Cas 330983-72-7,[Ru(C6H5(CH2)3OH)(P(C6H11)3)H](1+)*BF4(1-)=[Ru(C6H5(CH2)3OH)(P(C6H11)3)H]BF4

330983-72-7

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Basic information

Product Name: [Ru(C₆H₅(CH₂)3OH)(P(C₆H₁₁)3)H]⁽¹⁺⁾*BF₄^(1-)=[Ru(C₆H₅(CH₂)3OH)(P(C₆H₁₁)3)H]BF₄
Synonyms:
CAS NO:330983-72-7
Molecular Formula:
Molecular Weight: 605.51
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(C₆H₅(CH₂)3OH)(P(C₆H₁₁)3)H]⁽¹⁺⁾*BF₄^(1-)=[Ru(C₆H₅(CH₂)3OH)(P(C₆H₁₁)3)H]BF₄(CAS DataBase Reference)
NIST Chemistry Reference: [Ru(C₆H₅(CH₂)3OH)(P(C₆H₁₁)3)H]⁽¹⁺⁾*BF₄^(1-)=[Ru(C₆H₅(CH₂)3OH)(P(C₆H₁₁)3)H]BF₄(330983-72-7)
EPA Substance Registry System: [Ru(C₆H₅(CH₂)3OH)(P(C₆H₁₁)3)H]⁽¹⁺⁾*BF₄^(1-)=[Ru(C₆H₅(CH₂)3OH)(P(C₆H₁₁)3)H]BF₄(330983-72-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 330983-72-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 330983-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,9,8 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 330983-72:
(8*3)+(7*3)+(6*0)+(5*9)+(4*8)+(3*3)+(2*7)+(1*2)=147
147 % 10 = 7
So 330983-72-7 is a valid CAS Registry Number.

330983-72-7Upstream product

330983-72-7Downstream Products

330983-72-7Relevant academic research and scientific papers

Co-catalyst dependent cycloisomerization or ring closing metathesis of α,ω-dienes catalyzed by arene ruthenium complex with side-arm alcohol

Miyaki, Yoshiharu,Onishi, Takafumi,Ogoshi, Sensuke,Kurosawa, Hideo

, p. 135 - 139 (2000)

Cycloisomerization and ring closing metathesis of some α,ω-dienes were catalyzed by a cationic arene ruthenium chelate complex [Ru{η6:η1-Ph(CH2) 3OH}(PCy3)Cl]BF4 (1a) in the presence of triethylamine and phenylacetylene, respectively, as co-catalysts. Analogous catalyst systems employing arene ruthenium cations without the side arm alcohol functional group showed lower efficiencies.

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