Cas 109033-48-9,Ru(4+)*C5H5(1-)*HN(CH2CH2)2O*C4(C6H5)2H2(2-)*Br(1-)=((C5H5)Ru(HN(CH2CH2)2O)(C4(C6H5)2H2)Br)

109033-48-9

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Product Name: Ru⁽⁴⁺⁾*C₅H₅^(1-)*HN(CH₂CH₂)2O*C₄(C₆H₅)2H₂^(2-)*Br^(1-)=((C₅H₅)Ru(HN(CH₂CH₂)2O)(C₄(C₆H₅)2H₂)Br)
Synonyms:
CAS NO:109033-48-9
Molecular Formula:
Molecular Weight: 537.462
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Ru⁽⁴⁺⁾*C₅H₅^(1-)*HN(CH₂CH₂)2O*C₄(C₆H₅)2H₂^(2-)*Br^(1-)=((C₅H₅)Ru(HN(CH₂CH₂)2O)(C₄(C₆H₅)2H₂)Br)(CAS DataBase Reference)
NIST Chemistry Reference: Ru⁽⁴⁺⁾*C₅H₅^(1-)*HN(CH₂CH₂)2O*C₄(C₆H₅)2H₂^(2-)*Br^(1-)=((C₅H₅)Ru(HN(CH₂CH₂)2O)(C₄(C₆H₅)2H₂)Br)(109033-48-9)
EPA Substance Registry System: Ru⁽⁴⁺⁾*C₅H₅^(1-)*HN(CH₂CH₂)2O*C₄(C₆H₅)2H₂^(2-)*Br^(1-)=((C₅H₅)Ru(HN(CH₂CH₂)2O)(C₄(C₆H₅)2H₂)Br)(109033-48-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 109033-48-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109033-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,0,3 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109033-48:
(8*1)+(7*0)+(6*9)+(5*0)+(4*3)+(3*3)+(2*4)+(1*8)=99
99 % 10 = 9
So 109033-48-9 is a valid CAS Registry Number.

109033-48-9Upstream product

110-91-8 morpholine

109033-48-9Downstream Products

109033-48-9Relevant academic research and scientific papers

The Novel Cyclodimerization of Phenylacetylene at a Ruthenium(II) Centre. The Synthesis and X-Ray Structural Characterization of the First Metallacyclopentatriene, , and its Facile Conversion into Metallacyclopentadienes

Albers, Michel O.,Waal, Dirk J. A. de,Liles, David C.,Robinson, David J.,Singleton, Eric,Wiege, Manfred B.

, p. 1680 - 1682 (1986)

Cyclodimerization of two molecules of phenylacetylene at the ruthenium(II) centre in (C8H12 = cyclo-octa-1,5-diene) gives the novel ruthenacyclopentatriene characterized by 1H and 13H n.m.r. spectroscopy and by X-ray analysis; the triene undergoes facile 'oxidative addition' with donor ligands L (e.g. morpholine, trimethyl phosphite, dimethylphenylphosphine) in a bimolecular reaction involving an associative mode of activation to give the ruthenacyclopentadienes .

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