class
Electronic Materials, PGM based Electronic Materials
Chemical properties
C14H18Ru
Ru(EtCp)2
287.37
Ru
35
liquid
pale yellow
99.999
Applications & references
Precursor for Atomic Layer Deposition (ALD) of Ru and RuO2 thin films
High-yielding preparation of ezentimibe and derivatives thereof for the treatment of hypercholesterolemia within an asymmetric transfer hydrogenation.
Reference: WO2008 0899984
Asymmetric transfer hydrogenation step in the total synthesis of montekulast for its use as sodium salt.
Reference: WO2008 009970
Reduction of allylic alcohols in organic medium.
Reference: Green. Chem. 2009, 11, 1992 (DOI: 10.1039/B916117A)
Asymmetric transfer hydrogenation of fluoroalkyl ketones yielding the corresponding alcohols with high ee's and in excellent yields.
Reference: Org. Lett. 2006, 8, 5935 (DOI: 10.1021/ol062358r)
| Pubchem Sid | 504769150 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504769150 |
| Canonical Smiles | CCC1=[C-]CC=C1.CCC1=[C-]CC=C1.[Ru+2] |
| IUPAC Name | 2-ethylcyclopenta-1,3-diene;ruthenium(2+) |
| InChIKey | XUZWCRWRRXUMJF-UHFFFAOYSA-N |
| INCHI | 1S/2C7H9.Ru/c2*1-2-7-5-3-4-6-7;/h2*3,5H,2,4H2,1H3;/q2*-1;+2 |
| Isomeric SMILES | CCC1=[C-]CC=C1.CCC1=[C-]CC=C1.[Ru+2] |
| WGK Germany | 3 |
| Molecular Weight | 287.36 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Hydrocarbons |
| Class | Unsaturated hydrocarbons |
| Subclass | Branched unsaturated hydrocarbons |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Branched unsaturated hydrocarbons |
| Alternative Parents | Cycloalkenes Unsaturated aliphatic hydrocarbons Organic salts Hydrocarbon derivatives Organic cations |
| Molecular Framework | Not available |
| Substituents | Branched unsaturated hydrocarbon - Cycloalkene - Cyclic olefin - Unsaturated aliphatic hydrocarbon - Hydrocarbon derivative - Organic salt - Olefin - Organic cation - Aliphatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as branched unsaturated hydrocarbons. These are hydrocarbons that contains one or more unsaturated carbon atoms, and an aliphatic branch. |
| External Descriptors | Not available |
| Sensitivity | Moisture sensitive;Hygroscopic |
|---|---|
| Refractive Index | n20/D 1.5870 (lit.) |
| Flash Point(°F) | 199.9 °F - closed cup |
| Flash Point(°C) | > 93.3 °C - closed cup |
| Boil Point(°C) | 100 °C/0.01 mmHg (lit.) |
| Melt Point(°C) | 6 °C (lit.) |
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